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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 79936

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

Open FDA event record

Event summary

Timeline bucket
April 23, 2018
Product types
Drug
Classifications
Class III
Statuses
Terminated
Recalling firm wording
Mckesson Packaging Services

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

3 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 3

Diltiazem HCl Extended-Release Capsules, USP 120 mg, 100-count bottles, Rx only, Mfg. By: Par Pharmaceutical One Ram Ridge Rd Chestnut Ridge, NY 10977. NDC: 63739-014-10

D-0714-2018
Recall number
D-0714-2018
Initiated
April 23, 2018
Classification
Class III
Status
Terminated
Quantity
4266 cartons

App-derived interpretation

Potency or specification failure reason.potency_specification_failure · v1.0.0
Failed Dissolution Specifications

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Failed Dissolution Specifications. High dissolution results were obtained during stability testing.

Code information

Lot #: 0115086, Exp. 12/2018

Distribution pattern

Nationwide with the US

drug · product 2 of 3

Diltiazem CD (Diltiazem Hydrochloride Extended-Release Capsules, USP) 180 mg, 100-count bottles, Rx Only Mfg. By: Actavis 60 Columbia Rd., Bldg. B Morristown, NJ 07960. NDC 63739-284-10

D-0715-2018
Recall number
D-0715-2018
Initiated
April 23, 2018
Classification
Class III
Status
Terminated
Quantity
7656 cartons

App-derived interpretation

Potency or specification failure reason.potency_specification_failure · v1.0.0
Failed Dissolution Specifications

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Failed Dissolution Specifications. High dissolution results were obtained during stability testing.

Code information

Lot #: 0114214, Exp. 09/2018

Distribution pattern

Nationwide with the US

drug · product 3 of 3

Diltiazem HCl Extended-Release Capsules, USP 240 mg, 100-count bottles, Rx Only, Mfg. By: Par Pharmaceutical One Ram Ridge Rd Chestnut Ridge, NY 10977. NDC: 63739-016-10

D-0716-2018
Recall number
D-0716-2018
Initiated
April 23, 2018
Classification
Class III
Status
Terminated
Quantity
2966 cartons

App-derived interpretation

Potency or specification failure reason.potency_specification_failure · v1.0.0
Failed Dissolution Specifications

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Failed Dissolution Specifications. High dissolution results were obtained during stability testing.

Code information

Lot #: 0115087, Exp. 12/2018

Distribution pattern

Nationwide with the US