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Akron Pharma, Inc.

Akron Pharma, Inc. Recalls

All product recalls associated with Akron Pharma, Inc..

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

127

Most Recent

Jan 2026

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 1481–1500 of 25000 recalls

Diphenhydramine HCl 50mg (Akron Pharma) – Incorrect Tablet Imprint (2024)

Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.

Class IIILow

FDADec 12, 2024Nationwide• Akron Pharma, Inc.

Diphenhydramine HCl 25mg 100ct (Akron Pharma) – Incorrect Tablet Imprint (2024)

Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.

Class IIILow

FDADec 12, 2024Nationwide• Akron Pharma, Inc.

Diphenhydramine HCl 25mg (Akron Pharma) – Incorrect Tablet Imprint (2024)

Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.

Class III

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Low

FDADec 12, 2024Nationwide• Akron Pharma, Inc.

Acetaminophen Regular Strength (Akron Pharma) – Incorrect Tablet Imprint (2024)

Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.

Class IIILow

FDADec 12, 2024Nationwide• Akron Pharma, Inc.

Acetaminophen Extra Strength 500mg (Akron Pharma) – Incorrect Tablet Imprint (2024)

Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.

Class IIILow

FDADec 12, 2024Nationwide• Akron Pharma, Inc.

Impella RP with SmartAssist (Abiomed) – Optical Sensor Damage (2024)

Optical Sensors have been damaged due to physical interaction between the inlet and another device resulting in a Placement Signal Not Reliable (PSNR) alarm and loss of Central Venous (CV) Placement Signal, Pulmonary Artery (PA) Placement Signal & Pulmonary Artery Pulse Index (PAPi) metrics. Abiomed is reinforcing that there is a risk of potential interaction between the tip of guidewires, indwelling central venous lines or devices and inlet of the Impella pumps listed above during the insertion, manipulation, and removal of those devices. The interaction may result in optical sensor damage, temporary pump stop, or permanent pump stop.

Moderate

FDADec 12, 2024Nationwide• Abiomed, Inc.

VidaSlim 90-day (Vidaslim Co.) – toxic yellow oleander (2024)

Due to the presence of Toxic yellow oleander

Class IHigh

FDADec 11, 2024Nationwide• Vidaslim Co.

Chlorpromazine Tablets 25mg (Glenmark) – Impurity Limit Exceeded (2024)

CGMP Deviations: N-Nitroso-Desmethyl Chlorpromazine impurity (NNDCI) were found to be failing per current FDA recommended limit.

Class IIModerate

FDADec 11, 2024Nationwide• Glenmark Pharmaceuticals Inc., USA

Chlorpromazine Tablets 10mg (Glenmark) – Impurity Limit Exceeded (2024)

CGMP Deviations: N-Nitroso-Desmethyl Chlorpromazine impurity (NNDCI) were found to be failing per current FDA recommended limit.

Class IIModerate

FDADec 11, 2024Nationwide• Glenmark Pharmaceuticals Inc., USA

Connie's Thin Crust Pizza (Palermo Villa) – plastic contamination (2024)

Foreign material (plastic)

Class IIModerate

FDADec 11, 2024IL, MN, WI• Palermo Villa, Inc

Neo-Tee T-Piece Resuscitator (Mercury Medical) – Flow Controller Defect (2024)

Gas powered emergency resuscitator has a circuit flow controller manufactured with an undersized spring, which may cause resuscitator not reach the high and low ends of the PIP and PEEP pressure ranges, which may cause a loss of positive pressure, impacting effective ventilation of the patient.

Moderate

FDADec 10, 2024Nationwide• Mercury Enterprises, Inc. dba Mercury Medical

Dapsone Gel 7.5% (VIONA) – Crystallization Issue (2024)

Crystallization

Class IIModerate

FDADec 10, 2024Nationwide• VIONA PHARMACEUTICALS INC

Dapsone Gel 7.5% (Viona) – Crystallization (2024)

Crystallization

Class IIModerate

FDADec 10, 2024Nationwide• VIONA PHARMACEUTICALS INC

Idylla Instrument (Biocartis) – False-Positive MSI-H Results (2024)

False-positive MSI-H results generated by the Idylla MSI Test.

Moderate

FDADec 10, 2024AL, CA, NJ +2 more• Biocartis Nv B 3 Generaal De Wittelaan 11 Mechelen Belgium

JMC5A Oxygen Concentrator (Jiangsu Jumao) – Fire Hazard Risk (2024)

Fire/Burn Risk

Oxygen concentrator may melt or catch on fire during use.

High

FDADec 9, 2024OH• JIANGSU JUMAO X-CARE MEDICAL EQUIPMENT CO LTD No

Bloody Mary Mix (Borsari) – undeclared fish and soy (2024)

Undeclared Allergen

Product contains undeclared fish (anchovy) and soy.

Class IIModerate

FDADec 9, 2024AL, AZ, CA +22 more• Borsari Food Company Inc

Portrait Core Services (GE Medical) – Patient Monitoring Software Failure (2024)

There is a software issue that can result in the loss of patient monitoring on the Portrait Central Viewer Application after 425 days of continuous run-time.

Moderate

FDADec 6, 2024Nationwide• GE Medical Systems, LLC