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Caraco Pharmaceutical Laboratories Ltd.

Caraco Pharmaceutical Laboratories Ltd. Recalls

All product recalls associated with Caraco Pharmaceutical Laboratories Ltd..

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Recall Summary

Total Recalls

1000

Past Year

100

Class I (Serious)

Most Recent

Dec 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 1941–1960 of 2670 recalls

Oxcarbazepine Tablets (Caraco) – Broken Tablets (2014)

Failed Tablet Specifications: Broken Tablets Present.

Class IIModerate

FDAJan 29, 2014Nationwide• Caraco Pharmaceutical Laboratories Ltd.

Metformin HCl Extended-Release (Caraco) – Foreign Tablet Contamination (2014)

Presence of Foreign Tablet; customer complaint of some tablets of Gabapentin found in a bottle of Metformin HCl ER

Class IIModerate

FDAJan 28, 2014Nationwide• Caraco Pharmaceutical Laboratories, Ltd.

Carisoprodol Tablets (Mylan) – Impurity Specification Failure (2014)

Failed Impurity/degradation Specification

Class III

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Low

FDAJan 28, 2014Nationwide• Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Golden Natural Fruit Island (Crown Food) – Undeclared Sulfites (2014)

Undeclared Allergen

NYSDAM analysis has revealed the presence of undeclared sulfites and undeclared FD&C Yellow #6 in Golden Natural Brand "Fruit Island".

Class IHigh

FDAJan 27, 2014NJ, NY• Crown Food Distributors Inc

Hydrocodone Acetaminophen Tablets (Watson) – broken tablets (2014)

Failed Tablet/Capsule Specifications; Product contains broken tablets.

Class IIModerate

FDAJan 15, 2014AZ, CA, CT +8 more• Watson Laboratories Inc

Lansoprazole Capsules (Dr. Reddy's) – Microbial Contamination (2014)

Microbial Contamination of Non-Sterile Products: Out-of-specification results for microbial count were observed at the initial stability interval for Lansoprazole Delayed Release Capsules.

Class IIModerate

FDAJan 3, 2014Nationwide• Dr. Reddy's Laboratories, Inc.

MERITOR REMAN AXLES FOR TRAC INTE Equipment Recall: SUSPENSION:REAR:AXLE:NON-POWERED AXLE ASSEMBLY

Meritor, Inc. is recalling certain RMT14512ABS and RMT14612 trailer axles that were remanufactured for Trac Intermodal between June 1, 2013 and June 30, 2013. During remanufacturing, the axles may have been assembled with the lock washer and pin misaligned.

NHTSADec 24, 2013Nationwide• MERITOR

Carisoprodol Tablets (Watson Laboratories) – Metal Particulates (2013)

Presence of Foreign Substance; metal particulates were visually observed in the tablets.

Class IIModerate

FDADec 23, 2013Nationwide• Watson Laboratories Inc

Diclofenac Sodium Tablets (Watson) – Tablet Split Issue (2013)

Failed Tablet/Capsule Specifications: Split tablets were found in the 12-month stability samples.

Class IIModerate

FDADec 20, 2013Nationwide• Watson Laboratories, Inc.-(Actavis) - Florida

Mountain Bike Suspension Forks (Fox Factory) – Fall Hazard (2013)

The recalled suspension forks are model year 2013, 32 and 34 Evolution Series with 120mm to 160mm of travel. The Evolution name and logo are on a sticker on the front fork with the FOX brand name logo. Recalled forks can be identified by the serial number, which is found on the underside of the crown after removing the front wheel. The forks were sold as original equipment on some of the following 2013 model year mountain bikes: BMC, Cannondale, Commencal, Diamondback, GT, Kona, Lapierre, Norco, Orbea, Raleigh, Rocky Mountain, Santa Cruz, Scott, Specialized and Trek. A small quantity of suspension forks were sold to retailers or distributors as aftermarket accessories.

