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. 2,793 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
2,793 in last 12 months

Showing 1176111780 of 53,623 recalls

Medical DeviceSeptember 9, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE ADLT BLOOD CLUTURE COLLECT KIT Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: Adult Blood Culture Collect kit and Pre-Op Changing Bathing Kit contain an...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 9, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE PHERIPHERAL BLOOD CULTURE DRAW Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: Adult Blood Culture Collect kit and Pre-Op Changing Bathing Kit contain an...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 9, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE PRE-OP CHG BATHING KIT Reorder #: P164756 Recalled by MEDLINE...

The Issue: Adult Blood Culture Collect kit and Pre-Op Changing Bathing Kit contain an...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 9, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE BLOOD CLUTURE KIT Recalled by MEDLINE INDUSTRIES, LP - Northfield...

The Issue: Adult Blood Culture Collect kit and Pre-Op Changing Bathing Kit contain an...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 9, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE 24 BLOOD CLUTURE KIT Recalled by MEDLINE INDUSTRIES, LP - Northfield...

The Issue: Adult Blood Culture Collect kit and Pre-Op Changing Bathing Kit contain an...

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

Class II — Potential Health HazardOngoing
FoodSeptember 8, 2022· Muktanand Foods Inc

Recalled Item: ANKUR Golden Raisin Recalled by Muktanand Foods Inc Due to Undeclared Sulfites

The Issue: Undeclared sulfites

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceSeptember 8, 2022· Abbott Vascular

Recalled Item: Product/Part: MitraClip XTR Clip Delivery System US/CDS0601-XTR Recalled by...

The Issue: An increase in clip locking malfunctions, Establish Final Arm Angle and Clip...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2022· Abbott Vascular

Recalled Item: Product/Part: MitraClip NTR Clip Delivery System US/CDS0601-NTR Recalled by...

The Issue: An increase in clip locking malfunctions, Establish Final Arm Angle and Clip...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2022· Abbott Vascular

Recalled Item: Product/Part: MitraClip G4 CDS NT REPAIR-MR Clinical/CDS0704-NT Recalled by...

The Issue: An increase in clip locking malfunctions, Establish Final Arm Angle and Clip...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2022· SunMed Holdings, LLC

Recalled Item: Full Kit Pulset 3cc Syringe 23g x 1 Safety Tip 25u BH Recalled by SunMed...

The Issue: The kits are being recalled due to a lack of sterility of a spare needle...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 7, 2022· Johnson & Johnson Surgical Vision, Inc.

Recalled Item: THERMOCOOL SMARTTOUCH SF Bi-Directional Navigation Catheter Recalled by...

The Issue: Manufacturing error resulted in potential contamination of Bi-Directional...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 7, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: CENTURION SnagFree Chest Tube insertion Tray Recalled by MEDLINE INDUSTRIES,...

The Issue: One lot of chest tube insertion trays, containing a silk suture component...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 7, 2022· BALT USA, LLC

Recalled Item: Optima Coil System Model Number OPTI0208CSS10 Recalled by BALT USA, LLC Due...

The Issue: Product pouch label does not match up with carton label

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 6, 2022· Philips Respironics, Inc.

Recalled Item: Wisp and Wisp Youth Nasal Mask Recalled by Philips Respironics, Inc. Due to...

The Issue: No contraindication/warning regarding magnetic components in CPAP masks for...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 6, 2022· Philips Respironics, Inc.

Recalled Item: DreamWisp Nasal Mask with Over the Nose Cushion Recalled by Philips...

The Issue: No contraindication/warning regarding magnetic components in CPAP masks for...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 6, 2022· Philips Respironics, Inc.

Recalled Item: Philips Respironics Amara View Minimal Contact Full-Face Mask Recalled by...

The Issue: No contraindication/warning regarding magnetic components in CPAP masks for...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 6, 2022· Philips North America Llc

Recalled Item: MR Patient Care Portal 5000 (Desktop Unit) Recalled by Philips North America...

The Issue: Device may intermittently fail to produce audio. Turning the unit off and on...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 6, 2022· Philips Respironics, Inc.

Recalled Item: Therapy Mask 3100 NC/SP Recalled by Philips Respironics, Inc. Due to No...

The Issue: No contraindication/warning regarding magnetic components in CPAP masks for...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 6, 2022· Philips Respironics, Inc.

Recalled Item: Philips Respironics DreamWear Full Face Mask Recalled by Philips...

The Issue: No contraindication/warning regarding magnetic components in CPAP masks for...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 2, 2022· LUMINOSTICS, INC dba CLIP HEALTH

Recalled Item: Clip COVID Rapid Antigen Test Kit (25-pack) Recalled by LUMINOSTICS, INC dba...

The Issue: COVID test kit shelf life was periodically extended, as real-time stability...

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

Class II — Potential Health HazardOngoing