Public Health Trace republishes official recall, outbreak, and surveillance data from CDC, FDA, USDA,
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Based on the official records currently available to Public Health Trace, 8 recalls naming Akron Pharma, Inc. are currently shown as ongoing. The other 3 records below are historical.
Public Health Trace has 11 recalls naming Akron Pharma, Inc. as the recalling firm, republished from official FDA and USDA sources.
Recall records - 11 total
Recalls by year
A bar chart of the number of recalls naming this company by year.
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.
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.
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.
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.
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.
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.
Some FDA recall records on this page come from FDA's Enforcement Report database.
Not every Enforcement Report record has a separate FDA.gov recall-announcement page.
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.
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