Recall events
/
Event 68717
Event summary
Timeline bucket July 03, 2014
Product types Food
Classifications Class II
Statuses Terminated
Recalling firm wording GM Manufacturing Inc.
Dossier provenance
Source snapshots represented here
openFDA Food Enforcement
Report-date coverage
June 20, 2012–July 08, 2026
Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.
How coverage and grouping work
Device root-cause evidence is not applicable to this event.
No grouped product has the official product type device; this is not an unavailable-enrichment finding.
Complete imported group
Every recalled product in this event
46 official enforcement rows
Product dates, classifications, firms, and source wording remain attached to their individual rows.
Opening this dossier never hides products that did not match a prior timeline filter.
food · product 1 of 46
Tiger-X, Blister Packs
F-2242-2014
Recall number F-2242-2014
Initiated July 03, 2014
Classification Class II
Status Terminated
Quantity 11,218 units
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
violations of the cGMP
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall GM Manufacturing is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.
Code information No lot numbers
Official fact provenance
Dataset openFDA Food Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 ccbd901395e7f97453ba67323214b452ee901a828cb9048da8cb62e875bf39dc
Raw source locator 0001-food-enforcement-0001-of-0001.json.zip#results[5802]
FDA event record
· Exact recall-number query on openFDA
food · product 2 of 46
Samurai-X, Blister Packs
F-2243-2014
Recall number F-2243-2014
Initiated July 03, 2014
Classification Class II
Status Terminated
Quantity 21,394 units
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
violations of the cGMP
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall GM Manufacturing is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.
Code information No lot numbers
Official fact provenance
Dataset openFDA Food Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 ccbd901395e7f97453ba67323214b452ee901a828cb9048da8cb62e875bf39dc
Raw source locator 0001-food-enforcement-0001-of-0001.json.zip#results[5309]
FDA event record
· Exact recall-number query on openFDA
food · product 3 of 46
Samurai Gold, Blister Packs
F-2244-2014
Recall number F-2244-2014
Initiated July 03, 2014
Classification Class II
Status Terminated
Quantity 3,500 units
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
violations of the cGMP
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall GM Manufacturing is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.
Code information No lot numbers
Official fact provenance
Dataset openFDA Food Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 ccbd901395e7f97453ba67323214b452ee901a828cb9048da8cb62e875bf39dc
Raw source locator 0001-food-enforcement-0001-of-0001.json.zip#results[3974]
FDA event record
· Exact recall-number query on openFDA
food · product 4 of 46
Gold, Blister Packs
F-2245-2014
Recall number F-2245-2014
Initiated July 03, 2014
Classification Class II
Status Terminated
Quantity 5,039 units
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
violations of the cGMP
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall GM Manufacturing is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.
Code information No lot numbers
Official fact provenance
Dataset openFDA Food Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 ccbd901395e7f97453ba67323214b452ee901a828cb9048da8cb62e875bf39dc
Raw source locator 0001-food-enforcement-0001-of-0001.json.zip#results[3998]
FDA event record
· Exact recall-number query on openFDA
food · product 5 of 46
Oyavon, Blister Packs
F-2246-2014
Recall number F-2246-2014
Initiated July 03, 2014
Classification Class II
Status Terminated
Quantity 3,404 units
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
violations of the cGMP
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall GM Manufacturing is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.
Code information No lot numbers
Official fact provenance
Dataset openFDA Food Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 ccbd901395e7f97453ba67323214b452ee901a828cb9048da8cb62e875bf39dc
Raw source locator 0001-food-enforcement-0001-of-0001.json.zip#results[1581]
FDA event record
· Exact recall-number query on openFDA
food · product 6 of 46
Adam, Blister Packs
F-2247-2014
Recall number F-2247-2014
Initiated July 03, 2014
Classification Class II
Status Terminated
Quantity 9,500 units
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
violations of the cGMP
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall GM Manufacturing is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.
