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. 2,939 recalls have been distributed to Florida in the last 12 months.
Showing 1941–1960 of 55,837 recalls
Recalled Item: Sukhi's CLASSIC CURRY PASTE Recalled by Jagpreet Enterprises, LLC. dba...
The Issue: Potential contamination with foreign objects (metal pieces).
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Medline Kits containing BD SureStep Foley Tray Systems: SKU/Description:...
The Issue: Kits contain SureStep Foley Tray Systems recalled by BD that include...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lorazepam Injection Recalled by Hikma Pharmaceuticals USA Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: An out-of-Specification for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LIFEPAK CR2 Part / Catalog Numbers / UDI-DI code: CR2-2-001451 Recalled by...
The Issue: Due to required inspections not being performed on products/units that have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIFEPAK 15 Part / Catalog Numbers / UDI-DI code: V15-7-000022 Recalled by...
The Issue: Due to required inspections not being performed on products/units that have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: X1 Model RXM1000 UDI Codes: (01)00860003983812(11)230504(21)X11001...
The Issue: Due to incorrect software configuration that potentially allows more than...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIFEPAK 1000 Part / Catalog Numbers / UDI-DI code: 320371500023 Recalled by...
The Issue: Due to required inspections not being performed on products/units that have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bartels ELISA Legionella Urinary Antigen. Model Number: B1029-440. In Vitro...
The Issue: Potential for Bartels ELISA Legionella Urinary Antigen kit B1029-440 lot 065...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amlodipine and Olmesartan Medoxomil Tablets Recalled by Ascend Laboratories,...
The Issue: Failed Dissolution Specifications: low dissolution results
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Belsomra (suvorexant) tablets Recalled by Merck & Co. Inc Due to Failed...
The Issue: Failed Dissolution Specifications: potential for delayed dissolution of the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Brand Name: CELSITE Product Name: CELSITE BABYPORT SET PUR 4 Recalled by...
The Issue: The potential for minor injury such as damage to the vessel and/or tearing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Battery Operated infusion pumps. t:slim X2 G5 Recalled by Tandem Diabetes...
The Issue: Insulin pumps manufactured with speakers from Revision A and B may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STA-Liquid Anti-Xa 4. Model/Catalog Number: 00311US. The STA - Liquid...
The Issue: Potential for contamination of STA-LIQUID ANTI-Xa by Stago Fibrinogen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STA Satellite. Product Code: All . All software versions. The Recalled by...
The Issue: Potential for contamination of STA-LIQUID ANTI-Xa by Stago Fibrinogen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STA-Liquid Anti-Xa 8. Model/Catalog Number: 00322US. The STA - Liquid...
The Issue: Potential for contamination of STA-LIQUID ANTI-Xa by Stago Fibrinogen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STA - Fibrinogen 5. Model/Catalog Number: 00674. The STA - Recalled by...
The Issue: Potential for contamination of STA-LIQUID ANTI-Xa by Stago Fibrinogen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Ultra IABP Catheter Kit Product Name: Ultra IABP Recalled by...
The Issue: Device contains indications for use and device compatibility claims that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Item #99273 chocolate Tres Leches Cheesecake Recalled by King Cheesecake...
The Issue: Pecans have the potential to be contaminated with Salmonella
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Item #2485 Assorted layer cake Recalled by King Cheesecake Company, Inc. Due...
The Issue: Pecans have the potential to be contaminated with Salmonella
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Item #1312 Carrot layer cake Recalled by King Cheesecake Company, Inc. Due...
The Issue: Pecans have the potential to be contaminated with Salmonella
Recommended Action: Do not consume. Return to store for a refund or discard.