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Gyma Laboratories Of Amer,Inc

Gyma Laboratories Of Amer,Inc Recalls

All product recalls associated with Gyma Laboratories Of Amer,Inc.

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Recall Summary

Total Recalls

1000

Past Year

558

Class I (Serious)

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 5341–5360 of 7757 recalls

Clonidine Base Micronized (Gyma) – Manufacturing Deviation (2014)

cGMP Deviations: GYMA laboratories Inc. has recalled multiple Active Pharmaceutical Ingredients manufactured in Italy upon receipt of a Rapid Alert Notification issued by The Italian Medicines Agency due to lack of good manufacturing practices.

Class IIModerate

FDAJul 9, 2014Nationwide• Gyma Laboratories Of Amer,Inc

Propranolol HCl (Gyma) – Manufacturing Deviation (2014)

Class IIModerate

FDAJul 9, 2014Nationwide• Gyma Laboratories Of Amer,Inc

Clonidine HCL (Gyma) – Manufacturing Deviation (2014)

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Class IIModerate

FDAJul 9, 2014Nationwide• Gyma Laboratories Of Amer,Inc

Dipyridamole API (Gyma) – Manufacturing Deviation (2014)

Class IIModerate

FDAJul 9, 2014Nationwide• Gyma Laboratories Of Amer,Inc

Cumberland Cheese (Sequatchie Cove) – E. Coli Contamination (2014)

Sample of cheese taken by FDA was found to contain generic E Coli.

Class IIModerate

FDAJul 7, 2014TN• Ledgendairy Cheeseworks, LLC DBA Sequatchie Cove Creamery

BRAKE PARTS ACDELCO 17589B Equipment Recall: SERVICE BRAKES, AIR:DRUM:SHOES/LININGS

Brake Parts Inc, (BPI) is recalling certain ACDelco Part Nos. 17855B, 14855B, B855L, 17960B, 17815B, 14815B, B815L, 178589B, and 14589B, Carquest Part Nos. BS855, BS960, BS815, and BS589, Federated Part Nos. BS855, BS960, BS815, and BS589, and Raybestos Part Nos. 855PG, 855SG, 960PG, 815PG, 815SG, 589PG, and 589SG rear wheel brake shoes manufactured April 1, 2013 to April 19, 2014. The affected brake shoes may experience detachment from the steel shoe during operation.

NHTSAJul 3, 2014Nationwide• BRAKE PARTS

Diltiazem HCl Extended-release Capsules (Mylan) – Impurity Specification Failure (2014)

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

Class IIILow

FDAJul 3, 2014Nationwide• Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Fixed-Base Router (Porter-Cable) – Electrical Shock Risk (2014)

Four Porter-Cable 3 1/4 horsepower, electric, fixed-base production routers and one production router base are being recalled. The recalled routers are about 11 inches tall and 7 inches wide. The top of the router motor is black plastic and has the on/off switch for the router. The base is painted gray and has two side handles, an adjuster ring on the top and a clamp screw on the rear. The side handles on the base of recalled routers have no insulation. The Porter-Cable name and logo are on the front of the base. The recalled routers and base were manufactured from 1990 to April 2014. The following router models are being recalled: Model Number Speed/Feature 7518 5-speed 7519 1-speed 7519EC 1-speed/has an extended chuck 22-7519-60 1-speed/ uses 220-volt power source The router model number and the manufacture date code are on a metal plate on the back of the upper motor housing. The date code consists of the year of manufacture, the week of manufacture and the manufacturing plant code in the YYYY WW-XX format. The router base is model number 75361 and is also sold separately. The model number is located on the side of the base opposite the Porter-Cable label.

CPSCJul 2, 2014Nationwide• Black & Decker (U.S.) Inc., dba Porter-Cable, Towson, Md.

E-Z-HD Barium Sulfate (Bracco) – Subpotent Drug Concerns (2014)

Subpotent Drug: Low out of specification results for both pH and assay obtained during routine stability testing after 36 months.

