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. 2,723 recalls have been distributed to Florida in the last 12 months.
Showing 24621–24640 of 30,686 recalls
Recalled Item: EndoWrist One Vessel Sealer Recalled by Intuitive Surgical, Inc. Due to...
The Issue: Intuitive Surgical has identified the potential for a certain, small portion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical Device Exchange X-SAW BLADE Recalled by EXP Pharmaceutical Services...
The Issue: EXP did not register as a medical device establishment, list the devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Milestone Wand STA Handpiece for the delivery of local anesthesia Recalled...
The Issue: Wand Handpiece was mislabeled as STA handpiece. The Wand handpiece cannot be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoWrist One Vessel Sealer Recalled by Intuitive Surgical, Inc. Due to...
The Issue: Intuitive Surgical has identified the potential for a certain, small portion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SMARTSET GHV Gentamicin Bone Cement. A self-curing Recalled by DePuy...
The Issue: One lot of SMARTSET GHV Gentamicin Bone Cement is partially agglomerated ....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical Device Exchange BAG Recalled by EXP Pharmaceutical Services Corp Due...
The Issue: EXP did not register as a medical device establishment, list the devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Outer cardboard box labeling: Pinnacle Cure Sleeve Recalled by Sybron Dental...
The Issue: Cases of Cure Sleeve labeled with part number 4513, which fits 13mm tips,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical Device Exchange - GIA Auto Suture Loading Unit w/ Recalled by EXP...
The Issue: EXP did not register as a medical device establishment, list the devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: G7 Variant Elution Buffer HiS no. 1 (M) component of Recalled by Tosoh...
The Issue: The G7 Variant Elution Buffer HiS no. 1 (M) is incorrectly labeled with an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Healthcare DuraDiagnost X- Ray Recalled by Philips Medical Systems,...
The Issue: The system is designed to emit a beep upon termination of an exposure....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Healthcare DigitalDiagnost System X-Ray Recalled by Philips Medical...
The Issue: The system is designed to emit a beep upon termination of an exposure....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CooperSurgical PESSARY KIT-CUBE#2 Recalled by CooperSurgical, Inc. Due to...
The Issue: Incorrect size printed on the Milex Pessary Kit packaging label
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo HX2 Temperature Management System provides temperature control of two...
The Issue: Malfunctioning mixing valve and loss of cooling and/or heating capability....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIEMENS SOMATOM Force with software version VA50A and /or VA50A_FP1 Recalled...
The Issue: Possibility of image artifacts during data acquisition when using Adaptive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Computed Tomography X-ray Systems Ingenuity CT scanners. Intended to produce...
The Issue: 5 issues. Fast Get Ready incorrectly enabled during service procedures....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Computed Tomography X-ray systems Brilliance iCT Recalled by Philips Medical...
The Issue: 5 issues. Fast Get Ready incorrectly enabled during service procedures....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zip 8M Wound Closure Device Recalled by Zipline Medical Due to The...
The Issue: The manufacturers seal may not be present on the Nylon pouch resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Computed Tomography X-ray Systems Brilliance CT 64-channel with Essence...
The Issue: 5 issues. Fast Get Ready incorrectly enabled during service procedures....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARROW FiberOptix Intra-Aortic Balloon Catheter Kit Recalled by Arrow...
The Issue: Outer package product label incorrectly identifies the product as FiberOptix...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Computed Tomography X-ray Systems Ingenuity Core 128. Intended to produce...
The Issue: 5 issues. Fast Get Ready incorrectly enabled during service procedures....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.