Code information No lot numbers
Official fact provenance
Dataset openFDA Food Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 ccbd901395e7f97453ba67323214b452ee901a828cb9048da8cb62e875bf39dc
Raw source locator 0001-food-enforcement-0001-of-0001.json.zip#results[5274]
FDA event record
· Exact recall-number query on openFDA
food · product 7 of 46
Actimeta, Blister Packs
F-2248-2014
Recall number F-2248-2014
Initiated July 03, 2014
Classification Class II
Status Terminated
Quantity 5,104 units
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
violations of the cGMP
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall GM Manufacturing is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.
Code information No lot numbers
Official fact provenance
Dataset openFDA Food Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 ccbd901395e7f97453ba67323214b452ee901a828cb9048da8cb62e875bf39dc
Raw source locator 0001-food-enforcement-0001-of-0001.json.zip#results[3980]
FDA event record
· Exact recall-number query on openFDA
food · product 8 of 46
Affirm XL, Blister Packs
F-2249-2014
Recall number F-2249-2014
Initiated July 03, 2014
Classification Class II
Status Terminated
Quantity 4,000 units
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
violations of the cGMP
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall GM Manufacturing is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.
Code information No lot numbers
Official fact provenance
Dataset openFDA Food Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 ccbd901395e7f97453ba67323214b452ee901a828cb9048da8cb62e875bf39dc
Raw source locator 0001-food-enforcement-0001-of-0001.json.zip#results[2480]
FDA event record
· Exact recall-number query on openFDA
food · product 9 of 46
Platinum A, Blister Packs
F-2250-2014
Recall number F-2250-2014
Initiated July 03, 2014
Classification Class II
Status Terminated
Quantity 6,250 units
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
violations of the cGMP
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall GM Manufacturing is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.
Code information No lot numbers
Official fact provenance
Dataset openFDA Food Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 ccbd901395e7f97453ba67323214b452ee901a828cb9048da8cb62e875bf39dc
Raw source locator 0001-food-enforcement-0001-of-0001.json.zip#results[6954]
FDA event record
· Exact recall-number query on openFDA
food · product 10 of 46
Platinum B, Blister Packs
F-2251-2014
Recall number F-2251-2014
Initiated July 03, 2014
Classification Class II
Status Terminated
Quantity 5,000 units
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
violations of the cGMP
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall GM Manufacturing is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.
Code information No lot numbers
Official fact provenance
Dataset openFDA Food Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 ccbd901395e7f97453ba67323214b452ee901a828cb9048da8cb62e875bf39dc
Raw source locator 0001-food-enforcement-0001-of-0001.json.zip#results[5259]
FDA event record
· Exact recall-number query on openFDA
food · product 11 of 46
Ninja Mojo, small vinyl Packs
F-2252-2014
Recall number F-2252-2014
Initiated July 03, 2014
Classification Class II
Status Terminated
Quantity 50,000 units
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
violations of the cGMP
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall GM Manufacturing is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.
Code information LOT08152013 EXPDEC2016
Official fact provenance
Dataset openFDA Food Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 ccbd901395e7f97453ba67323214b452ee901a828cb9048da8cb62e875bf39dc
Raw source locator 0001-food-enforcement-0001-of-0001.json.zip#results[6355]
FDA event record
· Exact recall-number query on openFDA
food · product 12 of 46
Single Mojo, small vinyl Packs
F-2253-2014
Recall number F-2253-2014
Initiated July 03, 2014
Classification Class II
Status Terminated
Quantity 45,000 units
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
violations of the cGMP
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall GM Manufacturing is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.
Code information LOT08162013 EXPDEC2016
Official fact provenance
Dataset openFDA Food Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 ccbd901395e7f97453ba67323214b452ee901a828cb9048da8cb62e875bf39dc
Raw source locator 0001-food-enforcement-0001-of-0001.json.zip#results[5810]
FDA event record
· Exact recall-number query on openFDA
food · product 13 of 46
Double Mojo, small vinyl Packs
F-2254-2014
Recall number F-2254-2014
Initiated July 03, 2014
Classification Class II
Status Terminated
Quantity 40,000 units
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
violations of the cGMP
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall GM Manufacturing is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.
