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. 2,743 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
2,743 in last 12 months

Showing 1656116580 of 29,505 recalls

Medical DeviceMay 9, 2018· Johnson & Johnson Surgical Vision Inc

Recalled Item: OptiMedica Catalys Precision Laser System Recalled by Johnson & Johnson...

The Issue: Software upgrade exhibits failures when executing Daily Alignment...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2018· Wescam Inc

Recalled Item: MX-10 surveillance laser system Product Usage: The expected usage of...

The Issue: Product has a nominal ocular hazard distance (NOHD) that is longer than...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2018· Vyaire Medical

Recalled Item: AirLife Resuscitation Device Recalled by Vyaire Medical Due to An error in...

The Issue: An error in manufacturing of the AirLife Resuscitation Devices that has the...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 8, 2018· Vyaire Medical

Recalled Item: AirLife Resuscitation Device Recalled by Vyaire Medical Due to An error in...

The Issue: An error in manufacturing of the AirLife Resuscitation Devices that has the...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 8, 2018· Human Design Medical Llc

Recalled Item: Vivo 65 Recalled by Human Design Medical Llc Due to Some Vivo 65 devices...

The Issue: Some Vivo 65 devices have an unreleased version of the Firmware upgrade tool.

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

Class III — Low RiskOngoing
Medical DeviceMay 8, 2018· Stryker Sustainability Solutions

Recalled Item: Reprocessed HARMONIC Ace¿ +7 Recalled by Stryker Sustainability Solutions...

The Issue: Stryker Sustainability Solutions has received an increase in reports...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2018· Zeiss, Carl Inc

Recalled Item: Cell Observer SD Recalled by Zeiss, Carl Inc Due to In certain eyepiece...

The Issue: In certain eyepiece configurations the laser shutter may not close...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2018· Baxter Healthcare Corporation

Recalled Item: Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 8)...

The Issue: The firm will be updating the Instructions for Use for the product. Current...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2018· Baxter Healthcare Corporation

Recalled Item: Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 6)...

The Issue: The firm will be updating the Instructions for Use for the product. Current...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2018· Roche Diabetes Care, Inc.

Recalled Item: Accu-Chek Performa Test Strip Recalled by Roche Diabetes Care, Inc. Due to...

The Issue: The recalling firm has identified two lots of test strips that are out of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2018· Ethicon, Inc.

Recalled Item: PROLENE SUTURE 30"(75CM) 6-0 BLUE Recalled by Ethicon, Inc. Due to The...

The Issue: The needle associated with certain suture product codes has the potential to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2018· Ethicon, Inc.

Recalled Item: PROLENE SUTURE BLUE 4X90CM M1.5 USP 4/0 DA RB-1 +P Recalled by Ethicon, Inc....

The Issue: The needle associated with certain suture product codes has the potential to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2018· Ethicon, Inc.

Recalled Item: PROLENE SUTURE 24"(60CM) 7-0 BLUE Recalled by Ethicon, Inc. Due to The...

The Issue: The needle associated with certain suture product codes has the potential to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2018· Ethicon, Inc.

Recalled Item: PROLENE SUTURE MONO BLUE BV1755 Taperpoint 3/8C Recalled by Ethicon, Inc....

The Issue: The needle associated with certain suture product codes has the potential to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2018· Ethicon, Inc.

Recalled Item: PROLENE SUTURE MONO BLUE - BV1755 Taper Point 3/8C Recalled by Ethicon, Inc....

The Issue: The needle associated with certain suture product codes has the potential to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2018· Ethicon, Inc.

Recalled Item: PROLENE SUTURE BLUE 18" 7-0 D/A BV-1 Recalled by Ethicon, Inc. Due to The...

The Issue: The needle associated with certain suture product codes has the potential to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2018· Ethicon, Inc.

Recalled Item: PROLENE SUTURE 4-36"(90CM) 4-0 BLUE Recalled by Ethicon, Inc. Due to The...

The Issue: The needle associated with certain suture product codes has the potential to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2018· Ethicon, Inc.

Recalled Item: PROLENE SUTURE 4-36" (90CM) 3-0 BLUE Recalled by Ethicon, Inc. Due to The...

The Issue: The needle associated with certain suture product codes has the potential to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2018· Roche Diabetes Care, Inc.

Recalled Item: Accu-Chek Inform II Test Strip Recalled by Roche Diabetes Care, Inc. Due to...

The Issue: The recalling firm has identified two lots of test strips that are out of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2018· Ethicon, Inc.

Recalled Item: PRONOVA SUTURE BLUE 122CM M1.5 Recalled by Ethicon, Inc. Due to The needle...

The Issue: The needle associated with certain suture product codes has the potential to...

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

Class II — Potential Health HazardOngoing