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. 2,710 recalls have been distributed to Florida in the last 12 months.
Showing 26441–26460 of 55,837 recalls
Recalled Item: Clozapine Orally Disintegrating Tablets Recalled by Teva Pharmaceuticals USA...
The Issue: Failed Disintegration Specifications: Out-of-specification disintegration...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nystatin and Triamcinolone Acetonide Cream Recalled by Dr. Reddy's...
The Issue: Failed stability specifications - An out of specification result was...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Glipizide XL (glipizide) extended-release tablets 5 mg 500-tablet bottle...
The Issue: CGMP Deviations; rejected product was used to manufacture final bulk lot
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Meropenem for Injection Recalled by Pfizer Inc. Due to Lack of assurance of...
The Issue: Lack of assurance of sterility: loss of container integrity.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Formed Hash Brown Patties Recalled by Lamb Weston Inc Due to Hash brown...
The Issue: Hash brown product, sold under brands Brookshire's, Market Pantry,...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Murry's Hash Brown Potato Patties Recalled by Lamb Weston Inc Due to Hash...
The Issue: Hash brown product, sold under brand Murry's is recalled because the product...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Single-Use Biopsy Forceps Recalled by Micro-Tech (Nanjing) Co., Ltd. Due to...
The Issue: Single-Use Biopsy Forceps box contains incorrect product, instead it...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Hybrid IABP Recalled by Maquet Datascope Corp - Cardiac Assist...
The Issue: There is a potential for interruption and/or inability to start therapy to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AS-OBGYN Information System version 7.824.x Recalled by AS Software, Inc....
The Issue: Any change made to current ultrasound machine software or hardware upgrades,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Rescue IABP Recalled by Maquet Datascope Corp - Cardiac Assist...
The Issue: There is a potential for interruption and/or inability to start therapy to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips DigitalDiagnost software 4.1.x and 4.2.x Recalled by Philips Medical...
The Issue: Stitching run on SkyPlate detector interrupted intermittently; Stitching...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elelyso (taliglucerase alfa) for injection Recalled by Pfizer Inc. Due to...
The Issue: Lack of assurance of sterility -Reports of loose metal ferrule crimps on...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bumetanide Tablets Recalled by Upsher Smith Laboratories, Inc. Due to Failed...
The Issue: Failed impurities/ degradation specifications: Product is Out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bumetanide Tablets Recalled by Upsher Smith Laboratories, Inc. Due to Failed...
The Issue: Failed impurities/ degradation specifications: Product is Out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Altavera Levonorgestrel and Ethinyl Estradiol Tablets Recalled by Xiromed...
The Issue: Labeling: Not Elsewhere Classified: mislabeling of the Altavera generic name...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Puritan Bennett 980 (PB980) ventilator series: Puritan Bennett" 980...
The Issue: Software Update: External USB Drive performance and its impact on Graphic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Access Cortisol Reagent. REF (Catalog Number) 33600 Recalled by Beckman...
The Issue: Cross contamination may have occurred between wells for the reagent pack. As...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Purus Labs MYOWHEY Premium Whey Protein Recalled by Purus Labs, Inc. Due to...
The Issue: Undeclared milk and soy.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Medtronic Navigation 0-arm 02 Imaging System interventional fluoroscopic...
The Issue: O-arm 02 Imaging Systems correction to software version 4.1.0; new version...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NucliSENS¿ Magnetic Extraction Reagents Recalled by BioMerieux SA Due to...
The Issue: Data loggers showed that one shipment to the United States experienced low...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.