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. 2,766 recalls have been distributed to Georgia in the last 12 months.
Showing 14621–14640 of 29,505 recalls
Recalled Item: V-TEK" Recalled by Zimmer GmbH Due to An investigation identified that the...
The Issue: An investigation identified that the products were possibly manufactured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drill for 2.7mm screw Recalled by Zimmer GmbH Due to An investigation...
The Issue: An investigation identified that the products were possibly manufactured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drill for 2.7mm screw Recalled by Zimmer GmbH Due to An investigation...
The Issue: An investigation identified that the products were possibly manufactured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drill for 3.5mm screw Recalled by Zimmer GmbH Due to An investigation...
The Issue: An investigation identified that the products were possibly manufactured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CBS 4.0 countersink Recalled by Zimmer GmbH Due to An investigation...
The Issue: An investigation identified that the products were possibly manufactured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drill Recalled by Zimmer GmbH Due to An investigation identified that the...
The Issue: An investigation identified that the products were possibly manufactured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drill Recalled by Zimmer GmbH Due to An investigation identified that the...
The Issue: An investigation identified that the products were possibly manufactured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drill Recalled by Zimmer GmbH Due to An investigation identified that the...
The Issue: An investigation identified that the products were possibly manufactured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drill Recalled by Zimmer GmbH Due to An investigation identified that the...
The Issue: An investigation identified that the products were possibly manufactured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MediPress pneumatic compression system Recalled by Compass Health Brands...
The Issue: Product design change did not receive proper premarket clearance and lacks a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MediPress pneumatic compression system Full Leg (Short)-Segmental Gradient...
The Issue: Product design change did not receive proper premarket clearance and lacks a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MediPress pneumatic compression system Full Leg (Medium)-Segmental Gradient...
The Issue: Product design change did not receive proper premarket clearance and lacks a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MediPress pneumatic compression system Full Leg (Long)-Segmental Gradient...
The Issue: Product design change did not receive proper premarket clearance and lacks a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MediPress pneumatic compression system Full Arm (Short)-Segmental Gradient...
The Issue: Product design change did not receive proper premarket clearance and lacks a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MediPress pneumatic compression system Full Arm (Medium)-Segmental Gradient...
The Issue: Product design change did not receive proper premarket clearance and lacks a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Concorde Lift Recalled by DePuy Spine, Inc. Due to A complaint trend was...
The Issue: A complaint trend was observed for post-operative loss of height and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Concorde Lift Recalled by DePuy Spine, Inc. Due to A complaint trend was...
The Issue: A complaint trend was observed for post-operative loss of height and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity i Processing Module Recalled by Abbott Gmbh & Co. KG Due to...
The Issue: Potential loose cable connections on the reagent cooler, which could result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SoundWave Professional Suite Software 3.2 Recalled by Advanced Bionics, LLC...
The Issue: The manufacturer received complaints that customers were attempting to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas p 501 post-analytical units Recalled by Roche Diagnostics Corporation...
The Issue: There is a potential for the tray input flap on the post analytical units to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.