Aspirin 81 mg chewable tablets recalled due to packaging defect
Safecor Health, LLC is recalling 1,470 boxes of Aspirin 81 mg chewable tablets nationwide due to a manufacturing defect where blister card-foils are separating from the blister cavity.
The agency’s classification
FDA (Drugs): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 2/5 (Moderate).
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: FDA Class II recall for a manufacturing defect with no reported illnesses or injuries. The hazard is a packaging integrity issue (blister separation) with no confirmed harm, consistent with a precautionary manufacturing recall scoring Moderate (2).
Plain-English summary
Safecor Health, LLC initiated a recall of 1,470 boxes of Aspirin 81 mg chewable tablets (NDC 48433-129-01) distributed nationwide. The affected product is lot number 24A0061 with an expiration date of May 23, 2026.
The recall was prompted by observations of cGMP deviations during manufacturing, specifically that some blister card-foils were separating from the blister cavity. This defect was identified through quality control processes.
Consumers who purchased this product should contact Safecor Health, LLC (www.safecorhealth.com) for information on the recall. Pharmacists and healthcare providers should identify and quarantine affected inventory.
The recalled product
- Product
- ASPIRIN (ASPIRIN 81 MG)
- Brand
- ASPIRIN
- Manufacturer
- Safecor Health, LLC
- Affected units
- 1,470
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 (2)
- Lot# 24A0061
- exp. date 05/23/2026
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 5 recalled by Safecor Health, 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.
See all 5 products in this recall →Related recalls
Same brand · ASPIRIN
- HighLow-dose aspirin recall due to improper storage temperature conditions
FDA (Drugs) · 2024-01-03
Same manufacturer · Safecor Health, LLC
See all →- ModerateSafecor Health Recalls Fluphenazine HCl Elixir Due to Stability Failures
FDA (Drugs) · 2026-09-23
- ModerateSafecor Health Recalls Fluphenazine HCl Elixir Due to Stability Failures
FDA (Drugs) · 2026-09-23
- ModerateSafecor Health Recalls Fluphenazine HCl Elixir Due to Stability Failures
FDA (Drugs) · 2026-09-23
- ModerateSafecor Health Recalls Fluphenazine HCl Elixir Due to Stability Failures
FDA (Drugs) · 2026-09-23
- ModerateSafecor Health Recalls Fluphenazine HCl Elixir Due to Stability Failures
FDA (Drugs) · 2026-09-23
Same hazard · blister separation
See all →- ModerateVitamin D3 Dietary Supplement Recalled for Packaging Defect
FDA (Drugs) · 2024-11-27
- ModerateVitamin B1 Supplement Recalled for Blister Packaging Defect
FDA (Drugs) · 2024-11-27
Similar recalls
- SevereMcKesson Recalls Aspirin Chewable Tablets Due to Foreign Material
FDA (Drugs) · 2017-03-15
- ModerateAllegiant Health Recalls HealthA2Z Chewable Aspirin Due to Rubber Particles
FDA (Drugs) · 2017-03-08
- ModerateBayer Chewable Low Dose Aspirin Recalled for Failed Stability Specifications
FDA (Drugs) · 2018-01-03
- SevereAmerican Health Packaging Recalls Aspirin and Dipyridamole Capsules
FDA (Drugs) · 2019-08-21
- ModerateAidapak Recalls Aspirin Chew Tablets Due to Potential Label Mixup
FDA (Drugs) · 2014-01-29
- LowSKY Aspirin Chewable Tablets Recalled for Incorrect Outer Carton Labeling
FDA (Drugs) · 2016-05-04