Aspirin Chewable tablet 81 mg Recall: CGMP Deviations
Aspirin Chewable tablet 81 mg, 1 tablet in blister card-foils, 100-count unit dose box, www.safecorhealth.com, NDC 48433-129-01
What is the FDA recall status?
The FDA record lists this recall as ongoing. FDA enforcement data is not a live recall-lifecycle tracker. Follow the official instructions and check the agency notice or firm for current guidance.
Why was Aspirin Chewable tablet 81 mg recalled?
cGMP Deviations: Observations were made that some blister card-foils were separating from the blister cavity.
What should I do if I have this product?
Follow the firm and FDA instructions for the affected product. Contact the recalling firm for current guidance.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare your product with the product description and available lot, UPC or model codes below from the official FDA record to check whether it is covered by this recall. If an identifier is missing or unclear, check the complete official notice or contact the firm; an incomplete match here does not establish that your product is unaffected.
Full product description
Aspirin Chewable tablet 81 mg, 1 tablet in blister card-foils, 100-count unit dose box, www.safecorhealth.com, NDC 48433-129-01
Which lot codes, UPCs or models are affected?
Lot# 24A0061, exp. date 05/23/2026
- Agency record number
- D-0058-2025
- Product
- Aspirin Chewable tablet 81 mg, 1 tablet in blister card-foils, 100-count unit dose box, www.safecorhealth.com, NDC 48433-129-01
- Recalling firm
- Safecor Health, LLC
- Quantity
- 1470 boxes
- Distribution
- USA nationwide.
- Recall started
- November 11, 2024
- Report date
- November 27, 2024
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (drug)