FDA Drug recall D-0135-2018
Bayer Chewable Low Dose Aspirin 81 mg Orange Flavored 36 tablets, Made in Spain, Distributed by: Bayer Healthcare LLC Morristown, NJ 07962…
- FDA Drug
- Class III
- terminated
- Published 2018-01-03
On 2018-01-03 the FDA classified a Class III recall of Bayer Chewable Low Dose Aspirin 81 mg Orange Flavored 36 tablets, Made in Spain, Distributed by: Bayer Healthcare LLC Morristown, NJ 07962… by Bayer Healthcare Pharmaceuticals, citing failed Stability Specifications.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-0135-2018 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2017-11-10 |
| Published | 2018-01-03 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Bayer Healthcare Pharmaceuticals |
| Distribution | n/a |
Product
Bayer Chewable Low Dose Aspirin 81 mg Orange Flavored 36 tablets, Made in Spain, Distributed by: Bayer Healthcare LLC Morristown, NJ 07962 NDC 0280-2160-36 UPC 3128431310577
Reason
Failed Stability Specifications
Identifiers
| upc | 3128431310577 |
|---|---|
| code_info | Lot # NAA3T0X; Exp. 07/18 |
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.
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Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0135-2018%22
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