Code information LOT08172013 EXPDEC2016
Official fact provenance
Dataset openFDA Food Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 ccbd901395e7f97453ba67323214b452ee901a828cb9048da8cb62e875bf39dc
Raw source locator 0001-food-enforcement-0001-of-0001.json.zip#results[5302]
FDA event record
· Exact recall-number query on openFDA
food · product 14 of 46
Ginseng Power, Blister Packs
F-2255-2014
Recall number F-2255-2014
Initiated July 03, 2014
Classification Class II
Status Terminated
Quantity 3,025 units
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
violations of the cGMP
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall GM Manufacturing is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.
Code information No Lot numbers
Official fact provenance
Dataset openFDA Food Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 ccbd901395e7f97453ba67323214b452ee901a828cb9048da8cb62e875bf39dc
Raw source locator 0001-food-enforcement-0001-of-0001.json.zip#results[6920]
FDA event record
· Exact recall-number query on openFDA
food · product 15 of 46
Calcium Formula, 250 cc HDPE Bottles
F-2256-2014
Recall number F-2256-2014
Initiated July 03, 2014
Classification Class II
Status Terminated
Quantity 501 units
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
violations of the cGMP
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall GM Manufacturing is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.
Code information EXP08.2016
Official fact provenance
Dataset openFDA Food Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 ccbd901395e7f97453ba67323214b452ee901a828cb9048da8cb62e875bf39dc
Raw source locator 0001-food-enforcement-0001-of-0001.json.zip#results[1584]
FDA event record
· Exact recall-number query on openFDA
food · product 16 of 46
Green Coffee Bean
F-2257-2014
Recall number F-2257-2014
Initiated July 03, 2014
Classification Class II
Status Terminated
Quantity 1,110 units
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
violations of the cGMP
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall GM Manufacturing is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.
Code information EXP08.2016 EXP10.2016
Official fact provenance
Dataset openFDA Food Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 ccbd901395e7f97453ba67323214b452ee901a828cb9048da8cb62e875bf39dc
Raw source locator 0001-food-enforcement-0001-of-0001.json.zip#results[1595]
FDA event record
· Exact recall-number query on openFDA
food · product 17 of 46
Shark Formula, 250 cc HDPE Bottles
F-2258-2014
Recall number F-2258-2014
Initiated July 03, 2014
Classification Class II
Status Terminated
Quantity 1,503 units
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
violations of the cGMP
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall GM Manufacturing is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.
Code information EXP10.2016 EXP11.2016 EXP12.2016
Official fact provenance
Dataset openFDA Food Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 ccbd901395e7f97453ba67323214b452ee901a828cb9048da8cb62e875bf39dc
Raw source locator 0001-food-enforcement-0001-of-0001.json.zip#results[5280]
FDA event record
· Exact recall-number query on openFDA
food · product 18 of 46
Bitter Melon, 225cc HDPE Bottle
F-2259-2014
Recall number F-2259-2014
Initiated July 03, 2014
Classification Class II
Status Terminated
Quantity 380 units
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
violations of the cGMP
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall GM Manufacturing is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.
Code information EXP10.2016
Official fact provenance
Dataset openFDA Food Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 ccbd901395e7f97453ba67323214b452ee901a828cb9048da8cb62e875bf39dc
Raw source locator 0001-food-enforcement-0001-of-0001.json.zip#results[5806]
FDA event record
· Exact recall-number query on openFDA
food · product 19 of 46
Chanca Piedra, 225cc HDPE Bottles
F-2260-2014
Recall number F-2260-2014
Initiated July 03, 2014
Classification Class II
Status Terminated
Quantity 378 units
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
violations of the cGMP
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall GM Manufacturing is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.
Code information EXP10.2016
Official fact provenance
Dataset openFDA Food Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 ccbd901395e7f97453ba67323214b452ee901a828cb9048da8cb62e875bf39dc
Raw source locator 0001-food-enforcement-0001-of-0001.json.zip#results[3983]
FDA event record
· Exact recall-number query on openFDA
food · product 20 of 46
Rinozan, 250cc HDPE Bottles
F-2261-2014
Recall number F-2261-2014
Initiated July 03, 2014
Classification Class II
Status Terminated
Quantity 501 units
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
violations of the cGMP
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall GM Manufacturing is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.
