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Gaymar Industries Inc

Gaymar Industries Inc Recalls

All product recalls associated with Gaymar Industries Inc.

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

145

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 35861–35880 of 37661 recalls

Gaymar Industries Inc: XPRT Therapy Mattress Systems: Model # 2950-000-000 with...

Design control/validation deficiencies.

FDAOct 25, 2004HI, IN, NE• Gaymar Industries Inc

Boston Scientific Corp: NAMIC Custom Angiographic Kit, Left Heart Kit. - . Mode...

The kits contains defective Magellan Monoject Safety Needles. The needle shaft may separate from the hub. Tyco Healthcare has recalled the needles.

FDAOct 21, 2004IL, IN, NV• Boston Scientific Corp

Beefmaster Explorer Outdoor Gas Grill (Nexgrill) – Pressure Regulator Problem (2004)

Fire/Burn Risk

This recall involves the Beefmaster Explorer Outdoor Gas Grill Model Number 720-0001. The tabletop grill is made of stainless steel and is used with a disposable propane cylinder, which is purchased separately. Each grill has one main burner and a cooking grid that sits over the burner. Model numbers are located on the back panel of the grill. The brand name "Nexgrill" is on a plate on the grill lid.

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CPSCOct 21, 2004Nationwide• Nexgrill Industries Inc., of Walnut, Calif.

Polaris RANGER 4x4 Utility Vehicle (Polaris) – Vehicle Safety Concern (2004)

All model year 2005 "RANGER 4x4" Utility Vehicles with model number R05RD50AA are part of this recall. The model number is located on the upper right frame tube directly under the right side of the seat. The RANGER 4x4 Utility Vehicles have black seats with a green chassis. "RANGER 4x4" is prominently displayed on the right and left side of the rear cargo box.

CPSCOct 21, 2004Nationwide• Polaris Industries, Inc., of Medina, Minn.

Boston Scientific Corp: NAMIC Custom Angiographic Kit, Left Heart Kit - . Model...

The kits contain defective Magellan Monoject Safety Needles. The needle shaft may separate from the hub. Tyco Healthcare has recalled the needles.

FDAOct 21, 2004IL, IN, NV• Boston Scientific Corp

General Electric Med Systems LLC: Patient tables of CT systems with brand name: CT/e; CT/e ...

The patient tables of the affected CT systems are supported by a hydraulic cylinder and a cylinder shaft (i.e. the upper shaft) which connects the tabletop to the table frame. GE received a report of a HiSpeed LX/I system table falling abruptly due to the filure of the upper shaft. No injuries were reported.

FDAOct 21, 2004Nationwide• General Electric Med Systems LLC

BD Diagnostic Systems: BD, Brucella melitensis Antigen

Febrile Antigens and Control Antisera that were released prior to August 2003 contained the 12/2000 revised insert that had incorrect testing instructions.

FDAOct 20, 2004Nationwide• BD Diagnostic Systems

BD Diagnostic Systems: BD, Salmonella O Group B Antigen (1-4-5-12)

Febrile Antigens and Control Antisera that were released prior to August 2003 contained the 12/2000 revised insert that had incorrect testing instructions.

FDAOct 20, 2004Nationwide• BD Diagnostic Systems

BD Diagnostic Systems: BD, Salmonella O Group A Antigen (1-2-12)

Febrile Antigens and Control Antisera that were released prior to August 2003 contained the 12/2000 revised insert that had incorrect testing instructions.

FDAOct 20, 2004Nationwide• BD Diagnostic Systems

BD Diagnostic Systems: BD, Proteus OX19 Antigen

Febrile Antigens and Control Antisera that were released prior to August 2003 contained the 12/2000 revised insert that had incorrect testing instructions.

FDAOct 20, 2004Nationwide• BD Diagnostic Systems

BD Diagnostic Systems: BD, Salmonella O Group D Antigen (9-12) (Typhoid O)

Febrile Antigens and Control Antisera that were released prior to August 2003 contained the 12/2000 revised insert that had incorrect testing instructions.

FDAOct 20, 2004Nationwide• BD Diagnostic Systems

BD Diagnostic Systems: BD, Salmonella Flagellar Polyvalent Antiserum (a,b,d)

Febrile Antigens and Control Antisera that were released prior to August 2003 contained the 12/2000 revised insert that had incorrect testing instructions.

FDAOct 20, 2004Nationwide• BD Diagnostic Systems

BD Diagnostic Systems: BD, Brucella abortus Antigen

Febrile Antigens and Control Antisera that were released prior to August 2003 contained the 12/2000 revised insert that had incorrect testing instructions.

FDAOct 20, 2004Nationwide• BD Diagnostic Systems

BD Diagnostic Systems: BD, Proteus Polyvalent Antiserum (OXK, OX2, OX19)

Febrile Antigens and Control Antisera that were released prior to August 2003 contained the 12/2000 revised insert that had incorrect testing instructions.

FDAOct 20, 2004Nationwide• BD Diagnostic Systems

BD Diagnostic Systems: BD, Brucella Postive Control Antiserum (AMS)

Febrile Antigens and Control Antisera that were released prior to August 2003 contained the 12/2000 revised insert that had incorrect testing instructions.

FDAOct 20, 2004Nationwide• BD Diagnostic Systems

BD Diagnostic Systems: BD, Salmonella Flagellar d Antigen (Typhoid H)

Febrile Antigens and Control Antisera that were released prior to August 2003 contained the 12/2000 revised insert that had incorrect testing instructions.

FDAOct 20, 2004Nationwide• BD Diagnostic Systems

Chenille Mattress Pad (Chris Arlotta) – Product Safety Issue (2004)

Fire/Burn Risk

The recalled mattress pads are natural colored, made of 100 percent cotton Chenille, and were sold in twin, full, queen, king and California king. The Web and catalog retailers and the mattress pads' model numbers, listed below, are identified on the packaging: Web Retailer Style Numbers The Vermont Country Store 242637, 42638, 42639, 42640 Garnet Hill Inc 066-TW, 066-DB, 066-QN, 066-KG, 066-CK GAIAM Inc 03-0144T, 03-0144F, 03-0144Q, 03-0144K, S5224 The Company Store MA0501T, MA0501F, MA0501Q, MA0501K

CPSCOct 20, 2004Nationwide• Chris Arlotta Enterprises Ltd., of New York, N.Y.

BD Diagnostic Systems: BD, Francisella tularensis Antigen

Febrile Antigens and Control Antisera that were released prior to August 2003 contained the 12/2000 revised insert that had incorrect testing instructions.

FDAOct 20, 2004Nationwide• BD Diagnostic Systems

Medtronic Inc. Cardiac Rhythm Managment: Medtronic CapSureFix Novus Lead Model 5076.

A specific lot of leads are labeled incorrectly. The leads are 45 cm in length and labeled as 52 cm lead length.

FDAOct 20, 2004Nationwide• Medtronic Inc. Cardiac Rhythm Managment

BD Diagnostic Systems: BD, Febrile Antigen Negative Control

Febrile Antigens and Control Antisera that were released prior to August 2003 contained the 12/2000 revised insert that had incorrect testing instructions.

FDAOct 20, 2004Nationwide• BD Diagnostic Systems