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. 1,922 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
1,922 in last 12 months

Showing 2920129220 of 53,623 recalls

FoodDecember 12, 2017· Rachael's Food Corporation

Recalled Item: Rachael's SPRINGFIELD SMOKED FISH STRAWBERRY CREAM CHEESE SPREAD Recalled by...

The Issue: Product may be contaminated with Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 12, 2017· Rachael's Food Corporation

Recalled Item: SPRINGFIELD SMOKED FISH Smoked Sable Recalled by Rachael's Food Corporation...

The Issue: Product may be contaminated with Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 12, 2017· Rachael's Food Corporation

Recalled Item: SPRINGFIELD SMOKED Whitefish Meat Recalled by Rachael's Food Corporation Due...

The Issue: Product may be contaminated with Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 12, 2017· Rachael's Food Corporation

Recalled Item: SPRINGFIELD SMOKED FISH CHUNKY WHITEFISH SPREAD 8 oz. Recalled by Rachael's...

The Issue: Product may be contaminated with Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 12, 2017· Rachael's Food Corporation

Recalled Item: SPRINGFIELD SMOKED FISH Smoked Whole Whitefish Recalled by Rachael's Food...

The Issue: Product may be contaminated with Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 12, 2017· Rachael's Food Corporation

Recalled Item: SPRINGFIELD SMOKED FISH Smoked Chubs Recalled by Rachael's Food Corporation...

The Issue: Product may be contaminated with Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 12, 2017· Keryx Biopharmaceuticals, Inc.

Recalled Item: Auryxia (ferric citrate) tablets Recalled by Keryx Biopharmaceuticals, Inc....

The Issue: Presence of Foreign Substance: Reports have been received of damaged...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
Medical DeviceDecember 12, 2017· Boston Scientific Corporation

Recalled Item: Malecot Nephrostomy Catheter System Recalled by Boston Scientific...

The Issue: Certain Malecot Nephrostomy Catheters are breaking at the mid-shaft bond...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2017· Boston Scientific Corporation

Recalled Item: Re-Entry" Malecot Nephrostomy Catheter Set Recalled by Boston Scientific...

The Issue: Certain Malecot Nephrostomy Catheters are breaking at the mid-shaft bond...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2017· Boston Scientific Corporation

Recalled Item: Re-Entry" Malecot Nephrostomy Catheter Set Recalled by Boston Scientific...

The Issue: Certain Malecot Nephrostomy Catheters are breaking at the mid-shaft bond...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2017· Boston Scientific Corporation

Recalled Item: Percutaneous Access Set Recalled by Boston Scientific Corporation Due to...

The Issue: Certain Malecot Nephrostomy Catheters are breaking at the mid-shaft bond...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2017· Boston Scientific Corporation

Recalled Item: Malecot Nephrostomy Catheter Set Recalled by Boston Scientific Corporation...

The Issue: Certain Malecot Nephrostomy Catheters are breaking at the mid-shaft bond...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2017· Boston Scientific Corporation

Recalled Item: Malecot Nephrostomy Catheter Set Recalled by Boston Scientific Corporation...

The Issue: Certain Malecot Nephrostomy Catheters are breaking at the mid-shaft bond...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2017· Philips Electronics North America Corporation

Recalled Item: digital x-ray detector ProGrade R1 - solid state X ray Recalled by Philips...

The Issue: It the WiFi connection between the SkyPlate detector and HP transfer point...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2017· Boston Scientific Corporation

Recalled Item: Boston Scientific Guider Softip XF Guide Catheter Product Usage: Is Recalled...

The Issue: Potential polymer material degradation.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2017· Sanofi Genzyme

Recalled Item: Synvisc-One ¿ (hylan G-F 20) Recalled by Sanofi Genzyme Due to Contamination...

The Issue: Contamination with Methylbacterium thiocyanatum

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2017· Smith & Nephew, Inc.

Recalled Item: smith&nephew Mini-Fragment Plating System Recalled by Smith & Nephew, Inc....

The Issue: Devices, incorrectly labeled as a VLP MINI-MOD 2.0MM STRAIGHT PLATE 8 HOLE,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2017· Smith & Nephew, Inc.

Recalled Item: smith&nephew Mini-Fragment Plating System Recalled by Smith & Nephew, Inc....

The Issue: Devices, incorrectly labeled as a VLP MINI-MOD 2.0MM STRAIGHT PLATE 8 HOLE,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2017· Remel Inc

Recalled Item: Remel Shigella sonnei Phase 1 & 2 Agglutinating Serum Recalled by Remel Inc...

The Issue: The serum may fail to agglutinate within the specified minimum reaction time.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2017· Zimmer Biomet, Inc.

Recalled Item: Humeral Stem 55mm(Size 13) Product Usage: Intended for primary and Recalled...

The Issue: Zimmer Biomet is conducting a medical device recall for two lots of...

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

Class II — Potential Health HazardOngoing