Code information EXP09.2016
Official fact provenance
Dataset openFDA Food Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 ccbd901395e7f97453ba67323214b452ee901a828cb9048da8cb62e875bf39dc
Raw source locator 0001-food-enforcement-0001-of-0001.json.zip#results[5291]
FDA event record
· Exact recall-number query on openFDA
food · product 21 of 46
Una De Gato, 225cc HDPE Bottle
F-2262-2014
Recall number F-2262-2014
Initiated July 03, 2014
Classification Class II
Status Terminated
Quantity 502 units
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
violations of the cGMP
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall GM Manufacturing is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.
Code information EXP12.2016
Official fact provenance
Dataset openFDA Food Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 ccbd901395e7f97453ba67323214b452ee901a828cb9048da8cb62e875bf39dc
Raw source locator 0001-food-enforcement-0001-of-0001.json.zip#results[6917]
FDA event record
· Exact recall-number query on openFDA
food · product 22 of 46
Saw Palmetto, Glass Bottle
F-2263-2014
Recall number F-2263-2014
Initiated July 03, 2014
Classification Class II
Status Terminated
Quantity 501 units
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
violations of the cGMP
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall GM Manufacturing is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.
Code information EXP11.2016
Official fact provenance
Dataset openFDA Food Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 ccbd901395e7f97453ba67323214b452ee901a828cb9048da8cb62e875bf39dc
Raw source locator 0001-food-enforcement-0001-of-0001.json.zip#results[6907]
FDA event record
· Exact recall-number query on openFDA
food · product 23 of 46
Garcinia Cambogia, 225cc HDPE Bottle
F-2264-2014
Recall number F-2264-2014
Initiated July 03, 2014
Classification Class II
Status Terminated
Quantity 829 units
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
violations of the cGMP
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall GM Manufacturing is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.
Code information EXP04.2017
Official fact provenance
Dataset openFDA Food Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 ccbd901395e7f97453ba67323214b452ee901a828cb9048da8cb62e875bf39dc
Raw source locator 0001-food-enforcement-0001-of-0001.json.zip#results[3978]
FDA event record
· Exact recall-number query on openFDA
food · product 24 of 46
BTI Lean Formula, 400cc HDPE Bottle
F-2265-2014
Recall number F-2265-2014
Initiated July 03, 2014
Classification Class II
Status Terminated
Quantity 1,000 units
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
violations of the cGMP
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall GM Manufacturing is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.
Code information LT7345 EX10.16
Official fact provenance
Dataset openFDA Food Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 ccbd901395e7f97453ba67323214b452ee901a828cb9048da8cb62e875bf39dc
Raw source locator 0001-food-enforcement-0001-of-0001.json.zip#results[3986]
FDA event record
· Exact recall-number query on openFDA
food · product 25 of 46
DMSA, 100cc HDPE bottle
F-2266-2014
Recall number F-2266-2014
Initiated July 03, 2014
Classification Class II
Status Terminated
Quantity 414 units
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
violations of the cGMP
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall GM Manufacturing is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.
Code information LOTKZ8010 EXP10.2016
Official fact provenance
Dataset openFDA Food Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 ccbd901395e7f97453ba67323214b452ee901a828cb9048da8cb62e875bf39dc
Raw source locator 0001-food-enforcement-0001-of-0001.json.zip#results[5816]
FDA event record
· Exact recall-number query on openFDA
food · product 26 of 46
Noni Supplement, Capsules
F-2267-2014
Recall number F-2267-2014
Initiated July 03, 2014
Classification Class II
Status Terminated
Quantity 200,100 units
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
violations of the cGMP
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall GM Manufacturing is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.
Code information 9/23/13 > 9/30/13
Official fact provenance
Dataset openFDA Food Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 ccbd901395e7f97453ba67323214b452ee901a828cb9048da8cb62e875bf39dc
Raw source locator 0001-food-enforcement-0001-of-0001.json.zip#results[5336]
FDA event record
· Exact recall-number query on openFDA
food · product 27 of 46
Therapeutic Care A, B, C, 225cc HDPE Bottles for A,B. Capsules for C
F-2268-2014
Recall number F-2268-2014
Initiated July 03, 2014
Classification Class II
Status Terminated
Quantity 168,874 units
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
violations of the cGMP
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall GM Manufacturing is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.