Class IIILow

FDAJul 2, 2014Nationwide• Bracco Diagnostic Inc

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.

TranSmart Raspberry Cookie Dough (CSM Bakery) – Peanut Allergen (2014)

Undeclared Allergen

Undeclared Allergen; Peanuts.

Class IHigh

FDAJun 26, 2014AL, FL, GA +11 more• CSM Bakery Products NA-Atlanta Frozen

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.

Famotidine Oral Suspension (Novel Laboratories) – Stability Failure (2014)

Failed Impurity/Degradation Specification; 12-month stability time point

Class IIILow

FDAJun 20, 2014Nationwide• Novel Laboratories, Inc.

Glider Rockers (Brooks Furniture) – fall hazard (2014)

The recall includes two styles of Brooks Furniture glider rockers 1529P and 1529V-LM. The 1529P glider rocker has a maple wood frame with blue fabric upholstery. The 1529V-LM glider rocker has a maple wood frame with beige vinyl upholstery and a locking mechanism to disengage the glider. Both recalled chairs have the style number and manufacture date between 1/1/2011 and 12/31/2012 printed under the chair's seat. Brooks Furniture is printed on a label attached to the seat cushions.

CPSCJun 18, 2014Nationwide• Brooks Furniture Mfg. Inc. of Tazewell, Tenn.

Brevibloc (Baxter) – Particle Contamination (2014)

Presence of Particulate Matter: Complaints received of discolored solution identified as subvisible particles of iron oxide that are agglomerating.

Class IIModerate

FDAJun 16, 2014Nationwide• Baxter Healthcare Corp.

Venlafaxine (Caraco) – Dissolution Failure (2014)

Failed Dissolution Specifications: Stability results found the product did not meet the drug dissolution specifications.

Class IIModerate

FDAJun 12, 2014Nationwide• Caraco Pharmaceutical Laboratories, Ltd.

MXB Crossbows (Mission Archery) – Injury Hazard (2014)

Fire/Burn Risk

This recall involves Mission Archery crossbows that have the automatic safety located behind the trigger at rear of scope mount, models MXB 320, MXB Dagger, MXB 400 and MXB 360; and serial numbers ranging from XB04879 to XB16555. The crossbows were sold in black, lost camo AT (a three-color camouflage pattern with light brown, dark brown, dark green), white camo and pink camo pattern. The crossbows measure between 29 and 35 inches long and were available individually or as part of a package that included a black scope, quiver, three bolts and a rope cocking aid. Mission by Mathews is engraved on the left rear side of the crossbow's rail. The serial number is located on the underside of the rail directly behind the safety. Mission and the model name are printed on each limb.

CPSCJun 3, 2014Nationwide• Mathews Archery Inc., dba Mission Archery, of Sparta, Wis.

Roasted Garlic Fettuccine (Ronzoni) – Undeclared Soy (2014)

Undeclared Allergen

The firm initiated this recall as a precaution out of concern that the product contains an undeclared allergen soy. Even though the product may contain a very small amount of soy, it has been further processed so there is no detectable level of soy protein.

Class IIModerate

FDAJun 2, 2014CA, CT, FL +9 more• EBRO North America dba New World Pasta

HCG (Brookfield) – Incorrect Solvent (2014)

Undeclared Allergen

Incorrect/Undeclared Excipients: Specific drug products were compounded with an incorrect solvent.

Class IIModerate

FDAMay 30, 2014WI• Brookfield Prescription Center Inc. dba MD Custom Rx

HCG 125U/Tab Tablet (MD Custom Rx) – incorrect solvent (2014)

Undeclared Allergen

Incorrect/Undeclared Excipients: Specific drug products were compounded with an incorrect solvent.

Class IIModerate

FDAMay 30, 2014WI• Brookfield Prescription Center Inc. dba MD Custom Rx