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American Health Packaging

American Health Packaging Recalls

All product recalls associated with American Health Packaging.

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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 18881–18900 of 25002 recalls

Ibuprofen Tablets 600mg (American Health) – Labeling Mix-Up (2014)

Labeling: Label Mix-Up: Some cartons of AHP Ibuprofen Tablets, USP, 600mg, lot #142588 that contain blister cards filled with Ibuprofen tablets, 600mg drug product, were found to be mis-labeled with blister card print identifying the product as AHP Oxcarbazepine Tablets, 300mg, lot #142544

Class IHigh

FDAJul 1, 2014Nationwide• American Health Packaging

Oxcarbazepine Tablets 300mg (American Health) – Labeling Mix-Up (2014)

Class IHigh

FDAJul 1, 2014Nationwide• American Health Packaging

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Cephalexin Capsules 500mg (Caraco) – Manufacturing Deviation (2014)

CGMP Deviations: These products are being recalled because they were manufactured with active pharmaceutical ingredients (APIs) that were not manufactured with good manufacturing practices.

Class IIModerate

FDAJun 26, 2014Nationwide• Caraco Pharmaceutical Laboratories, Ltd.

Poly-Tussin AC Liquid (Poly Pharmaceuticals) – Monograph Deviation (2014)

Does Not Meet Monograph: Phenylephrine and pseudoephedrine are below monograph specifications, and label inaccurately contains wording "Rx Only".

Class IIILow

FDAJun 26, 2014Nationwide• Poly Pharmaceuticals, Inc

Cephalexin Capsules 250mg (Caraco) – Manufacturing Deviation (2014)

CGMP Deviations: These products are being recalled because they were manufactured with active pharmaceutical ingredients (APIs) that were not manufactured with good manufacturing practices.

Class IIModerate

FDAJun 26, 2014Nationwide• Caraco Pharmaceutical Laboratories, Ltd.

Lortuss EX Liquid (Poly Pharmaceuticals) – Monograph Deviation (2014)

Does Not Meet Monograph: Phenylephrine and pseudoephedrine are below monograph specifications, and label inaccurately contains wording "Rx Only".

Class IIILow

FDAJun 26, 2014Nationwide• Poly Pharmaceuticals, Inc

Ascorbic Acid Injection (Pharmacy Creations) – Mold Contamination (2014)

Non-Sterility: Pharmacy Creations is recalling Ascorbic Acid 500 mg/mL 50 mL vials due to mold contamination.

Class IHigh

FDAJun 25, 2014NJ, NY, PR• Pharmacy Creations

Tern Folding Bicycles (Stile Products) – Fall Hazard (2014)

The recall involves Link Uno, Link D7i, Link D8, Link P9, Link P7i, and Link P24h models of Tern brand adult folding bikes. These six models were sold in black/blue, black/green, black/gray, black/red dark gray/light gray, gray/orange and white/pink color combinations. "Tern" is printed on the front end of the top tube and on other portions of the frame. The model name is printed on the middle of the top tube. Recalled bicycles have a 10-character alphanumeric serial number that begin with either AI1133 through AI1137 or AI1149 through AI1213 stamped on the bottom bracket shell of the bike. An alphanumeric service tag number is located on the front of the seat tube and this number can be used to determine if the bicycle is affected by going to the firm's website.

CPSCJun 24, 2014Nationwide• Taicang A&I Medical Appliances Co., of Jiangsu, China

Tolterodine Tartrate Tablets (Mylan) – Impurity Specification Failure (2014)

Failed Impurities/Degradation Specifications; Out of specification for lactol and total impurities.

Class IIILow

FDAJun 20, 2014Nationwide• Mylan Pharmaceuticals Inc.

