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. 2,549 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
2,549 in last 12 months

Showing 5284152860 of 53,623 recalls

FoodMay 17, 2012· International Flavors & Fragrances, Inc

Recalled Item: Grilled Chicken Marinade Recalled by International Flavors & Fragrances, Inc...

The Issue: Product has the potential to be contaminated with Salmonella.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodMay 17, 2012· International Flavors & Fragrances, Inc

Recalled Item: Nat Beef FF Recalled by International Flavors & Fragrances, Inc Due to...

The Issue: Product has the potential to be contaminated with Salmonella.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 17, 2012· Stryker Medical Division of Stryker Corporation

Recalled Item: GoBed+ . Model FL20E Beds are intended for medical purposes Recalled by...

The Issue: An adverse trend of scale and bed exit service reports/complaints were...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2012· Stryker Medical Division of Stryker Corporation

Recalled Item: Stryker Rose Bed Model (FL14E) Beds are intended for medical Recalled by...

The Issue: An adverse trend of scale and bed exit service reports/complaints were...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2012· Stryker Medical Division of Stryker Corporation

Recalled Item: Stryker MA204 Bed Model (FL25E) Beds are intended for medical Recalled by...

The Issue: An adverse trend of scale and bed exit service reports/complaints were...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2012· Stryker Medical Division of Stryker Corporation

Recalled Item: Go Bed II+ Model FL28C Beds are intended for medical Recalled by Stryker...

The Issue: An adverse trend of scale and bed exit service reports/complaints were...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2012· Stryker Medical Division of Stryker Corporation

Recalled Item: Go Bed II+ Model FL 28 Ex Beds are intended Recalled by Stryker Medical...

The Issue: An adverse trend of scale and bed exit service reports/complaints were...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2012· DePuy Orthopaedics, Inc.

Recalled Item: LUSTER HIP SZ 2 Packaging: The product was packaged within Recalled by DePuy...

The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2012· DePuy Orthopaedics, Inc.

Recalled Item: LUSTER HIP SZ 1 Packaging: The product was packaged within Recalled by DePuy...

The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2012· DePuy Orthopaedics, Inc.

Recalled Item: LUSTER HIP SZ 3 Packaging: The product was packaged within Recalled by DePuy...

The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2012· DePuy Orthopaedics, Inc.

Recalled Item: LUSTER HIP SZ 9 Packaging: The product was packaged within Recalled by DePuy...

The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2012· DePuy Orthopaedics, Inc.

Recalled Item: ULTIMA*LX STM Recalled by DePuy Orthopaedics, Inc. Due to DePuy...

The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2012· DePuy Orthopaedics, Inc.

Recalled Item: LUSTER HIP SZ 5 Packaging: The product was packaged within Recalled by DePuy...

The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2012· DePuy Orthopaedics, Inc.

Recalled Item: ULTIMA*LX STM Recalled by DePuy Orthopaedics, Inc. Due to DePuy...

The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2012· DePuy Orthopaedics, Inc.

Recalled Item: ULTIMA*LX STM Recalled by DePuy Orthopaedics, Inc. Due to DePuy...

The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2012· DePuy Orthopaedics, Inc.

Recalled Item: ULTIMA*LX STM Recalled by DePuy Orthopaedics, Inc. Due to DePuy...

The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2012· DePuy Orthopaedics, Inc.

Recalled Item: LUSTER HIP SZ 10 Packaging: The product was packaged within Recalled by...

The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2012· DePuy Orthopaedics, Inc.

Recalled Item: ULTIMA*LX STM Recalled by DePuy Orthopaedics, Inc. Due to DePuy...

The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2012· DePuy Orthopaedics, Inc.

Recalled Item: LUSTER HIP SZ 6 Packaging: The product was packaged within Recalled by DePuy...

The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2012· DePuy Orthopaedics, Inc.

Recalled Item: LUSTER HIP SZ 7 Packaging: The product was packaged within Recalled by DePuy...

The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER...

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

Class II — Potential Health HazardOngoing