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. 2,866 recalls have been distributed to Florida in the last 12 months.
Showing 13541–13560 of 55,837 recalls
Recalled Item: Effluent Sample Bag Recalled by Baxter Healthcare Corporation Due to Certain...
The Issue: Certain Peritoneal Dialysis product codes do not have FDA regulatory...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Yes! Enoki Mushrooms Recalled by T Fresh Company DBA Yes Produce Due to...
The Issue: California Department of Public Health sampled product with a result of...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Olympus URETERO-RENO FIBERSCOPE Model: URF-P6R Recalled by Olympus...
The Issue: Incorrect adhesive used to secure the diopter ring and nameplate ring....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus URETERO-RENO FIBERSCOPE Model: URF-P6 Recalled by Olympus...
The Issue: Incorrect adhesive used to secure the diopter ring and nameplate ring....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus CYSTONEPHROFIBERSCOPE Model: CYF-5 Recalled by Olympus Corporation...
The Issue: Incorrect adhesive used to secure the diopter ring and nameplate ring....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proteus235- Proton Therapy System: to produce and deliver a proton Recalled...
The Issue: First layer of Uniform Scanning treatment fields is sometimes irradiated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The C304-HIS device features a guide wire to access the vein Recalled by...
The Issue: The firm's internal processes identified that certain lots may have an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardioblate" Gemini"-s Irrigated RF Surgical Ablation System Recalled by...
The Issue: Firm detected an increase in complaints related to fractured jaw tips of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WHOLE FOODS MARKET red lentil dal NET WT. 12 OZ Recalled by Bakkavor Foods...
The Issue: Possible Listeria monocytogenes in product
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Product Name: TEG5000 Analyzer (07-022 Recalled by Haemonetics Corporation...
The Issue: When the TEG 5000 Analyzer including TEG Analytical Software is used with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEGION NARROW PS OXIN SZ 6N RT and JRNY II BCS FEMORAL OXIN LT SZ 5 Recalled...
The Issue: It was reported that a JOURNEY II BCS Femoral OXIN LT SZ5 was in a box...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 'KORICA' ROASTED PEANUT Recalled by Rong Shing Trading NY Inc Due to Product...
The Issue: Product contains cyclamate, an unapproved color.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Medfusion Syringe Pump Models: 3500 Recalled by Smiths Medical ASD Inc. Due...
The Issue: Multiple issues with the potential for interruption of therapy or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medfusion Syringe Pump Model: Model 4000-0100-50 Recalled by Smiths Medical...
The Issue: Multiple issues with the potential for interruption of therapy or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Replacement back up batteries distributed on or after April 1 Recalled by GE...
The Issue: Insufficient battery backup power resulting in premature shutdown of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Back up batteries in Ventilators labeled as the following: a. Recalled by GE...
The Issue: Insufficient battery backup power resulting in premature shutdown of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: progenamatrix Human Keratin Matrix Recalled by ProgenaCare Due to Inner...
The Issue: Inner pouch seal may be inadequate resulting in lack of sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProterixBio SARS-CoV-2 (RBD) IgG Antibody Test Recalled by PROTERIXBIO Due...
The Issue: FDA review concluded that the test is insufficiently supported by clinical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Losartan Potassium Tablets Recalled by Macleods Pharma Usa Inc Due to CGMP...
The Issue: CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan Potassium Tablets Recalled by Macleods Pharma Usa Inc Due to CGMP...
The Issue: CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.