Recall events
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Event 66843
Event summary
Timeline bucket October 25, 2013
Product types Food
Classifications Class II
Statuses Terminated
Recalling firm wording Health Wright Products 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
9 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 9
Digestive, Enzyme Supplement, packaged 90 capsules per bottle, 135 capsules per bottle, or 270 capsules per bottle. They are sold under brand Enzyme Research Products or Empower Life.
F-1453-2014
Recall number F-1453-2014
Initiated October 25, 2013
Classification Class II
Status Terminated
Quantity 1199 bottles of 90 ct; 2081 bottles of 135 ct; 9799 bottles of 270 ct;
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Dietary supplement products are recalled because they were made from ingredient that was contaminated with Chloramphenicol.
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Dietary supplement products are recalled because they were made from ingredient that was contaminated with Chloramphenicol.
Code information Digestive (90 count): LOT #1206801, EXP 03/15 (means March 2015); Digestive (135 count): LOT # 1108103, EXP 03/14 (means March 2014); LOT# 1234006, EXP 12/15 (means December 2015) for Empower Life Nutrition brand. Digestive (270 count): LOT# 1127002, EXP 09/14 (means September 2014); LOT# 1120606, EXP 07/14 (means July 2014); LOT# 1113201, EXP 05/14 (means May 2014); LOT# 1029104, EXP 10/13 (means October 2013); LOT# 1215601, EXP 06/15 (means June 2015); LOT# 1234006, EXP 12/15 (means December 2015).
Distribution pattern Distributed to California, Florida, Oregon, Utah, and Mexico
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[6104]
FDA event record
· Exact recall-number query on openFDA
food · product 2 of 9
B-Complex with Enzymes, Vitamin/Enzyme Supplement. Packaged 60 vegetable capsules per bottle. They are sold under brand Enzyme Research Products.
F-1454-2014
Recall number F-1454-2014
Initiated October 25, 2013
Classification Class II
Status Terminated
Quantity 991 bottles
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Dietary supplement products are recalled because they were made from ingredient that was contaminated with Chloramphenicol.
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Dietary supplement products are recalled because they were made from ingredient that was contaminated with Chloramphenicol.
Code information LOT# 1224405, EXP 08/15 (means August 2015)
Distribution pattern Distributed to California, Florida, Oregon, Utah, and Mexico
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[6862]
FDA event record
· Exact recall-number query on openFDA
food · product 3 of 9
B-Complex Plus. They are sold under brand Enzyme Research Products
F-1455-2014
Recall number F-1455-2014
Initiated October 25, 2013
Classification Class II
Status Terminated
Quantity 1033 bottles
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Dietary supplement products are recalled because they were made from ingredient that was contaminated with Chloramphenicol.
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Dietary supplement products are recalled because they were made from ingredient that was contaminated with Chloramphenicol.
Code information LOT# 1108001, EXP 03/14 (means March 2014)
Distribution pattern Distributed to California, Florida, Oregon, Utah, and Mexico
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[4429]
FDA event record
· Exact recall-number query on openFDA
food · product 4 of 9
Glucosamine, Chondroitin, MSM Plus, dietary supplement, 60 capsules per bottle. They are sold under brand Enzyme Research Products or Empower Life Vital Joints brand.
F-1456-2014
Recall number F-1456-2014
Initiated October 25, 2013
Classification Class II
Status Terminated
Quantity 3127 bottles
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Dietary supplement products are recalled because they were made from ingredient that was contaminated with Chloramphenicol.
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Dietary supplement products are recalled because they were made from ingredient that was contaminated with Chloramphenicol.
Code information LOT# 1125804, EXP 09/14 (means September 2014); LOT# 1214301, EXP 05/15 (means May 2015); LOT# 1308601; EXP 03/16 (means March 2016);
Distribution pattern Distributed to California, Florida, Oregon, Utah, and Mexico
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[6066]
FDA event record
· Exact recall-number query on openFDA
food · product 5 of 9
Zinc Plus, Mineral/Enzyme supplement, 90 vegetable capsules per bottle. They are sold under brand Enzyme Research Products.
