Product Recalls in Florida
Product recalls affecting Florida — including food, drugs, consumer products, medical devices, and vehicles distributed to Florida. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,754 recalls have been distributed to Florida in the last 12 months.
Showing 20941–20960 of 55,837 recalls
Recalled Item: Pioglitazone and Metformin Hydrochloride Tablets Recalled by Macleods Pharma...
The Issue: Subpotent Drug: Out of specification assay result, below specification, for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: QUESOS LA RICURA brand Queso Cotija Recalled by Quesos La Ricura, Ltd. Due...
The Issue: Possible contamination with Shiga toxin-producing E. coli (STEC).
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: PREVI Isola Insrument and PREVI Isola Printer spares PSUs (power supply...
The Issue: The recall has been initiated due to potential for overheating or a fire...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
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: 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: Ellipse Recalled by St Jude Medical, Cardiac Rhythm Management Division Due...
The Issue: Past updates to programmers and transmitters may lead some implantable...
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: Sysmex CV-11 Sample Unit Recalled by Sysmex America, Inc. Due to When...
The Issue: When excessive amounts of urine spills on the rack transport track and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
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.