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. 2,670 recalls have been distributed to Florida in the last 12 months.
Showing 39381–39400 of 55,837 recalls
Recalled Item: Zimmer Periarticular Locking Plate System 3.5mm Locking Screw 58 mm Length...
The Issue: Product on the package label did not match what was inside the package. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MOSAIQ Oncology Information System MOSAIQ is an oncology information system...
The Issue: Incorrect drug dosage due to "Age Limit" and patient weight data item issue.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SYNTHECEL Dura Repair Recalled by Synthes (USA) Products LLC Due to It was...
The Issue: It was reported that the SYNTHECEL Dura Repair could adhere to various...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SYNTHECEL Dura Repair Recalled by Synthes (USA) Products LLC Due to It was...
The Issue: It was reported that the SYNTHECEL Dura Repair could adhere to various...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SYNTHECEL Dura Repair Recalled by Synthes (USA) Products LLC Due to It was...
The Issue: It was reported that the SYNTHECEL Dura Repair could adhere to various...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SYNTHECEL Dura Repair Recalled by Synthes (USA) Products LLC Due to It was...
The Issue: It was reported that the SYNTHECEL Dura Repair could adhere to various...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SYNTHECEL Dura Repair Recalled by Synthes (USA) Products LLC Due to It was...
The Issue: It was reported that the SYNTHECEL Dura Repair could adhere to various...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AltiVate Reverse Humeral Broach Recalled by Encore Medical, Lp Due to The...
The Issue: The trial shell mating feature on the broach is undersized.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perkin Elmer WIZARD2 10-detector Recalled by Perkinelmer Due to The content...
The Issue: The content of the second #023 barcode ID label in the Barcode ID Label...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perkin Elmer WIZARD2 1-detector Recalled by Perkinelmer Due to The content...
The Issue: The content of the second #023 barcode ID label in the Barcode ID Label...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perkin Elmer WIZARD2 1-detector Recalled by Perkinelmer Due to The content...
The Issue: The content of the second #023 barcode ID label in the Barcode ID Label...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perkin Elmer WIZARD2 5-detector Recalled by Perkinelmer Due to The content...
The Issue: The content of the second #023 barcode ID label in the Barcode ID Label...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perkin Elmer WIZARD2 10-detector Recalled by Perkinelmer Due to The content...
The Issue: The content of the second #023 barcode ID label in the Barcode ID Label...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perkin Elmer WIZARD2 2-detector Recalled by Perkinelmer Due to The content...
The Issue: The content of the second #023 barcode ID label in the Barcode ID Label...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perkin Elmer ClWIZARD2 5-detector Recalled by Perkinelmer Due to The content...
The Issue: The content of the second #023 barcode ID label in the Barcode ID Label...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quinapril Tablets USP 5 mg Recalled by Lupin Pharmaceuticals Inc. Due to...
The Issue: Failed Impurities/Degradation Specifications; Impurity A
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pioneer Sweet Corn Muffin Mix NET WT. 5 LBS 2.27 kg Recalled by C. H....
The Issue: May contain small metal fragments from wire mesh sifter.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: HSRG Cornmeal Breader NET WT 25 LB (11.33 kg) Recalled by C. H. Guenther &...
The Issue: May contain small metal fragments from wire mesh sifter.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Morrison's Pancake Mix Net Wt 5 LB (2.27 kg) Recalled by C. H. Guenther &...
The Issue: May contain small metal fragments from wire mesh sifter.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: HEB Lemon Seasonal Fish Fry Mix NET WT. 16 OZ Recalled by C. H. Guenther &...
The Issue: May contain small metal fragments from wire mesh sifter.
Recommended Action: Do not consume. Return to store for a refund or discard.