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. 2,622 recalls have been distributed to Florida in the last 12 months.
Showing 43781–43800 of 55,837 recalls
Recalled Item: Medical Device Exchange Surgical Gown - Flyte Hood Pouch 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: Medical Device Exchange - Dilating Tip Trocar w/Stability Sleeve 11mm...
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: Medical Device Exchange -APPLIER 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: 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: 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: Medical Device Exchange FEMORAL CANAL TIP Recalled by EXP Pharmaceutical...
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: Medical Device Exchange PhysioMesh Flexible Composite Mesh 10cm x 15cm...
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: 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: 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: 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: 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: 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: Dextroamphetamine Sulfate Extended-Release Capsules Recalled by Actavis...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or 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 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: 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: 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: Antacid Liquid Regular Strength Antacid & Anti-Gas (Aluminum hydroxide 200...
The Issue: Microbial Contamination of Non-Sterile Products: Lots failed microbiological...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: See's Candies Classic Red Heart with Assorted Chocolates (8 oz. 227 g)...
The Issue: One packaging run of 8 oz. Classic Red Hearts with Assorted Chocolates was...
Recommended Action: Do not consume. Return to store for a refund or discard.