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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 73152

4 recalled-product records grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
January 27, 2016
Product types
Drug
Classifications
Class III
Statuses
Terminated
Recalling firm wording
Golden State Medical Supply Inc.

Dossier provenance

Source snapshots represented here

  • openFDA Drug 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

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.

drug · product 1 of 4

Atorvastatin Calcium 10 mg, 10 tablets per blister,100-count package, Rx Only Manufactured by Apotex Inc. Toronto, Ontario, Canada, Packaged by GSMS Inc., Camarillo, CA 93010, NDC # 60429-323-77

D-0767-2016
Recall number
D-0767-2016
Initiated
January 27, 2016
Classification
Class III
Status
Terminated
Quantity
222 100-count packages (22,000 tablets)

App-derived interpretation

Potency or specification failure reason.potency_specification_failure · v1.0.0
Failed Impurities/Degradation Specifications

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Failed Impurities/Degradation Specifications

Code information

Lot #GS005602; Exp. 10/15 Lot #GS008855; Exp. 09/17 Lot #GS009074; Exp. 08/17 Lot #GS009393; Exp. 08/17 Lot #GS009760; Exp. 10/17 Lot #GS010599; Exp. 11/17

Distribution pattern

Nationwide

drug · product 2 of 4

Atorvastatin Calcium 20 mg, 10 tablets per blister,100-count package, Rx Only Manufactured by Apotex Inc. Toronto, Ontario, Canada, Packaged by GSMS Inc., Camarillo, CA 93010, NDC # 60429-324-77

D-0768-2016
Recall number
D-0768-2016
Initiated
January 27, 2016
Classification
Class III
Status
Terminated
Quantity
74 100-count packages (7,400 tablets)

App-derived interpretation

Potency or specification failure reason.potency_specification_failure · v1.0.0
Failed Impurities/Degradation Specifications

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Failed Impurities/Degradation Specifications

Code information

Lot #GS008856; Exp. 09/17 Lot #GS010268; Exp. 09/17 Lot #GS010600; Exp. 11/17

Distribution pattern

Nationwide

drug · product 3 of 4

Atorvastatin Calcium 40 mg, 10 tablets per blister,100-count package, Rx Only Manufactured by Apotex Inc. Toronto, Ontario, Canada, Packaged by GSMS Inc., Camarillo, CA 93010, NDC # 60429-325-77

D-0769-2016
Recall number
D-0769-2016
Initiated
January 27, 2016
Classification
Class III
Status
Terminated
Quantity
172 100-count packages (17,200 tablets)

App-derived interpretation

Potency or specification failure reason.potency_specification_failure · v1.0.0
Failed Impurities/Degradation Specifications

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Failed Impurities/Degradation Specifications

Code information

Lot #GS009075; Exp. 09/17 Lot #GS009763; Exp. 09/17 Lot #GS010178; Exp. 10/17

Distribution pattern

Nationwide

drug · product 4 of 4

Atorvastatin Calcium 80 mg, 10 tablets per blister,100-count package, Rx Only Manufactured by Apotex Inc. Toronto, Ontario, Canada, Packaged by GSMS Inc., Camarillo, CA 93010, NDC # 60429-326-77

D-0770-2016
Recall number
D-0770-2016
Initiated
January 27, 2016
Classification
Class III
Status
Terminated
Quantity
168 100-count packages (16,800 tablets)

App-derived interpretation

Potency or specification failure reason.potency_specification_failure · v1.0.0
Failed Impurities/Degradation Specifications

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Failed Impurities/Degradation Specifications

Code information

Lot #GS005603; Exp. 10/15 Lot #GS006691; Exp. 08/17 Lot #GS009073; Exp. 08/17 Lot #GS009395; Exp. 08/17 Lot #GS009764; Exp. 10/17

Distribution pattern

Nationwide