Product Recalls in Georgia
Product recalls affecting Georgia — including food, drugs, consumer products, medical devices, and vehicles distributed to Georgia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,029 recalls have been distributed to Georgia in the last 12 months.
Showing 36761–36780 of 53,623 recalls
Recalled Item: Ziehm Vision RFD Recalled by Ziehm Imaging Inc Due to Malfunction of the...
The Issue: Malfunction of the radiation-warning timer and the 3D-specific interval...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kumpe Access Catheter Cathether Recalled by Cook Inc. Due to Increase in...
The Issue: Increase in reports of polymer degradation of the catheter tip, resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POROUS PATELLA 32MM X 10MM - 00587806532 POROUS PATELLA 35MM Recalled by...
The Issue: Zimmer Biomet is initiating a recall of specific lots of foil pouched,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VIDAS NT-pro-BNP Product Usage: VIDAS¿ NTproBNP (PBNP) is an automated...
The Issue: Due to a packaging error; The kit does not contain the correct number of C1...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: White Lumax Guiding Coaxial Catheter Catheter Recalled by Cook Inc. Due to...
The Issue: Increase in reports of polymer degradation of the catheter tip, resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: REV. SHELL LINER 0D 28X48 00700504828 REV. SHELL LINER 10D Recalled by...
The Issue: Zimmer Biomet is initiating a recall of specific lots of foil pouched,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beacon Tip Torcon NB Advantage Catheter Catheter Recalled by Cook Inc. Due...
The Issue: Increase in reports of polymer degradation of the catheter tip, resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ziehm Vision2 Recalled by Ziehm Imaging Inc Due to Malfunction of the...
The Issue: Malfunction of the radiation-warning timer and the 3D-specific interval...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volt Resistance Heated Lower Back Garment Deep penetrating heat garment...
The Issue: During an FDA inspection it was found that the firm claims unapproved...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TM CR TIB SZ 3 C-H Recalled by Zimmer Trabecular Metal Technology, Inc. Due...
The Issue: Zimmer Biomet is initiating a recall of specific lots of foil pouched,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ziehm Solo Recalled by Ziehm Imaging Inc Due to Malfunction of the...
The Issue: Malfunction of the radiation-warning timer and the 3D-specific interval...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TM MONO TIB STR GRN SZ 5 - 00588606510 TM Recalled by Zimmer Trabecular...
The Issue: Zimmer Biomet is initiating a recall of specific lots of foil pouched,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volt Resistance Heated Therapy Foot Wrap Deep penetrating heat garment...
The Issue: During an FDA inspection it was found that the firm claims unapproved...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volt Resistance Heated Neck Garment Deep penetrating heat garment and wraps...
The Issue: During an FDA inspection it was found that the firm claims unapproved...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ziehm Vision R Recalled by Ziehm Imaging Inc Due to Malfunction of the...
The Issue: Malfunction of the radiation-warning timer and the 3D-specific interval...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volt Resistance Heated Elbow Garment Deep penetrating heat garment and wraps...
The Issue: During an FDA inspection it was found that the firm claims unapproved...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FluoroSet Radiographic Tubal Assessment Set Cannula Recalled by Cook Inc....
The Issue: Increase in reports of polymer degradation of the catheter tip, resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volt Resistance Heated Therapy Shoulder Wrap Deep penetrating heat garment...
The Issue: During an FDA inspection it was found that the firm claims unapproved...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ziehm Vision RFD 3D Mobile C-arm for Mobile Fluoroscopic Imaging Recalled by...
The Issue: Malfunction of the radiation-warning timer and the 3D-specific interval...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neff DAgostino Percutaneous Access Set Accessories Recalled by Cook Inc. Due...
The Issue: Increase in reports of polymer degradation of the catheter tip, resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.