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. 2,630 recalls have been distributed to Georgia in the last 12 months.
Showing 33841–33860 of 53,623 recalls
Recalled Item: Unna-Z Recalled by Medline Industries Inc Due to Medline Industries, Inc is...
The Issue: Medline Industries, Inc is recalling Unna Z Unna Boot Bandage 3 X10 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NucliSENS magnetic extraction reagents Recalled by BioMerieux SA Due to A...
The Issue: A drift of the performance with the BK test (BK virus, worst case...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MagSIL (NucliSENS easyMAG Magnetic Silica) Recalled by BioMerieux SA Due to...
The Issue: A drift of the performance with the BK test (BK virus, worst case...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Straumann Drill 1 Recalled by Straumann Manufacturing, Inc. Due to Drills...
The Issue: Drills cannot be inserted into handpiece due to tolerance specification not met
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Straumann Twist Drill PRO ¿4.2mm Recalled by Straumann Manufacturing, Inc....
The Issue: Drills cannot be inserted into handpiece due to tolerance specification not met
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROTONIX I.V. (pantoprazole sodium) for Injection Recalled by Pfizer Inc....
The Issue: Subpotent Drug: Out of Specification (OOS) for potency at the 6-month...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Toms of Maine Naturally Dry Natural Powder Antiperspirant Stick Recalled by...
The Issue: Labeling: Label Mix Up- Incorrect back label applied to the product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Plush Puffs Marshmallows Toasty Coconut 4oz. and 2lb bulk bag Recalled by To...
The Issue: Undeclared allergen of milk from the declared ingredient coconut cream powder.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Durex Pleasure Pack . 3 ultra fine lubricated latex condoms Recalled by...
The Issue: Reckitt Benckiser LLC is recalling Durex Condoms Pleasure Packs due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Scope Power Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Siemens is providing a new installation of the Residual Current Monitor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ceres-C Standalone Cervical Interbody The product is a stand-alone anterior...
The Issue: Absent tantalum market pin.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIEMENS IMMULITE 2000/2000 Xpi Systems Intact PTH (Parathyroid Hormone) Test...
The Issue: Siemens is conducting this recall for the IMMULITE¿ 2000/IMMULITE¿ 2000 XPi...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: G3 Opticage Expandable Interbody Fusion Device Recalled by Interventional...
The Issue: During implantation, the proximal end of the device could separate if the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Perspective Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Siemens is providing a new installation of the Residual Current Monitor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Scope Recalled by Siemens Medical Solutions USA, Inc Due to Siemens...
The Issue: Siemens is providing a new installation of the Residual Current Monitor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K-Wire 1.4mm x 12in Non-Threaded Recalled by Amendia, Inc Due to The rods...
The Issue: The rods are packaged in packages with unacceptable seals. In some cases,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Black Widow 6.6mm x 20mm Screw Recalled by Amendia, Inc Due to There is a...
The Issue: There is a problem with the mating feature between the plate and screw which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zeus-P Lumbar Interbody Device Recalled by Amendia, Inc Due to Labeling...
The Issue: Labeling error where three boxes in inventory had conflicting patient and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dual Stylet Needle Recalled by Amendia, Inc Due to The rods are packaged in...
The Issue: The rods are packaged in packages with unacceptable seals. In some cases,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optimus Fixed Awl Recalled by Amendia, Inc Due to Complaints that the tip of...
The Issue: Complaints that the tip of the awl broke after impaction during surgery.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.