Code information LOTKZ1350, EXP11/2016 LOT KZ1351, EXP11/2016 LOTKZ1352, EXP11/2016
Official fact provenance
Dataset openFDA Food Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 ccbd901395e7f97453ba67323214b452ee901a828cb9048da8cb62e875bf39dc
Raw source locator 0001-food-enforcement-0001-of-0001.json.zip#results[4007]
FDA event record
· Exact recall-number query on openFDA
food · product 28 of 46
Actra-SX, Vinyl Bags
F-2269-2014
Recall number F-2269-2014
Initiated July 03, 2014
Classification Class II
Status Terminated
Quantity 188 units
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
violations of the cGMP
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall GM Manufacturing is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.
Official fact provenance
Dataset openFDA Food Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 ccbd901395e7f97453ba67323214b452ee901a828cb9048da8cb62e875bf39dc
Raw source locator 0001-food-enforcement-0001-of-0001.json.zip#results[4128]
FDA event record
· Exact recall-number query on openFDA
food · product 29 of 46
Maxium, Capsules; Prolong, Capsules
F-2270-2014
Recall number F-2270-2014
Initiated July 03, 2014
Classification Class II
Status Terminated
Quantity 62,280 units
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
violations of the cGMP
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall GM Manufacturing is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.
Code information 11/1/13 > 11/15/13
Official fact provenance
Dataset openFDA Food Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 ccbd901395e7f97453ba67323214b452ee901a828cb9048da8cb62e875bf39dc
Raw source locator 0001-food-enforcement-0001-of-0001.json.zip#results[6353]
FDA event record
· Exact recall-number query on openFDA
food · product 30 of 46
Serrapeptase, 100cc HDPE Bottles
F-2271-2014
Recall number F-2271-2014
Initiated July 03, 2014
Classification Class II
Status Terminated
Quantity 801 units
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
violations of the cGMP
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall GM Manufacturing is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.
Code information LOTKZ1320 EXPFEB2016
Official fact provenance
Dataset openFDA Food Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 ccbd901395e7f97453ba67323214b452ee901a828cb9048da8cb62e875bf39dc
Raw source locator 0001-food-enforcement-0001-of-0001.json.zip#results[4105]
FDA event record
· Exact recall-number query on openFDA
food · product 31 of 46
Garcinia Series, Capsules
F-2272-2014
Recall number F-2272-2014
Initiated July 03, 2014
Classification Class II
Status Terminated
Quantity 30,600 units
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
violations of the cGMP
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall GM Manufacturing is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.
Code information 4/9/14 > 4/12/14
Official fact provenance
Dataset openFDA Food Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 ccbd901395e7f97453ba67323214b452ee901a828cb9048da8cb62e875bf39dc
Raw source locator 0001-food-enforcement-0001-of-0001.json.zip#results[5798]
FDA event record
· Exact recall-number query on openFDA
food · product 32 of 46
Mega Jex, Capsules
F-2273-2014
Recall number F-2273-2014
Initiated July 03, 2014
Classification Class II
Status Terminated
Quantity 51,120 units
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
violations of the cGMP
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall GM Manufacturing is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.
Code information 12/11/12 > 12/12/12 4/30/13 > 5/1/13 12/13/13 > 12/17/13
Official fact provenance
Dataset openFDA Food Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 ccbd901395e7f97453ba67323214b452ee901a828cb9048da8cb62e875bf39dc
Raw source locator 0001-food-enforcement-0001-of-0001.json.zip#results[6958]
FDA event record
· Exact recall-number query on openFDA
food · product 33 of 46
Chitosan, Blister Pack
F-2274-2014
Recall number F-2274-2014
Initiated July 03, 2014
Classification Class II
Status Terminated
Quantity 2,010 units
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
violations of the cGMP
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall GM Manufacturing is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.