CPSCDec 18, 2013Nationwide• Fox Factory, of Watsonville, Calif.

Curl Activator Gel (Long Aid) – Cloudy Appearance (2013)

Product has a cloudy appearance

Class IIILow

FDADec 13, 2013CA, CT, FL +7 more• Keystone Laboratories Inc

Metoprolol Succinate Tablets (Dr. Reddy's) – Dissolution Issue (2013)

Failed Dissolution Specification; 12-Month stability interval.

Class IIModerate

FDADec 13, 2013LA, MI, MS +2 more• Dr. Reddy's Laboratories, Inc.

Movement and Sound Baby Monitors (Angelcare) – strangulation risk (2013)

The recall involves the Movement and Sound Monitor manufactured by Angelcare. This design of baby monitor includes a unique sensor pad placed inside the crib, under the mattress, to monitor movement of the baby. An electrical cord about 11 feet long is permanently connected from the sensor pad to the nursery monitor unit. The hazard is created by a cord within reach of a baby inside the crib. The cord can be pulled into the crib and can wrap around the child's neck. The recall involves all versions of Angelcare sensor monitors including model numbers: AC1100, AC201, AC300, AC401 AC601 and 49255 that did not include rigid cord covers, offered in the remedy. The model number is located on the back of the nursery monitor unit. The monitors were manufactured between 1999 and 2013.

CPSCNov 21, 2013Nationwide• Angelcare Monitors Inc.®, of Quebec, Canada

ONEBODE Flo Daily (Global Health) – antibiotic contamination (2013)

The finished dietary supplement product was manufactured with ingredients found to be contaminated with chloramphenicol, an antibiotic, above levels of 0.3 ppb.

Class IIModerate

FDANov 7, 2013AZ• Global Health Laboratories, LLC

UT-Fem Supplement (Global Health Laboratories) – Antibiotic Contamination (2013)

The finished dietary supplement product was manufactured with ingredients subsequently found to be contaminated with chloramphenicol, an antibiotic, at levels above 0.3 ppb. The supplier, Specialty Enzymes & Biotechnologies, recalled the raw materials and notified the recipients. Subsequent private laboratory testing of the finished product revealed levels of chloramphenicol above 0.3 ppb.

Class IIModerate

FDANov 7, 2013NY• Global Health Laboratories, LLC

Fruit Truffles (Torn Ranch) – Undeclared Yellow Color (2013)

FDA inspection at the firm found that Yellow # 5 and 6 used in decoration on top of fruit truffles was not declared in the ingredient statement.

Class IIModerate

FDAOct 25, 2013CA, FL, IN +7 more• Torn Ranch Inc.

Tri-Mins Supplement (Empirical Labs) – Chloramphenicol risk (2013)

Empirical Labs is recalling certain lots of dietary supplements due to potential for adulteration with chloramphenicol.

Class IIModerate

FDAOct 21, 2013ID, MN, SC +1 more• Empirical Laboratories, Incorporated

Vive Chocolate Shake (Empirical Labs) – Chloramphenicol risk (2013)

Empirical Labs is recalling certain lots of dietary supplements due to potential for adulteration with chloramphenicol.

Class IIModerate

FDAOct 21, 2013ID, MN, SC +1 more• Empirical Laboratories, Incorporated

P&L Enzymes Supplement (Empirical Labs) – Chloramphenicol risk (2013)

Empirical Labs is recalling certain lots of dietary supplements due to potential for adulteration with chloramphenicol.

Class IIModerate

FDAOct 21, 2013ID, MN, SC +1 more• Empirical Laboratories, Incorporated

Digesti-Zyme (Empirical Labs) – Chloramphenicol Risk (2013)

Empirical Labs is recalling certain lots of dietary supplements due to potential for adulteration with chloramphenicol.

Class IIModerate

FDAOct 21, 2013ID, MN, SC +1 more• Empirical Laboratories, Incorporated