The Recall Desk
ModerateFDA (Drugs)·D-980-2014·Announced 2014-01-29

Aidapak Recalls Aspirin/ER Dipyridamole Capsules Due to Labeling Error

Aidapak Services, LLC is recalling Aspirin/ER Dipyridamole capsules because they may have been mislabeled as other medications.

What this means for you

Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.

Our severity reasoning: The recall is classified as FDA Class II and involves a labeling error (mislabeling) without reported injuries or illnesses, fitting the criteria for a moderate severity score.

Plain-English summary

Aidapak Services, LLC is recalling Aspirin/ER Dipyridamole, Capsule, 25 mg/200 mg, NDC 00597000160. The recall is due to a labeling error where the product may have been mislabeled as Thiamine HCL, Levothyroxine Sodium, or Zinc Sulfate.

The affected repacked drugs were distributed in Arizona, California, Oregon, and Washington. Specific pedigree codes and expiration dates are listed in the recall notice for identification.

Consumers should check their medication for the specific NDC and pedigree codes listed in the official recall notice. If the medication matches the recalled product, they should stop using it and contact their pharmacist or healthcare provider for instructions on disposal or replacement.

The recalled product

Product
ASPIRIN/ER DIPYRIDAMOLE, Capsule, 25 mg/200 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00597000160.
Affected units
300

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (8)

  • ASPIRIN/ER DIPYRIDAMOLE
  • Capsule
  • 25 mg/200 mg has the following codes: Pedigree: AD70639_4
  • EXP: 7/28/2013
  • Pedigree: W003468
  • EXP: 8/19/2013
  • Pedigree: W003644
  • EXP: 8/24/2013.

Distribution

Distributed in 4 states:

Part of a larger recall action

This product is one of 265 recalled by Aidapak Services, LLC under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 265 products in this recall →

Same manufacturer · Aidapak Services, LLC

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