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. 2,643 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
2,643 in last 12 months

Showing 2562125640 of 29,505 recalls

Medical DeviceMarch 17, 2014· 3M Company - Health Care Business

Recalled Item: 3M" Steri-Vac" Gas Sterilizer/Aerators Recalled by 3M Company - Health Care...

The Issue: Recently, 3M received a single report of a potential exposure to Ethylene...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2014· Stryker Communications

Recalled Item: SHAPE ARM Recalled by Stryker Communications Due to During the use of the...

The Issue: During the use of the SHAPE Arm there is the potential for the monitor mount...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2014· Smiths Medical ASD, Inc.

Recalled Item: Smiths Medical HOTLINE¿ Fluid Warming Set L-70. Product Usage: intended...

The Issue: Injection port of the Set may leak blood/ IV fluids from the septum of the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2014· Stryker Communications

Recalled Item: SHAPE ARM Recalled by Stryker Communications Due to During the use of the...

The Issue: During the use of the SHAPE Arm there is the potential for the monitor mount...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2014· Philips Medical Systems, Inc.

Recalled Item: Digital Diagnost Recalled by Philips Medical Systems, Inc. Due to The...

The Issue: The footboard of Patient support for stitching can be fixed in upper...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2014· Stryker Communications

Recalled Item: SHAPE ARM Recalled by Stryker Communications Due to During the use of the...

The Issue: During the use of the SHAPE Arm there is the potential for the monitor mount...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2014· Smiths Medical ASD, Inc.

Recalled Item: Smiths Medical HOTLINE¿ Fluid Warming Set L-80. Product Usage: intended...

The Issue: Injection port of the Set may leak blood/ IV fluids from the septum of the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2014· Breg Inc

Recalled Item: Economy Elastic Knee Sleeve Open Recalled by Breg Inc Due to Breg is...

The Issue: Breg is recalling the Economy Elastic Knee Sleeve Open and K-Lite Knee 2...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2014· Breg Inc

Recalled Item: K-Lite Knee 2 Stays with Visco Recalled by Breg Inc Due to Breg is recalling...

The Issue: Breg is recalling the Economy Elastic Knee Sleeve Open and K-Lite Knee 2...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2014· Medtronic MiniMed Inc.

Recalled Item: Medtronic MiniMed Paradigm Insulin Infusion Pumps Recalled by Medtronic...

The Issue: Medtronic is recalling the Medtronic MiniMed Paradigm Insulin Infusion Pumps...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2014· Merit Medical Systems, Inc.

Recalled Item: Merit Custom Syringe Kit Recalled by Merit Medical Systems, Inc. Due to The...

The Issue: The products are labeled as sterile but were not sterilized.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2014· Roche Diagnostics Operations, Inc.

Recalled Item: Cobas c8000 Modular Analyzer Series Cobas c502 Recalled by Roche Diagnostics...

The Issue: The Initial Cassette Volume Check (ICVC) is not activated on the cobas c 502...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2014· Merit Medical Systems, Inc.

Recalled Item: Pressure Monitoring Tubing Recalled by Merit Medical Systems, Inc. Due to...

The Issue: The products are labeled as sterile but were not sterilized.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2014· Teleflex Medical

Recalled Item: 5/10/12 mm Weck¿ Vista" Optical Bladeless Laparoscopic Access Port Recalled...

The Issue: Complaints were received of leakage of insufflation gas through the device,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2014· Teleflex Medical

Recalled Item: 5/10 mm Weck¿ Recalled by Teleflex Medical Due to Complaints were received...

The Issue: Complaints were received of leakage of insufflation gas through the device,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2014· Teleflex Medical

Recalled Item: Sutures Recalled by Teleflex Medical Due to The products are being recalled...

The Issue: The products are being recalled because they did not meet minimum needle...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2014· Teleflex Medical

Recalled Item: 5/10 mm Weck Vista Universal Cannula Recalled by Teleflex Medical Due to...

The Issue: Complaints of leakage of insufflation gas through the device.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2014· Teleflex Medical

Recalled Item: Weck¿ Vista" Recalled by Teleflex Medical Due to Complaints were received of...

The Issue: Complaints were received of leakage of insufflation gas through the device,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2014· Teleflex Medical

Recalled Item: Weck¿ Vista" Universal Laparoscopic Port Recalled by Teleflex Medical Due to...

The Issue: Complaints were received of leakage of insufflation gas through the device,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2014· Teleflex Medical

Recalled Item: 5/10 Weck¿ Vista" Universal Balloon Open Access Port - Long Length (100mm)...

The Issue: Complaints were received of leakage of insufflation gas through the device,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing