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. 2,785 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
2,785 in last 12 months

Showing 1368113700 of 29,505 recalls

Medical DeviceJuly 22, 2019· DeRoyal Industries Inc

Recalled Item: DeRoyal Enteral Safe Feeding Tubes: a) Recalled by DeRoyal Industries Inc...

The Issue: Certain MED-RX Polyurethane Feeding Tubes are being recalled due to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2019· Stryker Corporation

Recalled Item: Stryker Recalled by Stryker Corporation Due to Complaints have been received...

The Issue: Complaints have been received regarding difficulty in removing the driver...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2019· Stryker Corporation

Recalled Item: Stryker Recalled by Stryker Corporation Due to Complaints have been received...

The Issue: Complaints have been received regarding difficulty in removing the driver...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2019· Philips North America, LLC

Recalled Item: Philips 5-Lead Set Recalled by Philips North America, LLC Due to The...

The Issue: The thickness of the connector to the trunk cable on affected limb lead sets...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2019· Coltene /Whaledent AG

Recalled Item: DIATECH Recalled by Coltene /Whaledent AG Due to A single batch of Diatech...

The Issue: A single batch of Diatech Diamond dental burs, 856-016-7-F, Round end taper,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2019· Fujifilm Medical Systems U.S.A., Inc.

Recalled Item: Fujifilm FDR Go Plus mobile X-ray system Recalled by Fujifilm Medical...

The Issue: The graphics driver of the FDR Go PLUS might cause the appearance of a Blue...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2019· Cincinnati Sub-Zero Products LLC, a Gentherm Company

Recalled Item: MICRO-TEMP LT System Recalled by Cincinnati Sub-Zero Products LLC, a...

The Issue: Updated Manual-Warnigs have been added stating that exceeding 40'C for...

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

Class III — Low RiskOngoing
Medical DeviceJuly 18, 2019· Arrow International Inc

Recalled Item: Arrow AGB+ Multi-Lumen CVC Kit-catheter permits venous access to central...

The Issue: Arrow AGB+ Multi-Lumen CVC Kit - lidstock incorrectly states within...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2019· Medical Intelligence Medizintechnik Gmbh

Recalled Item: IGuide System Recalled by Medical Intelligence Medizintechnik Gmbh Due to...

The Issue: Sometimes, although the HexaPOD has reached the target position, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2019· Becton Dickinson & Co.

Recalled Item: Kit BD Max Enteric Viral Panel RUO Recalled by Becton Dickinson & Co. Due to...

The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2019· Becton Dickinson & Co.

Recalled Item: Kit BD Max StaphSR Recalled by Becton Dickinson & Co. Due to The foil bags...

The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2019· Becton Dickinson & Co.

Recalled Item: Kit BD Max ExK DNA 1 USA Recalled by Becton Dickinson & Co. Due to The foil...

The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2019· Becton Dickinson & Co.

Recalled Item: Kit EXT Enteric Bacterial Panel Recalled by Becton Dickinson & Co. Due to...

The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2019· Becton Dickinson & Co.

Recalled Item: Kit BD Max Check-Points CPO IVD EU Recalled by Becton Dickinson & Co. Due to...

The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2019· Becton Dickinson & Co.

Recalled Item: Kit BD Max Enteric Viral Panel EU Catalog # 443985 Recalled by Becton...

The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2019· Becton Dickinson & Co.

Recalled Item: Kit BD Max ExK TNA 2 Recalled by Becton Dickinson & Co. Due to The foil bags...

The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2019· Becton Dickinson & Co.

Recalled Item: Kit BD Max ExK DNA 1 EU LUO Recalled by Becton Dickinson & Co. Due to The...

The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2019· Becton Dickinson & Co.

Recalled Item: Kit BD Max MRSA Recalled by Becton Dickinson & Co. Due to The foil bags...

The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2019· Becton Dickinson & Co.

Recalled Item: Kit BD Max Vaginal Panel Recalled by Becton Dickinson & Co. Due to The foil...

The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2019· Becton Dickinson & Co.

Recalled Item: Kit BD Max ExK DNA 2 EU LUO Recalled by Becton Dickinson & Co. Due to The...

The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...

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

Class II — Potential Health HazardOngoing