Code information 7/9/12 > 7/11/12
Official fact provenance
Dataset openFDA Food Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 ccbd901395e7f97453ba67323214b452ee901a828cb9048da8cb62e875bf39dc
Raw source locator 0001-food-enforcement-0001-of-0001.json.zip#results[2485]
FDA event record
· Exact recall-number query on openFDA
food · product 34 of 46
Garcinia Cambogia Extract, Capsules
F-2275-2014
Recall number F-2275-2014
Initiated July 03, 2014
Classification Class II
Status Terminated
Quantity 21,600 units
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
violations of the cGMP
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall GM Manufacturing is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.
Code information 10/26/12 > 10/29/12
Official fact provenance
Dataset openFDA Food Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 ccbd901395e7f97453ba67323214b452ee901a828cb9048da8cb62e875bf39dc
Raw source locator 0001-food-enforcement-0001-of-0001.json.zip#results[6364]
FDA event record
· Exact recall-number query on openFDA
food · product 35 of 46
Nano Papa
F-2276-2014
Recall number F-2276-2014
Initiated July 03, 2014
Classification Class II
Status Terminated
Quantity 60,840 units
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
violations of the cGMP
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall GM Manufacturing is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.
Code information 8/22/13 > 8/26/13 8/29/13 > 9/6/13 10/8/13 > 10/10/13
Official fact provenance
Dataset openFDA Food Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 ccbd901395e7f97453ba67323214b452ee901a828cb9048da8cb62e875bf39dc
Raw source locator 0001-food-enforcement-0001-of-0001.json.zip#results[4147]
FDA event record
· Exact recall-number query on openFDA
food · product 36 of 46
Kidney&Chi Plus, Bottles
F-2277-2014
Recall number F-2277-2014
Initiated July 03, 2014
Classification Class II
Status Terminated
Quantity 674 units
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
violations of the cGMP
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall GM Manufacturing is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.
Code information 724EXP08.2015 EXP12.2015
Official fact provenance
Dataset openFDA Food Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 ccbd901395e7f97453ba67323214b452ee901a828cb9048da8cb62e875bf39dc
Raw source locator 0001-food-enforcement-0001-of-0001.json.zip#results[4115]
FDA event record
· Exact recall-number query on openFDA
food · product 37 of 46
Detoxification Plus, Bottles
F-2278-2014
Recall number F-2278-2014
Initiated July 03, 2014
Classification Class II
Status Terminated
Quantity 338 units
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
violations of the cGMP
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall GM Manufacturing is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.
Code information 724EXP08.2015
Official fact provenance
Dataset openFDA Food Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 ccbd901395e7f97453ba67323214b452ee901a828cb9048da8cb62e875bf39dc
Raw source locator 0001-food-enforcement-0001-of-0001.json.zip#results[3989]
FDA event record
· Exact recall-number query on openFDA
food · product 38 of 46
Longetivity Plus, Bottles
F-2279-2014
Recall number F-2279-2014
Initiated July 03, 2014
Classification Class II
Status Terminated
Quantity 338 units
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
violations of the cGMP
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall GM Manufacturing is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.
Code information 724EXP08.2015
Official fact provenance
Dataset openFDA Food Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 ccbd901395e7f97453ba67323214b452ee901a828cb9048da8cb62e875bf39dc
Raw source locator 0001-food-enforcement-0001-of-0001.json.zip#results[5823]
FDA event record
· Exact recall-number query on openFDA
food · product 39 of 46
Stomach & Spleen Plus, Bottles
F-2280-2014
Recall number F-2280-2014
Initiated July 03, 2014
Classification Class II
Status Terminated
Quantity 338 units
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
violations of the cGMP
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall GM Manufacturing is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.
Code information 819EXP08.2015
Official fact provenance
Dataset openFDA Food Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 ccbd901395e7f97453ba67323214b452ee901a828cb9048da8cb62e875bf39dc
Raw source locator 0001-food-enforcement-0001-of-0001.json.zip#results[6358]
FDA event record
· Exact recall-number query on openFDA
food · product 40 of 46
Bone & Joint Plus, Bottles
F-2281-2014
Recall number F-2281-2014
Initiated July 03, 2014
Classification Class II
Status Terminated
Quantity 336 units
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
violations of the cGMP
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall GM Manufacturing is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.
