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 1152111540 of 53,623 recalls

Medical DeviceNovember 1, 2022· Cardinal Health

Recalled Item: Dover Closed Urethral Tray with Vinyl Catheter Product Code: 3420 Recalled...

The Issue: Occlusion (blockage) of the bubble inlet port of the urinary drainage bag...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2022· Cardinal Health

Recalled Item: Dover Closed Urethral Tray with Vinyl Catheter 14 Fr/Ch (4.7 mm) Recalled by...

The Issue: Occlusion (blockage) of the bubble inlet port of the urinary drainage bag...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2022· Cardinal Health

Recalled Item: Dover Closed Urethral Tray with Hydrogel Coated Red Rubber Catheter Recalled...

The Issue: Occlusion (blockage) of the bubble inlet port of the urinary drainage bag...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2022· Alcon Research, LLC

Recalled Item: Alcon Custom Pak Surgical Procedure Pack Recalled by Alcon Research, LLC Due...

The Issue: Due to difficulty removing the liner on the adhesive components of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 28, 2022· GE Medical Systems, LLC

Recalled Item: Centricity Universal Viewer 6.0. Used to display medical images (Including...

The Issue: There is the potential that after installation of the IAS tool, some studies...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 28, 2022· GE Medical Systems, LLC

Recalled Item: Centricity PACS-IW with Universal Viewer version 5.0. Used to display...

The Issue: There is the potential that after installation of the IAS tool, some studies...

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

Class II — Potential Health HazardOngoing
FoodOctober 27, 2022· Taylor Farms Retail, Inc.

Recalled Item: BabyBel Snacker (FG0401 SW Snacker ACABB 5pk) Crunch Pak 5.75 Recalled by...

The Issue: Allergens of almonds and milk not declared on the product ingredient label

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 27, 2022· Rieckhoff Family Businesses, Inc dba Cedar Creek Popcorn

Recalled Item: Gourmet Old-Fashioned Caramel Holiday Popcorn Recalled by Rieckhoff Family...

The Issue: Label contains "Gluten Free" claim but product contains wheat and barley...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 27, 2022· ARROW INTERNATIONAL Inc.

Recalled Item: Pressure Injectable Arrowg+ard Blue Plus Three-Lumen CVC Kit Recalled by...

The Issue: There is the potential for inadequate connection between the top and bottom...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 27, 2022· ARROW INTERNATIONAL Inc.

Recalled Item: Arrow MAC Two-Lumen Central Venous Access Kit fr use with 7 - 7.5 Fr...

The Issue: There is the potential for inadequate connection between the top and bottom...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 27, 2022· Southmedic, Inc.

Recalled Item: Southmedic SAFETY CARTRIDGE WITH SOUTHMEDIC PLUS SURGICAL BLADE Recalled by...

The Issue: Upon review of its batch record, Southmedic identified that lot # W92761 was...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2022· Siemens Healthcare Diagnostics, Inc.

Recalled Item: IMMULITE and IMMULITE 1000 Total Testosterone Assay- In vitro diagnostic...

The Issue: Confirmed an average positive bias of 40% for testosterone concentrations of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2022· Trackx Technology Inc

Recalled Item: TrackX Insight Base Modular Instrument Tracker Recalled by Trackx Technology...

The Issue: The device is breaking and falling off the Nuvasive T-Handle with Hudson...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2022· Whele LLC DBA Perch

Recalled Item: Mighty Bliss Electric Heating Pad Recalled by Whele LLC DBA Perch Due to The...

The Issue: The products may have the potential to burn customers. Firm has received...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 24, 2022· Whele LLC DBA Perch

Recalled Item: Mighty Bliss Electric Heating Pad Recalled by Whele LLC DBA Perch Due to The...

The Issue: The products may have the potential to burn customers. Firm has received...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 24, 2022· Whele LLC DBA Perch

Recalled Item: Mighty Bliss Electric Heating Pad Recalled by Whele LLC DBA Perch Due to The...

The Issue: The products may have the potential to burn customers. Firm has received...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 24, 2022· Tollos

Recalled Item: Infection Control (IC) Lifting Strap used with the following Cirrus Recalled...

The Issue: Two customers reported four incidents in which the lifting strap broke while...

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

Class II — Potential Health HazardOngoing
DrugOctober 21, 2022· Viatris Inc

Recalled Item: Carvedilol Tablets Recalled by Viatris Inc Due to Failed Tablet/Capsule...

The Issue: Failed Tablet/Capsule Specifications: Tablets exceeds specification for...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 21, 2022· Philips North America Llc

Recalled Item: Philips ProxiDiagnost N90 1.0 (Model 706100) and ProxiDiagnost N90 1.1...

The Issue: Potential table stop due to a broken tabletop cable: On the ProxiDiagnost...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2022· Intersect ENT, Inc.

Recalled Item: Propel Mini Mometasone Furoate Sinus Implant Recalled by Intersect ENT, Inc....

The Issue: Sinus Implant product label displays incorrect product information...

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

Class II — Potential Health HazardOngoing