Severity
Low
LowClass IIITerminated
FDA Drug recall · Reported August 24, 2022
Acetaminophen 500 mg tablet, Extra Strength, packaged in a) 100-count bottle (NDC 71399-8022-01), b) 1000-count bottle (NDC 71399-8022-02), Akorn Pharma Manufactured for: Akorn Pharma, Inc., Fairfield, NJ
Failed Tablet/Capsule Specifications: Imprint "AP 325" is missing from the tablet.
Compiled from official public sources by the editorial team.
Verify with FDA Drug →
Akron Pharma, Inc. recalled Acetaminophen 500 mg tablet, Extra Strength, packaged in a) 100-count bottle (NDC 71399-8… - a low-severity action.
Acetaminophen 500 mg tablet, Extra Strength, packaged in a) 100-count bottle (NDC 71399-8… was recalled by Akron Pharma, Inc. in August 24, 2022. Reason: Failed Tablet/Capsule Specifications: Imprint "AP 325" is missing from the tablet.. Check the official notice for the remedy. Verify recall #D-1353-2022 with the FDA Drug before acting.
The recall
Akron Pharma, Inc. issued this low-severity FDA Drug recall-Failed Tablet/Capsule Specifications: Imprint "AP 325" is missing from the tablet..
- Low
- severity level
- Class III
- classification
- August 24, 2022
- reported
Sourced from official FDA Drug enforcement records. Verify recall #D-1353-2022 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Drug action (record #D-1353-2022) was formally reported on August 24, 2022, with the manufacturer initiating the action on August 4, 2022. It is classified under Low severity (Class III), with a current status of Terminated. Akron Pharma, Inc. is listed as the recalling firm, operating out of Fairfield, NJ. Federal records list the affected scope as 30,325 bottles.
The documented reason for this recall is: Failed Tablet/Capsule Specifications: Imprint "AP 325" is missing from the tablet. Distribution data in the federal record shows the product reached: Product was distributed to 6 distributors/wholesalers who may have further distributed the product.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 5 from FDA Drug - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Drugs & Medications recalls over time
Where this recall sits in its category - 14,287 drugs & medications recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified low severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
30,325 bottles
Related Recalls
6
5 from same agency
Product description
Acetaminophen 500 mg tablet, Extra Strength, packaged in a) 100-count bottle (NDC 71399-8022-01), b) 1000-count bottle (NDC 71399-8022-02), Akorn Pharma Manufactured for: Akorn Pharma, Inc., Fairfield, NJ
Reason for recall
Failed Tablet/Capsule Specifications: Imprint "AP 325" is missing from the tablet.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Low (Class III) |
| Status | Terminated |
| Recall number | D-1353-2022 |
| Date reported | August 24, 2022 |
| Date initiated | August 4, 2022 |
| Recalling firm | Akron Pharma, Inc. |
| Firm location | Fairfield, NJ |
| Affected scope | 30,325 bottles |
| Distribution | Product was distributed to 6 distributors/wholesalers who may have further distributed the product. |
Profile values are sourced directly from the official FDA Drug enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (D-1353-2022) and product description against the item you own. Search the archive
- Confirm the current status with FDA Drug before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Drug record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
Acetaminophen 500 mg tablet, Extra Strength, packaged in a) 100-count bottle (NDC 71399-8022-01), b) 1000-count bottle (NDC 71399-8022-02), Akorn Pharma Manufactured for: Akorn Pharma, Inc., Fairfield, NJ. Recalled by Akron Pharma, Inc.. Units affected: 30,325 bottles.
Why was this product recalled? ▼
Failed Tablet/Capsule Specifications: Imprint "AP 325" is missing from the tablet.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on August 24, 2022. Severity: Low. Recall number: D-1353-2022.
Where was the recalled product distributed? ▼
Distribution: Product was distributed to 6 distributors/wholesalers who may have further distributed the product..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (D-1353-2022) against your product. Visit the official FDA Drug website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
Should I stop using a recalled medication or medical device? ▼
Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.
Nearby Recalls in This Category
Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
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Compare this recall with PRED MILD, prednisolone acetate ophthalmic suspension, USP,… →
Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Drug, reported August 24, 2022. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.