Aidapak Recalls Glycopyrrolate Tablets Due to Potential Label Mixup
Aidapak Services, LLC is recalling 1,300 tablets of Glycopyrrolate 2 mg because they may have been mislabeled as other prescription drugs.
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 (label mixup) without reported illnesses or injuries, which aligns with the rubric for moderate severity involving minor labeling errors or low-risk contamination.
Plain-English summary
Aidapak Services, LLC is recalling 1,300 tablets of Glycopyrrolate 2 mg (NDC 00603318121) due to a potential label mixup. The recalled tablets may have been mislabeled as Paricalcitol 1 mcg capsules, Guaifenesin ER 600 mg tablets, or Lactobacillus tablets.
The repacked drugs were distributed in Arizona, California, Oregon, and Washington. The recall involves specific pedigree codes: W002650 (expiration 6/5/2014), W003252 (expiration 6/17/2014), and AD22865_4 (expiration 5/2/2014).
Consumers and healthcare providers should check their inventory for these specific NDC and pedigree codes. If the product is found, it should be returned to the distributor or disposed of according to local regulations. Patients should consult their healthcare provider if they have taken a medication that may have been mislabeled.
The recalled product
- Product
- GLYCOPYRROLATE, Tablet, 2 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00603318121.
- Manufacturer
- Aidapak Services, LLC
- Category
- Drug — Prescription Medication
- Hazard
- Affected units
- 1,300
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)
- GLYCOPYRROLATE
- Tablet
- 2 mg has the following codes: Pedigree: W002650
- 6/5/2014
- Pedigree: W003252
- 6/17/2014
- Pedigree: AD22865_4
- 5/2/2014.
Distribution
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.
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