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. 2,918 recalls have been distributed to Florida in the last 12 months.
Showing 5161–5180 of 55,837 recalls
Recalled Item: AGILE ESO FC RMV 23MM X 6.2CM IN 18.5 FR-Agile Recalled by Boston Scientific...
The Issue: WallFlexTM Esophageal Stent System and AgileTM Esophageal Over the Wire...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WALLFLEX FC ESO STENT RMV 23X105MM- Wallflex Esophageal Partially Covered...
The Issue: WallFlexTM Esophageal Stent System and AgileTM Esophageal Over the Wire...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WALLFLEX PC ESOPH STENT 18/23MM X 153MM- Wallflex Esophageal Partially...
The Issue: WallFlexTM Esophageal Stent System and AgileTM Esophageal Over the Wire...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WALLFLEX FC ESO STENT RMV 18X123MM-Wallflex Esophageal Partially Covered...
The Issue: WallFlexTM Esophageal Stent System and AgileTM Esophageal Over the Wire...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WALLFLEX PC ESOPH STENT 23/28MM X 125MM- Wallflex Esophageal Partially...
The Issue: WallFlexTM Esophageal Stent System and AgileTM Esophageal Over the Wire...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Phoenix 100-Intended for the rapid identification (ID) and antimicrobial...
The Issue: Escherichia coli (E. coli) misidentification for clinical samples that were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WALLFLEX ESOPHAGEAL FC 18/23-25MMX10CM- Wallflex Esophageal Partially...
The Issue: WallFlexTM Esophageal Stent System and AgileTM Esophageal Over the Wire...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MiniMed 620G Insulin Pump Recalled by Medtronic MiniMed, Inc. Due to Insulin...
The Issue: Insulin pumps that have been dropped, bumped, or experienced physical impact...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MiniMed Insulin Pump Device. MiniMed 670G Recalled by Medtronic MiniMed,...
The Issue: Insulin pumps that have been dropped, bumped, or experienced physical impact...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Silver-Plated Copper Sims Uterine Sound Recalled by CooperSurgical, Inc. Due...
The Issue: During the manufacturing process the devices were laser-marked with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stainless Steel Sims Uterine Sound Recalled by CooperSurgical, Inc. Due to...
The Issue: During the manufacturing process the devices were laser-marked with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Inspire Model 4340 Respiratory Sensing Lead Recalled by Inspire Medical...
The Issue: Labeling error with a mismatch between the shelf box serial number label and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMAGE Immunochemistry Systems IGM Immunoglobulin M Reagent IGM Recalled by...
The Issue: Firm identified two lots of reagents that are not meeting the sensitivity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MiniMed 630G Insulin Pump Recalled by Medtronic MiniMed, Inc. Due to Insulin...
The Issue: Insulin pumps that have been dropped, bumped, or experienced physical impact...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Inspire Model 4063 Stimulation Lead Recalled by Inspire Medical Systems Inc....
The Issue: Labeling error with a mismatch between the shelf box serial number label and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Indomethacin Extended-Release Capsules Recalled by Glenmark Pharmaceuticals...
The Issue: Failed Dissolution Specifications: below specification results
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Gabapentin Tablets Recalled by Granules Pharmaceuticals Inc. Due to Presence...
The Issue: Presence of Foreign Tablets; 3 fused tablets of Metformin ER 500 mg were...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Boars Head Grab and Go Wedge Ham Recalled by Publix Super Markets, Inc. Due...
The Issue: Potential Listeria Monocytogenes
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Ground cinnamon. Supreme Tradition brand ground cinnamon packaged in 2.25...
The Issue: Elevated lead levels in cinnamon
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Dimension Vista¿ Total Bilirubin (TBIL) Flex Reagent Cartridge Recalled by...
The Issue: During manufacturing, the last three tests from the 160 test flex of lot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.