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. 1,122 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
1,122 in last 12 months

Showing 13841–13860 of 29,505 recalls

Medical DeviceJune 25, 2019· BioPro, Inc.

Recalled Item: Go-EZ Screw 6.5x90 Recalled by BioPro, Inc. Due to Manufacturing flaw in the...

The Issue: Manufacturing flaw in the sterile barrier system

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2019· BioPro, Inc.

Recalled Item: Go-EZ Screw 6.5x110 Recalled by BioPro, Inc. Due to Manufacturing flaw in...

The Issue: Manufacturing flaw in the sterile barrier system

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2019· BioPro, Inc.

Recalled Item: K-Wire Sterile Single Trochar .045 Recalled by BioPro, Inc. Due to...

The Issue: Manufacturing flaw in the sterile barrier system

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2019· BioPro, Inc.

Recalled Item: K-Wire HBS Sterile Recalled by BioPro, Inc. Due to Manufacturing flaw in the...

The Issue: Manufacturing flaw in the sterile barrier system

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2019· BioPro, Inc.

Recalled Item: Go-EZ Screw 6.5x30 Recalled by BioPro, Inc. Due to Manufacturing flaw in the...

The Issue: Manufacturing flaw in the sterile barrier system

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2019· BioPro, Inc.

Recalled Item: K-Wire Sterile Single Trochar Recalled by BioPro, Inc. Due to Manufacturing...

The Issue: Manufacturing flaw in the sterile barrier system

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2019· BioPro, Inc.

Recalled Item: Go-EZ Screw 6.5x100 Recalled by BioPro, Inc. Due to Manufacturing flaw in...

The Issue: Manufacturing flaw in the sterile barrier system

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2019· BioPro, Inc.

Recalled Item: Go-EZ Screw 6.5x38 Recalled by BioPro, Inc. Due to Manufacturing flaw in the...

The Issue: Manufacturing flaw in the sterile barrier system

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2019· BioPro, Inc.

Recalled Item: Go-EZ Screw 6.5x95 Recalled by BioPro, Inc. Due to Manufacturing flaw in the...

The Issue: Manufacturing flaw in the sterile barrier system

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2019· BioPro, Inc.

Recalled Item: K-Wire Single Trocar 2.5x170mm Recalled by BioPro, Inc. Due to Manufacturing...

The Issue: Manufacturing flaw in the sterile barrier system

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2019· BioPro, Inc.

Recalled Item: Go-EZ Screw 6.5x36 Recalled by BioPro, Inc. Due to Manufacturing flaw in the...

The Issue: Manufacturing flaw in the sterile barrier system

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2019· BioPro, Inc.

Recalled Item: Go-EZ Screw 6.5x32 Recalled by BioPro, Inc. Due to Manufacturing flaw in the...

The Issue: Manufacturing flaw in the sterile barrier system

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2019· BioPro, Inc.

Recalled Item: Go-EZ Screw 6.5x105 Recalled by BioPro, Inc. Due to Manufacturing flaw in...

The Issue: Manufacturing flaw in the sterile barrier system

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2019· BioPro, Inc.

Recalled Item: K-Wire Single Trocar 1.6x150mm Recalled by BioPro, Inc. Due to Manufacturing...

The Issue: Manufacturing flaw in the sterile barrier system

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2019· BioPro, Inc.

Recalled Item: K-Wire HBS Sterile Lot Recalled by BioPro, Inc. Due to Manufacturing flaw in...

The Issue: Manufacturing flaw in the sterile barrier system

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2019· BioPro, Inc.

Recalled Item: Go-EZ Screw 6.5x34 Recalled by BioPro, Inc. Due to Manufacturing flaw in the...

The Issue: Manufacturing flaw in the sterile barrier system

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2019· BioPro, Inc.

Recalled Item: K-Wire Single Trocar 1.1x150mm Recalled by BioPro, Inc. Due to Manufacturing...

The Issue: Manufacturing flaw in the sterile barrier system

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2019· BioPro, Inc.

Recalled Item: Go-EZ Screw 6.5x115 Recalled by BioPro, Inc. Due to Manufacturing flaw in...

The Issue: Manufacturing flaw in the sterile barrier system

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2019· BioPro, Inc.

Recalled Item: Go-EZ Screw 6.5x120 Recalled by BioPro, Inc. Due to Manufacturing flaw in...

The Issue: Manufacturing flaw in the sterile barrier system

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2019· Philips Medical Systems (Cleveland) Inc

Recalled Item: iCT SP Model # 728311 Recalled by Philips Medical Systems (Cleveland) Inc...

The Issue: In certain instances when performing a cardiac step and shoot acquisition...

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

Class II — Potential Health HazardOngoing