Recall events
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Event 75121
Event summary
Timeline bucket August 26, 2016
Product types Device
Classifications Class II
Statuses Terminated
Recalling firm wording The Anspach Effort, Inc.
Dossier provenance
Source snapshots represented here
openFDA Device 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.
openFDA Device Recall
event_date_initiated coverage
June 01, 1997–June 30, 2026
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
Complete imported group
Every recalled product in this event
4 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.
device · product 1 of 4
G1 Dissection Tool - 7mm FBALL L; For cutting and shaping bone including spine and cranium.
Z-2837-2016
Recall number Z-2837-2016
Initiated August 26, 2016
Classification Class II
Status Terminated
Quantity 177
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Product Code L- 7B-G1 was inadvertently released off of hold status and the affected products were distributed.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Device Design
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2837-2016
Source locator 0001-device-recall-0001-of-0001.json.zip#results[51231]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
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Reason for recall Product Code L- 7B-G1 was inadvertently released off of hold status and the affected products were distributed.
Code information Material L-7B-G1 Batch K043113667
Distribution pattern AZ, DC, CA, MD, MI, and OR Switzerland
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[10829]
FDA event record
· Exact recall-number query on openFDA
device · product 2 of 4
G1 Dissection Tool - 3mm CRS DBALL, 2mm SHAFT EXP, M; For cutting and shaping bone including spine and cranium.
Z-2838-2016
Recall number Z-2838-2016
Initiated August 26, 2016
Classification Class II
Status Terminated
Quantity 88
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
The firm discovered on March 4, 2016 that several product codes were inadvertently left off of Hold 1503.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Device Design
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2838-2016
Source locator 0001-device-recall-0001-of-0001.json.zip#results[39124]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
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Inspect official wording and provenance
Reason for recall The firm discovered on March 4, 2016 that several product codes were inadvertently left off of Hold 1503.
Code information Material M-3DC-2-G1 Batch J313108568 & J316017637
Distribution pattern AZ, DC, CA, MD, MI, and OR Switzerland
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[11671]
FDA event record
· Exact recall-number query on openFDA
device · product 3 of 4
G1 Dissection Tool - 3mm FLUTED BALL; For cutting and shaping bone including spine and cranium.
Z-2839-2016
Recall number Z-2839-2016
Initiated August 26, 2016
Classification Class II
Status Terminated
Quantity 63
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
The firm discovered on March 4, 2016 that several product codes were inadvertently left off of Hold 1503.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Device Design
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2839-2016
Source locator 0001-device-recall-0001-of-0001.json.zip#results[20607]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall The firm discovered on March 4, 2016 that several product codes were inadvertently left off of Hold 1503.
Code information Material M-3SB-2-G1 Batch J316017640
Distribution pattern AZ, DC, CA, MD, MI, and OR Switzerland
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[10208]
FDA event record
· Exact recall-number query on openFDA
device · product 4 of 4
G1 Dissection Tool - 6MM CRS DBALL, 2mm Shaft EXP, M; For cutting and shaping bone including spine and cranium.
Z-2840-2016
Recall number Z-2840-2016
Initiated August 26, 2016
Classification Class II
Status Terminated
Quantity 69
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
The firm discovered on March 4, 2016 that several product codes were inadvertently left off of Hold 1503.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Device Design
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2840-2016
Source locator 0001-device-recall-0001-of-0001.json.zip#results[39127]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall The firm discovered on March 4, 2016 that several product codes were inadvertently left off of Hold 1503.
Code information Material M-6DC-2-G1 Batch J313108573 and J 316017642
Distribution pattern AZ, DC, CA, MD, MI, and OR Switzerland
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[8323]
FDA event record
· Exact recall-number query on openFDA
