Aidapak Recalls Citalopram Tablets Due to Potential Label Mixup
Aidapak Services, LLC is recalling 10 mg Citalopram tablets because they may be mislabeled as Oxybutynin Chloride or Coenzyme Q-10.
What this means for you
Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.
Our severity reasoning: The FDA classified this as a Class II recall. Per the rubric, FDA Class II recalls are assigned a severity score of 4 (Severe), particularly given the risk of administering the wrong medication.
Plain-English summary
Aidapak Services, LLC is recalling Citalopram Tablet, 10 mg, Rx only, distributed under NDC 57664050788. The recall is due to a labeling mixup where the product may be mislabeled as Oxybutynin Chloride, Tablet, 5 mg, or Coenzyme Q-10, Capsule, 30 mg.
The affected repacked drugs were distributed in Arizona, California, Oregon, and Washington. The recall involves 299 tablets with specific pedigree and expiration codes: Pedigree AD56921_1 (EXP 5/21/2014) and Pedigree W002844 (EXP 6/7/2014). The potential mislabels are associated with NDC 00603497521 (Pedigree AD52778_61, EXP 5/20/2014) and NDC 00904501546 (Pedigree W002814, EXP 6/7/2014).
Consumers and healthcare providers should check their inventory for these specific lot codes and stop using the product if it matches the description. The FDA has classified this as a Class II recall, indicating a situation that may cause temporary or medically reversible adverse health consequences.
The recalled product
- Product
- CITALOPRAM Tablet, 10 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 57664050788
- Manufacturer
- Aidapak Services, LLC
- Category
- Drug — Prescription Medication
- Affected units
- 299
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 (6)
- CITALOPRAM
- Tablet
- 10 mg has the following codes Pedigree: AD56921_1
- EXP: 5/21/2014
- Pedigree: W002844
- EXP: 6/7/2014.
Distribution
Part of a larger recall action
This product is one of 273 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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