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. 2,940 recalls have been distributed to Florida in the last 12 months.
Showing 1381–1400 of 55,837 recalls
Recalled Item: Levothyroxine Sodium Tablets Recalled by ACCORD HEALTHCARE, INC. Due to...
The Issue: Subpotent: During long term stability testing of Levothyroxine Sodium...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Catalyft PL & PL40 Expandable Interbody System labeled as follows Recalled...
The Issue: Expandable interbody system cage may loose height or collapse (loss of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SyncAR Surgical Navigation Advanced Platform Patient Engagement (SyncAR...
The Issue: A software anomaly, under specific conditions when large rotational...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Sentinel V11 Product Name: Sentinel V11 Model/Catalog Number:...
The Issue: Due to two distinct issues: 1. During patient admission, patient demographic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surgical Planner Recalled by Surgical Theater Inc Due to A software anomaly,...
The Issue: A software anomaly, under specific conditions when large rotational...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SuRgical Planner (SRP) Recalled by Surgical Theater Inc Due to A software...
The Issue: A software anomaly, under specific conditions when large rotational...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endo Surgical Navigation Advanced Platform Patient Engagement (EndoSNAP)...
The Issue: A software anomaly, under specific conditions when large rotational...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SpineAR Surgical Navigation Advanced Platform Patient Engagement (SyncAR...
The Issue: A software anomaly, under specific conditions when large rotational...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surgical Navigation Advanced Platform (SNAP) Recalled by Surgical Theater...
The Issue: A software anomaly, under specific conditions when large rotational...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surgical Navigation Advanced Platform Patient Engagement (PE SNAP) Recalled...
The Issue: A software anomaly, under specific conditions when large rotational...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Automated Impella Controller (AIC) labeled as the following with...
The Issue: Potential for Automated Impella Controller (AIC) purge pressure issues due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bupropion Hydrochloride Extended-Release Tablets USP (XL) Recalled by...
The Issue: Failed Tablet/Capsule Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Carbamazepine Extended-Release Tablets Recalled by Amerisource Health...
The Issue: Failed Dissolution Specifications.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CONSTELLATION ULTRAVIT 10K and CONSTELLATION HYPERVIT 20K Recalled by Alcon...
The Issue: XXX
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FDR Visionary Suite Recalled by FUJIFILM Healthcare Americas Corporation Due...
The Issue: It was found that the shaft for mounting the X-ray tube unit on the support...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Organic BABY bedtime drops Recalled by M.O.M Enterprises, LLC. Due to...
The Issue: Potential yeast contamination.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Cetirizine Hydrochloride Tablets USP 10 mg Recalled by JB Chemicals and...
The Issue: Tablet/Capsules Imprinted with Wrong ID
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cetirizine Hydrochloride Tablets USP 10 mg Recalled by JB Chemicals and...
The Issue: Tablet/Capsules Imprinted with Wrong ID
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Major ChlorproMAZINE Hydrochloride Tablets Recalled by The Harvard Drug...
The Issue: CGMP Deviations: Presence of N-Nitroso Desmethyl Chlorpromazine above the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Major ChlorproMAZINE Hydrochloride Tablets Recalled by The Harvard Drug...
The Issue: CGMP Deviations: Presence of N-Nitroso Desmethyl Chlorpromazine above the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.