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. 1,075 recalls have been distributed to Florida in the last 12 months.
Showing 17901–17920 of 55,837 recalls
Recalled Item: In2Bones Shannon Percutaneous Burr - Product Usage: indicated for forefoot...
The Issue: This Field Action is being conducted following identification of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Recalled by Philips North America LLC Due to Customers were not...
The Issue: Customers were not notified of previous recalls associated with various...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Recalled by Philips North America LLC Due to Customers were not...
The Issue: Customers were not notified of previous recalls associated with various...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Recalled by Philips North America LLC Due to Customers were not...
The Issue: Customers were not notified of previous recalls associated with various...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The ImmunoCard Mycoplasma EIA detects the presence of IgM to Recalled by...
The Issue: Use of the kits after incorrect storage could lead to a potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SHARP MEDICAL PRODUCTS Recalled by Sharp Medical Products Due to...
The Issue: Non-conformity (holes/punctures or deep creases) in the sterile barrier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mizuho CE IPX4 Recalled by Mizuho OSI Due to There is a potential that hand...
The Issue: There is a potential that hand control units may cause the tabletop to slide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Enzyme linked immunosorbent assay Recalled by Siemens Healthcare...
The Issue: Potential false positive HSV results. Siemens Healthcare Diagnostics, Inc....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NM/CT 850 Nuclear Medicine / CT Scanners Recalled by GE Healthcare, LLC Due...
The Issue: GE Healthcare has become aware of a potential issue on 800 family NM/CT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NM/CT 870 DR Nuclear Medicine / CT Scanners Recalled by GE Healthcare, LLC...
The Issue: GE Healthcare has become aware of a potential issue on 800 family NM/CT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NM/CT 860 Nuclear Medicine / CT Scanners Recalled by GE Healthcare, LLC Due...
The Issue: GE Healthcare has become aware of a potential issue on 800 family NM/CT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DJO EMPOWR KNEE Femoral Sizer Recalled by Encore Medical, LP Due to...
The Issue: Incorrect assembly of a subcomponent by a vendor and as a result, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: System INFX-8000F Recalled by Canon Medical System, USA, INC. Due to The...
The Issue: The x-ray irradiation field may shift with respect to image receiving...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: System INFX-8000V Recalled by Canon Medical System, USA, INC. Due to The...
The Issue: The x-ray irradiation field may shift with respect to image receiving...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: System INFX-8000C Recalled by Canon Medical System, USA, INC. Due to The...
The Issue: The x-ray irradiation field may shift with respect to image receiving...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Methamphetamine Intercept Microplate kit EIA - IVD qualitative determination...
The Issue: Incorrect lot of Substrate Reagent (TMB) may be included in the kit. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spicy Red Curry Sauce Recalled by Barbara's Orchard/Delicae Gourmet Due to...
The Issue: Undeclared allergen: Shrimp
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Panang Curry Sauce Recalled by Barbara's Orchard/Delicae Gourmet Due to...
The Issue: Undeclared allergen: Shrimp
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Thai Peanut Sauce Recalled by Barbara's Orchard/Delicae Gourmet Due to...
The Issue: Undeclared allergen: Shrimp
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Pantoprazole Sodium for Injection 40mg/vial For I.V. infusion only...
The Issue: Failed Impurity/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.