Stay Informed

Get email alerts when new recalls match your interests.

Recall data is updated hourly from official government sources. Very recent recalls may not yet appear. About our data sources

About

We make U.S. recall data searchable and accessible for consumers and businesses.

Site

FAQ
Browse by State
Statistics
Recall Classifications
About
Enterprise API

Legal

Privacy Policy
Terms of Service
Report Incorrect Info

Official Sources

FDA Recalls ↗
USDA FSIS ↗
CPSC Recalls ↗
NHTSA Recalls ↗

RSS Feed

Home
/
Brands
/
Valeant Pharmaceuticals North America LLC

Valeant Pharmaceuticals North America LLC Recalls

All product recalls associated with Valeant Pharmaceuticals North America LLC.

Get alerts for this brand

Recall Summary

Total Recalls

709

Past Year

Class I (Serious)

Most Recent

Nov 2025

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 241–260 of 709 recalls

Cortaid Maximum Strength Cream (Valeant) – Microbial Contamination (2018)

CGMP deviations: Notice received from supplier of a voluntary recall of all their nasal products and baby oral gels due to the possibility of microbial contamination. No positive results for the firm's products. were obtained. After the firm review, cGMP deviations ere evident.

Class IIModerate

FDAAug 24, 2018Nationwide• Valeant Pharmaceuticals North America LLC

Cortaid Cooling Spray (Valeant) – Microbial Contamination (2018)

Class IIModerate

FDAAug 24, 2018Nationwide• Valeant Pharmaceuticals North America LLC

1...11 121314 15...36

Page 13 of 36Next

Cortaid Anti-itch Cream (Valeant) – Microbial Contamination (2018)

Class IIModerate

FDAAug 24, 2018Nationwide• Valeant Pharmaceuticals North America LLC

Diazepam Rectal Gel (Valeant) – Incorrect Labeling (2018)

Labeling: Incorrect or Missing Lot and/or Exp Date: Product distributed without a lot number or expiration date on the outer carton.

Class IIILow

FDAJul 10, 2018Nationwide• Valeant Pharmaceuticals North America LLC

Yamaha Golf Cars and PTVs (Yamaha) – crash hazard (2018)

This recall involves the following model year 2015 through 2018 gas and electric-powered golf cars , PTVs and utility vehicles. The vehicles were sold in various colors including blue, green, red, white, tan and silver. The model and serial numbers can be found on a label under the seat on the left or right side. Model Name Model Year Model Number Serial Number Range The DRIVE Models YDRA (Gas) 2015 JC0 0600101-0606900 JC2 0200101-0211800 JW8 0500101-0516400 2016 JC0 0700101-0706598 JC2 0300101-0312000 JW8 0600101-0614300 The DRIVE Models YDRE (Electric) 2015 JC1 0600101-0603300 JW9 0500101-0518300 2016 JC1 0700101-0703500 JC3 0000101-0004700 JW9 0600101-0618100 The DRIVE 2 Models DR2A (Gas) 2017 J0A 0000101-0010100 J0B 0000101-0016900 J0D 0000101-0007200 2018 J0A 0100101-0105300 J0B 0100101-0107287 J0D 0100101-0104700 The DRIVE 2 Models DR2E (Electric) 2017 J0C 0000101-0011400 J0E 0000101-0002900 J0J 0000101-0001999 2018 J0C 0100101-0105482 J0E 0100101-0101300 J0J 0100101-0100798

CPSCFeb 22, 2018Nationwide• Yamaha Motor Manufacturing Corporation of America, of Newnan, Ga.

HCG Methylcobalamin Injection (Compounding Pharmacy) – Non-Sterile (2018)

Non-Sterility

Class IHigh

FDAJan 12, 2018SC, TN• The Compounding Pharmacy of America

Baking Mix (Wel-Plan) - Contamination Risk (2017)

Nutricia North America, Inc. has decided to recall SHS Wel-Plan Baking Mix , 400 g box because testing of the product has detected a low level (0.74 cfu/g) contamination of Klebsiella pneumonia. The product is a baking mix and is intended to be cooked, which would kill K. pneumonia. The recall is being conducted out of an abundance of caution to avoid the risk that some consumers may misuse the product and consume it without cooking.

Class IIModerate

FDADec 21, 2017Nationwide• Nutricia North America

C-Therapy Night Cream (Valeant) – Incomplete Packaging (2017)

Labeling: Incorrect or Missing Package Insert - Obagi-C Rx System C-Therapy Night Cream is being recalled due to incomplete packaging/labeling. The bottle is missing the product insert and outer carton which contain the complete instruction for use and safety information.

