FDA Recalls Vitamin B Complex Tablets Due to Potential Label Mixup
Aidapak Services, LLC is recalling Vitamin B Complex tablets that may have been mislabeled as Cinacalcet HCl. The repacked drugs were distributed in four western states.
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 recall is classified as FDA Class II. Per the rubric, FDA Class II recalls with potential for significant injury or adverse health consequences (such as taking the wrong medication) are classified as Severe (Score 4).
Plain-English summary
Aidapak Services, LLC is recalling 100-tablet bottles of Vitamin B Complex with C (NDC 00536730001) because the product may have been mislabeled as Cinacalcet HCl 30 mg (NDC 55513007330). The recall involves repacked drugs with pedigree AD52993_7 and an expiration date of May 20, 2014.
The affected repacked drugs were distributed in Arizona, California, Oregon, and Washington. This labeling error could result in patients receiving the wrong medication, which poses a risk of harm if the incorrect drug is taken.
Consumers who have this product should stop using it and contact their pharmacist or healthcare provider for guidance. The recall is classified as Class II by the FDA, indicating a reasonable probability of temporary or medically reversible adverse health consequences.
The recalled product
- Product
- VITAMIN B COMPLEX W/C, Tablet, 0 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00536730001.
- Manufacturer
- Aidapak Services, LLC
- Category
- Drug — Over-The-Counter
- Affected units
- 100
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 (4)
- VITAMIN B COMPLEX W/C
- Tablet
- 0 mg has the following codes: Pedigree: AD52993_7
- EXP: 5/20/2014.
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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