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Warner Chilcott Company LLC

Warner Chilcott Company LLC Recalls

All product recalls associated with Warner Chilcott Company LLC.

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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 20881–20900 of 25002 recalls

Femtrace 0.45mg Tablets (Warner Chilcott) – Moisture Ingress (2012)

Failed Impurity/Degradation Specifications due to moisture ingress in individual bottles

Class IIILow

FDADec 21, 2012Nationwide• Warner Chilcott Company LLC

2008 AIRSTREAM INTERSTATE Recall: ELECTRICAL SYSTEM

Fire/Burn Risk

Airstream is recalling certain model year 2008-2013 Interstate motorhomes manufactured August 2007, through December 2012 and equipped with the rear sofa floor plan. The electrical equipment underneath the sofa may come in contact with the seat belt buckle or metal cables from the seat.

NHTSADec 20, 2012Nationwide• AIRSTREAM

Diet Wild Cherry Pepsi (Pepsi) – Mislabeled Bottles (2012)

The labels on two-liter batches of Regular and Diet Wild Cherry Pepsi were mistakenly swapped during production. This is potential safety issue for individuals who are sensitive to phenylalanine (i.e., phenylketonuric) or who are diabetic.

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Class IIModerate

FDADec 20, 2012CT, ME, MA +2 more• Pepsi Cola North America

Regular Wild Cherry Pepsi (Pepsi) – Mislabeled Bottles (2012)

Class IIILow

FDADec 20, 2012CT, ME, MA +2 more• Pepsi Cola North America

Arctic Cat Bearcat Snowmobiles – fire risk (2012)

Fire/Burn Risk

The recall involves model year 2013 wide-track versions of the Arctic Cat Bearcat series. The Bearcat 570 XT and 570 WT have seats for an operator and a passenger. The model name and the letters "XT" or "WT" are on each side of the hood and the number "570" is near the rear of the tunnel on each side. Both vehicles have blue hoods. The Bearcat Z1 XT has seats for an operator and a passenger. The model name and the letters "XT" are on each side of the hood and "Z1" is near the rear of the tunnel on each side. It has a blue hood. The Bearcat Z1 XT GS is a single-rider vehicle. The model name and the letters "GS" are on each side of the hood and "Z1" is near the rear of the tunnel on each side. It has an orange hood, a winch on the front and a light bar located behind the operator's seat. The Bearcat Z1 XT LTD has seats for an operator and a passenger. The model name, the letters "XT" and the word "Limited" are on each side of the hood and "Z1" is near the rear of the tunnel on each side. It has a black hood and tunnel. Recalled vehicles have the last six digits of the vehicle identification number (VIN) in the following ranges: 808110 through 808130 and 108866 through 120615. The VIN appears on a sticker attached to the tunnel on the rider's right side and is also engraved in the same area.

CPSCDec 19, 2012Nationwide• Arctic Cat Inc., of Thief River Falls, Minn.

Polaris Pro-RMK Snowmobiles – serious injury (2012)

The recall involves 2013 Polaris Pro-RMK 600 and 800 snowmobiles. The snowmobiles come in red, white and black. "Pro-RMK" is on the lower right and left sides of the hood. The engine size and the letters "ES" or the words "Limited Edition" are on the upper right and left sides of the hood. The numbers "155" or "163" are on the rear of the tunnel. "Polaris" appears on the sides of the seat. The model number and serial number can be found on the right hand side of the tunnel below the seat. This recall includes the models listed below: Model Name Model Number 600 PRO RMK 155 S13CG6GSA 800 PRO RMK 163 S13CH8GSA 800 PRO RMK 163 ES S13CH8GSL

CPSCDec 18, 2012Nationwide• Polaris Industries Inc., of Medina, Minn.

Norco Havoc Bicycles – injury potential (2012)

This recall involves 2011 Havoc 24-inch and 26-inch bicycles. The 24-inch bicycles were sold in semi-matte grey and the 26-inch in semi-matte red. On some of the bicycles, "Norco" is printed on the firm's crest that is affixed to the head tube. Bicycle frames included in this recall have serial numbers that begin with K10DQ, K10FQ, K10IQ, K10KQ P10K, P10F or P11B. The serial number is stamped on the underside of the bottom bracket, below the word "Havoc."

CPSCDec 18, 2012Nationwide• Norco Bicycles, a division of LTP Sports Group Inc., of Port Coquitlam, British Columbia, Canada

Frozen Lobster Meat (Apollo) – Listeria Contamination (2012)

Listeria

The product or a previous product from this date code was found with Listeria monocytogenes through laboratory analysis.

Class IHigh

FDADec 18, 2012MA, NH• Cap Sur Mer, Inc.

Failed Dissolution Specification: Out of a specification result occurred during the 3-month stability testing. Dissolution result at the 4-hour time point was 41% (specification: 20-40%).

Class IIModerate

FDADec 18, 2012Nationwide• Watson Pharmaceuticals

Blue Diamond Pill (Performance Plus Marketing) – Undeclared Ingredients (2012)

Undeclared Allergen

Marketed Without an Approved NDA/ANDA: product may contain undeclared sildenafil, tadalafil and analogues of these FDA approved active ingredients, making them unapproved drugs

Class IHigh

FDADec 17, 2012Nationwide• Performance Plus Marketing, Inc.

Mojo Nights Supreme Capsules (Performance Plus Marketing) – Undeclared Ingredients (2012)

Undeclared Allergen

Marketed Without an Approved NDA/ANDA: product may contain undeclared sildenafil, tadalafil and analogues of these FDA approved active ingredients, making them unapproved drugs

Class IHigh

FDADec 17, 2012Nationwide• Performance Plus Marketing, Inc.

Libigrow Capsules (Performance Plus Marketing) – Undeclared Ingredients (2012)

Undeclared Allergen

Marketed Without an Approved NDA/ANDA: product may contain undeclared sildenafil, tadalafil and analogues of these FDA approved active ingredients, making them unapproved drugs

Class IHigh

FDADec 17, 2012Nationwide• Performance Plus Marketing, Inc.

Blue Diamond Platinum Capsules (Performance Plus Marketing) – Undeclared Ingredients (2012)

Undeclared Allergen

Marketed Without an Approved NDA/ANDA: product may contain undeclared sildenafil, tadalafil and analogues of these FDA approved active ingredients, making them unapproved drugs

Class IHigh

FDADec 17, 2012Nationwide• Performance Plus Marketing, Inc.

Exparel (Pacira Pharmaceuticals) – Subpotent Medication (2012)

Subpotent; bupivacaine

Class IIModerate

FDADec 17, 2012Nationwide• Pacira Pharmaceuticals, Inc.