Code information 819EXP08.2015
Official fact provenance
Dataset openFDA Food Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 ccbd901395e7f97453ba67323214b452ee901a828cb9048da8cb62e875bf39dc
Raw source locator 0001-food-enforcement-0001-of-0001.json.zip#results[4124]
FDA event record
· Exact recall-number query on openFDA
food · product 41 of 46
Circulation and Energy Formula, Bottles
F-2282-2014
Recall number F-2282-2014
Initiated July 03, 2014
Classification Class II
Status Terminated
Quantity 336 units
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
violations of the cGMP
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall GM Manufacturing is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.
Code information EXPFEB2015
Official fact provenance
Dataset openFDA Food Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 ccbd901395e7f97453ba67323214b452ee901a828cb9048da8cb62e875bf39dc
Raw source locator 0001-food-enforcement-0001-of-0001.json.zip#results[1593]
FDA event record
· Exact recall-number query on openFDA
food · product 42 of 46
Tendon & Muscle Plus, Bottles
F-2283-2014
Recall number F-2283-2014
Initiated July 03, 2014
Classification Class II
Status Terminated
Quantity 330 units
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
violations of the cGMP
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall GM Manufacturing is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.
Code information 509EXP05.2015
Official fact provenance
Dataset openFDA Food Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 ccbd901395e7f97453ba67323214b452ee901a828cb9048da8cb62e875bf39dc
Raw source locator 0001-food-enforcement-0001-of-0001.json.zip#results[6949]
FDA event record
· Exact recall-number query on openFDA
food · product 43 of 46
Vital Balance Formula, Bottles
F-2284-2014
Recall number F-2284-2014
Initiated July 03, 2014
Classification Class II
Status Terminated
Quantity 336 units
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
violations of the cGMP
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall GM Manufacturing is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.
Code information EXP12.2015
Official fact provenance
Dataset openFDA Food Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 ccbd901395e7f97453ba67323214b452ee901a828cb9048da8cb62e875bf39dc
Raw source locator 0001-food-enforcement-0001-of-0001.json.zip#results[4120]
FDA event record
· Exact recall-number query on openFDA
food · product 44 of 46
Via-Max Gold, Blister packs
F-2285-2014
Recall number F-2285-2014
Initiated July 03, 2014
Classification Class II
Status Terminated
Quantity 4,640 units
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
violations of the cGMP
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall GM Manufacturing is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.
Code information No Lot numbers
Official fact provenance
Dataset openFDA Food Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 ccbd901395e7f97453ba67323214b452ee901a828cb9048da8cb62e875bf39dc
Raw source locator 0001-food-enforcement-0001-of-0001.json.zip#results[5319]
FDA event record
· Exact recall-number query on openFDA
food · product 45 of 46
Albert, Capsules
F-2286-2014
Recall number F-2286-2014
Initiated July 03, 2014
Classification Class II
Status Terminated
Quantity 81,600 units
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
violations of the cGMP
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall GM Manufacturing is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.
Code information 3/6/12 > 3/8/12 6/1/12 > 6/4/12 8/3/12 > 8/3/12 9/6/12 > 9/6/12 9/21/12 > 9/28/12 10/16/12 > 10/16/12 11/8/12 > 11/8/12 11/29/12 > 11/29/12
Official fact provenance
Dataset openFDA Food Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 ccbd901395e7f97453ba67323214b452ee901a828cb9048da8cb62e875bf39dc
Raw source locator 0001-food-enforcement-0001-of-0001.json.zip#results[4132]
FDA event record
· Exact recall-number query on openFDA
food · product 46 of 46
CKLS, Capsules
F-2287-2014
Recall number F-2287-2014
Initiated July 03, 2014
Classification Class II
Status Terminated
Quantity 1,000,500 units
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
violations of the cGMP
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall GM Manufacturing is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.
Code information No Lot numbers
Official fact provenance
Dataset openFDA Food Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 ccbd901395e7f97453ba67323214b452ee901a828cb9048da8cb62e875bf39dc
Raw source locator 0001-food-enforcement-0001-of-0001.json.zip#results[2469]
FDA event record
· Exact recall-number query on openFDA