Class IIILow

FDAJun 28, 2017Nationwide• Valeant Pharmaceuticals North America LLC

Kiteboard Control Systems (Cabrinha) – Injury Risk (2017)

Fire/Burn Risk

The component subject to recall is the stainless steel POWER BRACKET SEAT (PBS) and the lower front line that connects with the landing line on the Overdrive 1X Recoil with Fireball or Quickloop, Overdrive 1X Trimlite with Fireball or Quickloop, 1X Trimlite with Fireball or Quickloop and the Chaos 1X Control system models. The stainless steel PBS is mounted on the top of the depower mainline between one of the lower front lines and the landing line. The PBS is used as a stopping point for one of the flying lines while allowing the activation of the 1X security landing line. Model numbers included in the recall are: KS7CSODFR, KS7CSODQR, KS7CSODFC, KS7CSODQC, KS7CSFXFC, KS7CSFXQC and KS7CSCHFX. Only models with "2017 1X" printed on a cloth tab attached to the bungee line restrainers at the end of the bars are included in this recall.

CPSCMay 17, 2017Nationwide• Cabrinha Kites, a subsidiary of Pryde Group Americas, of Doral, Fla.

CLENZIderm Acne Treatment System (Valeant) – Product Discoloration (2017)

Discoloration.

Class IIILow

FDAMar 20, 2017Nationwide• Valeant Pharmaceuticals North America LLC

CLENZIderm Pore Therapy (Valeant) – Product Discoloration (2017)

Discoloration.

Class IIILow

FDAMar 20, 2017Nationwide• Valeant Pharmaceuticals North America LLC

KingQuad ATVs (Suzuki) – crash hazard (2016)

This recall involves model year 2016 and 2017 LT-A750X and LT-A750XP KingQuad ATVs. "Suzuki KingQuad" and "4x4 750AXi" are on decals on the sides. The model number is printed on a hang tag on the ATV and on the owner's manual. The XP model has power steering. They were sold in green, red, camouflage and black colors.

CPSCDec 28, 2016Nationwide• Suzuki Manufacturing of America Corporation, of Rome, Ga.

Galaxy Note7 Smartphones (Samsung) – battery fire risk (2016)

Fire/Burn Risk

This recall involves all Samsung Galaxy Note7 smartphones. The recalled devices have a 5.7-inch screen and were sold in the following colors: black onyx, blue coral, gold platinum and silver titanium with a matching stylus. Samsung is printed on the top front of the phone and Galaxy Note7 is printed on the back of the phone. This recall involves all Galaxy Note7 devices received as replacements as part of the previous Galaxy Note7 recall on September 15, 2016 and any Galaxy Note 7 with a green battery icon, regardless of date purchased or IMEI.

CPSCOct 13, 2016Nationwide• Samsung Electronics America Inc., of Ridgefield Park, N.J.

Galaxy Note7 Smartphone (Samsung) – Fire and burn hazard (2016)

Fire/Burn Risk

This recall involves the Samsung Galaxy Note7 smartphone sold before September 15, 2016. The recalled devices have a 5.7 inch screen and were sold in the following colors: black onyx, blue coral, gold platinum and silver titanium with a matching stylus. Samsung is printed on the top front of the phone and Galaxy Note7 is printed on the back of the phone. To determine if your phone has been recalled, locate the IMEI number on the back of the phone or the packaging, and enter the IMEI number into the online registration site www.samsung.com or call Samsung toll-free at 844-365-6197.

CPSCSep 15, 2016Nationwide• Samsung Electronics America Inc., of Ridgefield Park, N.J.

Seconal Sodium Capsules (Valeant) – missing anaphylaxis warning (2016)

Labeling: Incorrect or Missing Package Insert: Package insert is missing warning regarding anaphylaxis.

Class IIILow

FDAJun 10, 2016Nationwide• Valeant Pharmaceuticals North America LLC

Lodrane D (Valeant) – Mislabeled Carton Packaging (2016)

Labeling: Not Elsewhere Classified: correctly labeled bottles were packaged in cartons that were mislabeled with an incorrect active ingredient, phenylephrine rather than pseudoephedrine, on the carton face and carton top.

Class IIILow

FDAMay 23, 2016Nationwide• Valeant Pharmaceuticals North America LLC