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. 2,768 recalls have been distributed to Florida in the last 12 months.
Showing 18561–18580 of 30,686 recalls
Recalled Item: 108" 20 Drop Blood Set w/200 Micron Filter Recalled by ICU Medical, Inc. Due...
The Issue: Some devices were labeled as Does not contain DEHP even though the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 139" (353 cm) Y-Type Blood Set w/ 170 Micron Filter Recalled by ICU Medical,...
The Issue: Some devices were labeled as Does not contain DEHP even though the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 164" (417 cm) 20 Drop Y-Type Blood Admin Set w/200 Micron Filter Recalled by...
The Issue: Some devices were labeled as Does not contain DEHP even though the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cobas 8000 Modular Series system Recalled by Roche Diagnostics Corporation...
The Issue: A software failure may incorrectly set the system settings to "default"...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Convertors Robotic Drape with Attached Leggings Recalled by Cardinal Health...
The Issue: Product 29474 LAVH drape was packaged as 29574 Robotic Drape with Leggings.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rezum System Recalled by NXTHERA Due to Needle Bond may not be able to...
The Issue: Needle Bond may not be able to withstand the tension force applied when the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Magic 3 Antibacterial Hydrophilic Intermittent Catheter Female Recalled...
The Issue: Specific lots labeled as an Antibacterial Hydrophilic Intermittent Catheter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AIRO Mobile CT System Recalled by Brainlab AG Due to Risk of unintended...
The Issue: Risk of unintended motion while the AIRO system is in transport mode.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iVue with Normative Database Recalled by Optovue, Inc. Due to FDA determined...
The Issue: FDA determined that a 510(k) is needed for the Vault Mapping software (also...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A.T.S. 4000TS Tourniquet Systems Recalled by Zimmer Surgical Inc Due to...
The Issue: Updated on-device label and 3 pages of an updated Operator/Service Manual....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iFusion Recalled by Optovue, Inc. Due to FDA determined that a 510(k) is...
The Issue: FDA determined that a 510(k) is needed for the Vault Mapping software (also...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VCLAS (Visualase Cooled Laser Ablation System) Part Number: 9735559...
The Issue: The VCLAS 3mm, 10mm, and 15mm tip devices were not appropriately tested for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A.T.S. 2200TS Tourniquet Systems Recalled by Zimmer Surgical Inc Due to...
The Issue: Updated on-device label and 3 pages of an updated Operator/Service Manual....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iVue 500 with iScan Recalled by Optovue, Inc. Due to FDA determined that a...
The Issue: FDA determined that a 510(k) is needed for the Vault Mapping software (also...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Cardiopulmonary Bypass Custom Tubing kit BO-TOP 38600 ADULT CPB...
The Issue: There is a potential for the over-pressure safety (OPS) valve in the tubing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Cardiopulmonary Bypass Custom Tubing kit BEQ-T 4906 PEDIARIC CPB PACK...
The Issue: There is a potential for the over-pressure safety (OPS) valve in the tubing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Cardiopulmonary Bypass Custom Tubing kit BO-TOP 38600 ADULT CPB...
The Issue: There is a potential for the over-pressure safety (OPS) valve in the tubing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 9x15" Medium Utility Positioner with Cover Recalled by Molnlycke Health...
The Issue: Products may not meet specifications due to possible presence of metal shavings.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Concorde Lift Torque Limiting Handle. Must be used with supplemental...
The Issue: Potential for Intra-operative breakage of driver tips
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.5 mm Reaming Rod Recalled by Synthes (USA) Products LLC Due to Possible...
The Issue: Possible lack of product sterility due to potential gaps/channeling in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.