Goalie Throat Collars (Reebok-CCM) – Laceration Risk (2014)

Laceration Risk

The recalled Reebok TCPRE Senior (SR) and Junior (JR) Goalie Throat Collars are black with white trim and the word "Reebok" is embroidered at the base of the collar. They have the BNQ certification mark screen printed and the words "Ballistic Nylon Ballistique", "TCPRE SR or JR" and sizing information on the right side of the collar base. Affected products have the model number K101SR TCPRE or K101JR TCPRE located on the label sewn on the inside of each throat collar pad and on the outside of a polybag in which the product may have been sold at retail stores.

CPSCJun 19, 2014Nationwide• Sport Maska Inc. of Montreal, Quebec, Canada

Diltiazem HCl Extended Release Capsules (Mylan) – Compound Failure (2014)

Failed Impurities/Degradation Specifications: High out-of-specification results for a related compound obtained during routine stability testing.

Class IIILow

FDAJun 19, 2014Nationwide• Mylan Pharmaceuticals Inc.

Bystolic Tablets (Forest Pharmaceuticals) – Dissolution Failure (2014)

Failed Dissolution Specifications: Drug failed stage III dissolution testing.

Class IIModerate

FDAJun 19, 2014Nationwide• Forest Pharmaceuticals Inc

Frederick Farms Chocolate Ice Cream (Garber) – incorrect lid (2014)

The firm used the wrong lid on end of production run on Frederick Farms 4oz regular Chocolate Ice Cream. The wrong lid used was Frederick Farm NSA (No Sugar Added) Chocolate Ice Cream.

Class IIModerate

FDAJun 18, 2014MD, PA, VA +1 more• Garber Ice Cream Company Inc

2013 AMERICAN COACH AMERICAN EAGLE – allied recreation group, inc (2014)

Allied Recreation Group, Inc. (Allied) is recalling certain model year 2013-2014 American Coach-brand American Eagle and American Revolution and certain 2013 American Tradition motor homes equipped with certain Villa ISS GSK powered driver and passenger seats. The seat belt attachment may be incorrect and the seat belt may fray if it rubs along a steel bracket in the seat, reducing its strength. As such, these seats do not conform to Federal Motor Vehicle Safety Standard (FMVSS) number 209, "Seat Belt Assemblies."

NHTSAJun 17, 2014Nationwide• AMERICAN COACH

2015 AMERICAN COACH AMERICAN EAGLE – allied recreation group (2014)

Allied Recreation Group. Inc. (Allied) is recalling certain model year 2015 American Coach-brand American Eagle, American Tradition and American Revolution motor homes equipped with certain Villa ISS powered driver and passenger GSK seats. The seat belt attachment may be incorrect and the seat belt may fray if it rubs along a steel bracket in the seat, reducing its strength. As such, these seats do not conform to Federal Motor Vehicle Safety Standard (FMVSS) number 209, "Seat Belt Assemblies."

NHTSAJun 17, 2014Nationwide• AMERICAN COACH

Apri (Teva) – Impurity Specification Failure (2014)

Failed Impurities/Degradation Specifications: out of specification impurity test results.

Class IIILow

FDAJun 17, 2014Nationwide• Teva Pharmaceuticals USA

Mircette (Teva) – Impurity Specification Failure (2014)

Failed Impurities/Degradation Specifications: out of specification impurity test results.

Class IIILow

FDAJun 17, 2014Nationwide• Teva Pharmaceuticals USA

Kariva (Teva) – Impurity Specification Failure (2014)

Failed Impurities/Degradation Specifications: out of specification impurity test results.

Class IIILow

FDAJun 17, 2014Nationwide• Teva Pharmaceuticals USA

Velivet (Teva) – Impurity Specification Failure (2014)

Failed Impurities/Degradation Specifications: out of specification impurity test results.

Class IIILow

FDAJun 17, 2014Nationwide• Teva Pharmaceuticals USA

Wegmans Cinnamon Raisin Buns (Wegmans) – Undeclared Eggs (2014)

Undeclared Egg

The Raisin Cinnamon Buns contain undeclared eggs which may also be raw. This poses a potential health risk to consumers if the product is consumed.

Class IHigh

FDAJun 14, 2014MD, MA, NJ +3 more• Wegmans Food Markets, Inc.