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Akron Pharma, Inc.

Recalls

Recalls by year

A bar chart of the number of recalls naming this company by year.

Recalls by year
YearRecalls
20222
20231
20241
20257
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FDA Recall Ongoing Historical recordClass III

Diphenhydramine HCl 50 mg, 1000 capsules per bottle, Akron Pharma, Manufactured for: Akron Pharma, Inc. 373 Route US 46, Building E, Suite 117, Fairfield, NJ 07004, NDC 71399-8026-02.

by Akron Pharma, Inc.

Reason
Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
Published
January 22, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass III

Diphenhydramine HCl 25 mg, 1000 Capsules per bottle, Akron Pharma, Manufactured for: Akron Pharma, Inc., 373 RT US 46 W Building E., Suite 117, Fairfield, NJ 07004, NDC 71399-8028-2.

by Akron Pharma, Inc.

Reason
Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
Published
January 22, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass III

Diphenhydramine HCl 25 mg, 100 capsules per bottle, Akron Pharma, Manufactured for: Akron Pharma, Inc., 373 RT US 46 W Building E, Suite 117, Fairfield, NJ 07004, NDC 71399-8028-1.

by Akron Pharma, Inc.

Reason
Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
Published
January 22, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass III

Acetaminophen Extra Strength 500 mg, 1000 Tablets per bottle, Akron Pharma, Manufactured for: Akron Pharma Inc., 373 US RT 46 W Building E, Suite 117, Fairfield, NJ 07034, NDC 71399-8022-02

by Akron Pharma, Inc.

Reason
Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
Published
January 22, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass III

Acetaminophen, 325 mg Tablets, 100 Tablets per bottle, Akron Pharma, Manufactured for: Akron Pharma Inc., Fairfield, NJ 07034, NDC 71399-8014-01.

by Akron Pharma, Inc.

Reason
Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
Published
January 22, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass III

Acetaminophen Regular Strength, 325 mg, 100 Tablets per bottle, Akron Pharma, Inc., 373 RT US 46 W Building E, Suite 117, Fairfield, NJ 07004, NDC 71399-8024-01 .

by Akron Pharma, Inc.

Reason
Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
Published
January 22, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass III

Acetaminophen Extra Strength 500 mg, 100 Tablets per bottle, Akron Pharma, Inc., 373 RT US 46 W Building E, Suite 117, Fairfield, NJ 07004, NDC 71399-8022-01.

by Akron Pharma, Inc.

Reason
Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
Published
January 22, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

OneLAX Docusate Sodium Liquid (docusate sodium 50 mg/5 mL) Stool Softener Laxative, 16 FL OZ (473 mL) bottle, Akron Pharma, Manufactured for: Akron Pharma, Inc., Fairfield, NJ 07004, NDC 71399-0039-06.

by Akron Pharma, Inc.

Reason
CGMP Deviations
Published
October 30, 2024
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

DIBUCAINE 1% HEMORRHOIDAL OINTMENT, 1 oz. (28 gm), Manufactured for: Akron Pharma Inc. Fairfield NJ 07004, NDC 71399-2829-1

by Akron Pharma, Inc.

Reason
Labeling: Incorrect or Missing Lot and/or Exp Date
Published
March 15, 2023
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

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

by Akron Pharma, Inc.

Reason
Failed Tablet/Capsule Specifications: Imprint "AP 325" is missing from the tablet.
Published
August 24, 2022
Distribution
Product was distributed to 6 distributor…

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FDA Recall Terminated Historical recordClass III

Acetaminophen 325 mg tablets, packaged in a) 100-count bottle (NDC 71399-8024-01); b) 1000-count bottle (NDC 71399-8024-02), Akorn Pharma Manufactured for: Akorn Pharma, Inc., Fairfield, NJ

by Akron Pharma, Inc.

Reason
Failed Tablet/Capsule Specifications: Imprint "AP 325" is missing from the tablet.
Published
August 24, 2022
Distribution
Product was distributed to 6 distributor…

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Showing 1–11 of 11 results

This page lists recalls that name Akron Pharma, Inc. as the recalling firm in the official source notice. It is not a safety rating, ranking, or statement that the company acted negligently. Read the full medical disclaimer.