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. 2,801 recalls have been distributed to Florida in the last 12 months.
Showing 18401–18420 of 55,837 recalls
Recalled Item: Roche cobas 8000 modular analyzer series (i.e. Recalled by Roche Diagnostics...
The Issue: Potential for Changed Configuration Settings on the cobas 8000 modular...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TraZODONE Hydrochloride Tablets USP 100 mg Recalled by AVKARE Inc. Due to...
The Issue: Product mix-up: Bottles of sildenafil and trazodone were inadvertently...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sildenafil Tablets USP 100 mg Recalled by AVKARE Inc. Due to Product mix-up:...
The Issue: Product mix-up: Bottles of sildenafil and trazodone were inadvertently...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sodium Chloride Injection Recalled by Hikma Pharmaceuticals USA Inc. Due to...
The Issue: Failed pH Specifications: Out of Specification pH Test Results were found in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Grace Medical *** COX BONE DUST COLLECTOR *** Recalled by Oto Med Inc Due to...
The Issue: During internal Age Testing, holes were found in the sterile Tyvek pouches...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Grace Medical *** spineX BONE DUST COLLECTOR *** Recalled by Oto Med Inc Due...
The Issue: During internal Age Testing, holes were found in the sterile Tyvek pouches...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Grace Medical *** SHEEHY BONE DUST COLLECTOR *** Recalled by Oto Med Inc Due...
The Issue: During internal Age Testing, holes were found in the sterile Tyvek pouches...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IOLMaster 700 Recalled by Carl Zeiss Meditec AG Due to When using software...
The Issue: When using software 1.90.2.09 or 1.90.8.06 and using modality worklist...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Holiday Cookie Platter packaged in plastic container 20 OZ (1.25 Recalled by...
The Issue: Undeclared pecans due to mis-labeling
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: visby medical COVID-19 Test kit *** An in vitro diagnostic Recalled by VISBY...
The Issue: Two issues: 1) 5 Lots were found to have incorrect labeling on the outer box...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lansoprazole Delayed-Release Orally Disintegrating Tablets 15 mg Recalled by...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lansoprazole Delayed-Release Orally Disintegrating Tablets Recalled by Zydus...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Stryker Medela .0193 AXS Universal Aspiration Tubing (01)07612367053921 -...
The Issue: Incorrect expiration date of "2023-07-24" on label of sterile tubing....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 60" (152 cm) Appx 1.9 ml Recalled by ICU Medical, Inc. Due to Due to the...
The Issue: Due to the incorrect filter assembly.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 154 cm (61 IN) APPX 1.5ml Recalled by ICU Medical, Inc. Due to Due to the...
The Issue: Due to the incorrect filter assembly.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 7 IN (18cm) APPX 0.43ml Recalled by ICU Medical, Inc. Due to Due to the...
The Issue: Due to the incorrect filter assembly.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 60 IN (152cm) APPX 1.5 ml Recalled by ICU Medical, Inc. Due to Due to the...
The Issue: Due to the incorrect filter assembly.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM 1300 Analyzer - In vitro diagnostic testing of Recalled by...
The Issue: Multiple issues in Software v1.23.2 and lower-may lead to the reporting of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH 930 Analyzer - In vitro diagnostic testing of Recalled by...
The Issue: Multiple issues in Software v1.23.2 and lower-may lead to the reporting of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM 1600 Analyzer - In vitro diagnostic testing of Recalled by...
The Issue: Multiple issues in Software v1.23.2 and lower-may lead to the reporting of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.