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. 2,686 recalls have been distributed to Georgia in the last 12 months.
Showing 20461–20480 of 53,623 recalls
Recalled Item: LN 3R70-01 Recalled by Abbott Gmbh & Co. KG Due to Abbott has identified...
The Issue: Abbott has identified potential performance issues for the Alinity ci...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTIS Pheno-Interventional Fluoroscopic X-Ray System Model Number: 10849000...
The Issue: Potential exists for one or more axes of the robotic stand to become blocked...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kroger Unbleached All Purpose Enriched Flour Recalled by Ardent Mills LLC...
The Issue: Product may be contaminated with Salmonella.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: DABRA Laser (RA-308 Excimer Laser). The DABRA Laser and DABRA Recalled by Ra...
The Issue: A software issue was identified which could result in user or patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Minocycline Hydrochloride Extended-Release Tablets Recalled by Ascend...
The Issue: Failed Dissolution Specifications: low out of specification results for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Triton Canister System (finished part numbers FG 12009 Recalled by Stryker...
The Issue: Some Canister Scanning Labels used to calibrate the Triton Canister System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FilmArray BCID Panel Recalled by BioFire Diagnostics, LLC Due to There is an...
The Issue: There is an increased risk of false positive Proteus results when using the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FilmArray BCID Panel Recalled by BioFire Diagnostics, LLC Due to There is an...
The Issue: There is an increased risk of false positive Proteus results when using the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Braemar Manufacturing LLC DL950 Holter Monitor 1285 Corporate Center Dr....
The Issue: An issue with the DL900 and DL950 Series Holter Recorder was recognized on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Braemar Manufacturing LLC DL900 Holter Monitor 1285 Corporate Center Dr....
The Issue: An issue with the DL900 and DL950 Series Holter Recorder was recognized on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: All Dietary Supplement manufactured and distributed by ABH Nature's Products...
The Issue: Firm ordered by consent decree to recall all products because the products...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Columbus R/PS TIB.PLATEAU Cemented Recalled by Aesculap Implant Systems LLC...
The Issue: Low Density Polyethylene (LDPE) particles may be present on the surface of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COLUMBUS CRA/PSA TIB.PLAT.CEMENTED Recalled by Aesculap Implant Systems LLC...
The Issue: Low Density Polyethylene (LDPE) particles may be present on the surface of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COLUMBUS CR/PS TIB.PLAT.PLASMAPORE Recalled by Aesculap Implant Systems LLC...
The Issue: Low Density Polyethylene (LDPE) particles may be present on the surface of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AS COLUMBUS CR/PS TIB.PLAT.CEMENTED Recalled by Aesculap Implant Systems LLC...
The Issue: Low Density Polyethylene (LDPE) particles may be present on the surface of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COLUMBUS REV F TIBIA OFFSET CEMENTED Recalled by Aesculap Implant Systems...
The Issue: Low Density Polyethylene (LDPE) particles may be present on the surface of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PTS Detect Cotinine Recalled by Polymer Technology Systems, Inc. Due to The...
The Issue: The firm is removing the product from the market after discussions with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Selenia Dimensions Mammography System Recalled by Hologic, Inc. Due to The...
The Issue: The recalling firm has received reports from the field of the C-arm on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Montelukast Sodium Chewable Tablets Recalled by Macleods Pharma Usa Inc Due...
The Issue: Failed Dissolution Specifications: testing revealed low out of specification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Econocare Plus Overlay Item: 1025EC. Intended to aid in the Recalled by...
The Issue: Due to a nonconformance of product contamination (human blood) of Econocare...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.