F-1457-2014
Recall number F-1457-2014
Initiated October 25, 2013
Classification Class II
Status Terminated
Quantity 1914 bottles
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Dietary supplement products are recalled because they were made from ingredient that was contaminated with Chloramphenicol.
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Dietary supplement products are recalled because they were made from ingredient that was contaminated with Chloramphenicol.
Code information LOT# 1228603, EXP 10/15 (means October 2015); LOT# 1134004, EXP 12/14 (means December 2014);
Distribution pattern Distributed to California, Florida, Oregon, Utah, and Mexico
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[6115]
FDA event record
· Exact recall-number query on openFDA
food · product 6 of 9
Digestaze, dietary supplement, 90 vegetable capsules per bottle. They are sold under brand DESBIO
F-1458-2014
Recall number F-1458-2014
Initiated October 25, 2013
Classification Class II
Status Terminated
Quantity 1137 bottles
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Dietary supplement products are recalled because they were made from ingredient that was contaminated with Chloramphenicol.
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Dietary supplement products are recalled because they were made from ingredient that was contaminated with Chloramphenicol.
Code information LOT# 1215904, EXP 06/14 (means June 2014).
Distribution pattern Distributed to California, Florida, Oregon, Utah, and Mexico
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[6083]
FDA event record
· Exact recall-number query on openFDA
food · product 7 of 9
Enzyme Formula, dietary supplement, 100 capsules or 250 capsules per bottles, sold unlabeled to Rich Distributing.
F-1459-2014
Recall number F-1459-2014
Initiated October 25, 2013
Classification Class II
Status Terminated
Quantity 200 bottles (100 ct); 367 bottles (250 ct)
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Dietary supplement products are recalled because they were made from ingredient that was contaminated with Chloramphenicol.
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Dietary supplement products are recalled because they were made from ingredient that was contaminated with Chloramphenicol.
Code information LOT# 1319603, EXP 07/15
Distribution pattern Distributed to California, Florida, Oregon, Utah, and Mexico
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[6072]
FDA event record
· Exact recall-number query on openFDA
food · product 8 of 9
XymoZyme, dietary supplement, packaged 60 capsules per bottte, 120 capsules per bottle, sold under brand ZYMOGEN.
F-1460-2014
Recall number F-1460-2014
Initiated October 25, 2013
Classification Class II
Status Terminated
Quantity 7890 bottles
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Dietary supplement products are recalled because they were made from ingredient that was contaminated with Chloramphenicol.
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Dietary supplement products are recalled because they were made from ingredient that was contaminated with Chloramphenicol.
Code information 60 count bottle: LOT# 1207301D, EXP 03/14 (means March 2014); LOT# 1221501D, EXP 08/14 (means August 2014); LOT# 1229205D, EXP 10/14 (means October 2014); 120 count bottle: LOT# 1207301H; EXP 03/14 (means March 2014); LOT# 1221501H, EXP 08/14 (means August 2014); LOT# 1229205H, EXP 10/14 (means October 2014);
Distribution pattern Distributed to California, Florida, Oregon, Utah, and Mexico
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[6079]
FDA event record
· Exact recall-number query on openFDA
food · product 9 of 9
Digest Ultra, dietary supplement, packaged 56 capsules per bottle or distributed in bulk, sold under brand YOR. Product distributed OUTSIDE the US has Spanish label.
F-1461-2014
Recall number F-1461-2014
Initiated October 25, 2013
Classification Class II
Status Terminated
Quantity 82,906 bottles and 1,552,319 capsules (bulk) in US and 62766 bottles OUTSIDE the US
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Dietary supplement products are recalled because they were made from ingredient that was contaminated with Chloramphenicol.
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Dietary supplement products are recalled because they were made from ingredient that was contaminated with Chloramphenicol.
Code information LOT Numbers: 1207408; MFG -03/12; 1217703; MFG -06/12; 10190112; MFG -01/12; 10190112; MFG -01/12; 10190312; MFG-03/12; 10190313; MFG -03/13; 10191112; MFG -11/12; 20190313; EXP- 2/2015; 20190612; EXP- 06/14; 20191012; EXP -10/14; 1019A0811; EXP- 08/13 ;
Distribution pattern Distributed to California, Florida, Oregon, Utah, and Mexico
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[2816]
FDA event record
· Exact recall-number query on openFDA