RecallRadar

FDA Drug recall D-1820-2019

Aspirin and Extended-release Dipyridamole Capsules, 25 mg/200 mg, 20 capsules per carton (5 blister cards x 4 unit doses), Rx Only, Distrib…

On 2019-08-21 the FDA classified a Class II recall of Aspirin and Extended-release Dipyridamole Capsules, 25 mg/200 mg, 20 capsules per carton (5 blister cards x 4 unit doses), Rx Only, Distrib… by American Health Packaging, citing failed Impurities/Degradation Specifications; out of specification result for an unknown impurity in stability samples.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-1820-2019
ClassificationClass II
Statusterminated
Initiated2019-03-01
Published2019-08-21
Last updated2026-09-13 11:52 UTC
CompanyAmerican Health Packaging
DistributionUS

Product

Aspirin and Extended-release Dipyridamole Capsules, 25 mg/200 mg, 20 capsules per carton (5 blister cards x 4 unit doses), Rx Only, Distributed by: American Health Packaging, Columbus, Ohio 43217. NDC Carton: 60687-305-32; NDC Blister Pack: 60687-305-33

Reason

Failed Impurities/Degradation Specifications; out of specification result for an unknown impurity in stability samples.

Identifiers

code_info
Lot, expiry: Lot 174262, exp. 03/31/2019; Lot 176469, exp. 06/30/2019; Lot 177897, exp. 08/31/2019; Lots 178318 and 1…Lot, expiry: Lot 174262, exp. 03/31/2019; Lot 176469, exp. 06/30/2019; Lot 177897, exp. 08/31/2019; Lots 178318 and 178436, exp. 09/30/2019; Lot 179547 and 179656, exp. 11/30/2019

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1820-2019%22

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