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. 2,786 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
2,786 in last 12 months

Showing 1186111880 of 29,505 recalls

Medical DeviceJune 4, 2020· Boston Scientific Corporation

Recalled Item: Ablation Galil Technology Recalled by Boston Scientific Corporation Due to...

The Issue: The needle surface deteriorated due to unexpected electrolysis during procedure.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2020· Boston Scientific Corporation

Recalled Item: Ablation Galil Technology Recalled by Boston Scientific Corporation Due to...

The Issue: The needle surface deteriorated due to unexpected electrolysis during procedure.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2020· Boston Scientific Corporation

Recalled Item: Ablation Galil Technology Recalled by Boston Scientific Corporation Due to...

The Issue: The needle surface deteriorated due to unexpected electrolysis during procedure.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2020· Boston Scientific Corporation

Recalled Item: Ablation Galil Technology Recalled by Boston Scientific Corporation Due to...

The Issue: The needle surface deteriorated due to unexpected electrolysis during procedure.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2020· Boston Scientific Corporation

Recalled Item: Ablation Galil Technology Recalled by Boston Scientific Corporation Due to...

The Issue: The needle surface deteriorated due to unexpected electrolysis during procedure.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2020· HF Acquisition Co., LLC

Recalled Item: HealthFirst Emergency Medical Kit Recalled by HF Acquisition Co., LLC Due to...

The Issue: Instead of 2 doses, packaged 1 dose of nasal spray in an emergency kits.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2020· Boston Scientific Corporation

Recalled Item: Ablation Galil Technology Recalled by Boston Scientific Corporation Due to...

The Issue: The needle surface deteriorated due to unexpected electrolysis during procedure.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2020· Boston Scientific Corporation

Recalled Item: Ablation Galil Technology Recalled by Boston Scientific Corporation Due to...

The Issue: The needle surface deteriorated due to unexpected electrolysis during procedure.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2020· Boston Scientific Corporation

Recalled Item: Ablation Galil Technology Recalled by Boston Scientific Corporation Due to...

The Issue: The needle surface deteriorated due to unexpected electrolysis during procedure.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2020· Boston Scientific Corporation

Recalled Item: Ablation Galil Technology Recalled by Boston Scientific Corporation Due to...

The Issue: The needle surface deteriorated due to unexpected electrolysis during procedure.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2020· HF Acquisition Co., LLC

Recalled Item: STAT KIT Model 550AI Emergency Medical Kit. P/N: 1010830 containing Recalled...

The Issue: Instead of 2 doses, packaged 1 dose of nasal spray in an emergency kits.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2020· LONGHORN VACCINES AND DIAGNOSTIC

Recalled Item: PrimeStore Molecular Transport Medium (PS-MTM) Recalled by LONGHORN VACCINES...

The Issue: The tubes may have been delivered to some users without labels. Users may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2020· CooperSurgical, Inc.

Recalled Item: COOPERSURGICAL Os FinderTM Cervical Dilator Recalled by CooperSurgical, Inc....

The Issue: Mislabeled: Printing on the top web or Tyvek lid of the individual product...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2020· Roche Molecular Systems, Inc.

Recalled Item: MagNA Pure 96 Instrument Recalled by Roche Molecular Systems, Inc. Due to...

The Issue: When using Sample Transfer protocol version 3.0, the drop catcher is not...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2020· Philips North America, LLC

Recalled Item: EasyDiagnost Eleva DRF Recalled by Philips North America, LLC Due to Thermo...

The Issue: Thermo switches in the main power supply for the system may be incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2020· Baxter Healthcare Corporation

Recalled Item: Flow Coupler Monitor Recalled by Baxter Healthcare Corporation Due to A...

The Issue: A firmware issue may cause the GEM1020M-2 Flow Coupler Monitor to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2020· TELEFLEX MEDICAL INC

Recalled Item: RUSCH LASERTUBE (Rubber) Recalled by TELEFLEX MEDICAL INC Due to Teleflex is...

The Issue: Teleflex is initiating a voluntary recall for the above-mentioned products...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2020· Carefusion 2200 Inc

Recalled Item: Safe-T-Centesis 8 Fr Catheter Drainage Tray Recalled by Carefusion 2200 Inc...

The Issue: The Universal Drainage Set (UDS) may contain valves that leak internally...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2020· Carefusion 2200 Inc

Recalled Item: Thora-Para 5 Fr Non-Valved Catheter Drainage Tray Recalled by Carefusion...

The Issue: The Universal Drainage Set (UDS) may contain valves that leak internally...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2020· Carefusion 2200 Inc

Recalled Item: Safe-T PLUS Thora-Para 8 Fr Catheter Drainage Tray Recalled by Carefusion...

The Issue: The Universal Drainage Set (UDS) may contain valves that leak internally...

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

Class II — Potential Health HazardOngoing