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. 2,706 recalls have been distributed to Florida in the last 12 months.
Showing 31401–31420 of 55,837 recalls
Recalled Item: SORIN GROUP Recalled by Sorin Group USA, Inc. Due to Medtronic informed...
The Issue: Medtronic informed LivaNova that some of their DLP Pressure Disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SORIN GROUP Recalled by Sorin Group USA, Inc. Due to Medtronic informed...
The Issue: Medtronic informed LivaNova that some of their DLP Pressure Disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STERILE SAMPLE SORIN GROUP Recalled by Sorin Group USA, Inc. Due to...
The Issue: Medtronic informed LivaNova that some of their DLP Pressure Disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Suction 9734308 Small AxiEM ENT Recalled by Medtronic Navigation,...
The Issue: The instruments are not able to pass instrument verification which is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SORIN GROUP Recalled by Sorin Group USA, Inc. Due to Medtronic informed...
The Issue: Medtronic informed LivaNova that some of their DLP Pressure Disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SORIN GROUP Recalled by Sorin Group USA, Inc. Due to Medtronic informed...
The Issue: Medtronic informed LivaNova that some of their DLP Pressure Disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Curved Suction 90 9733451 EM ENT Recalled by Medtronic Navigation,...
The Issue: The instruments are not able to pass instrument verification which is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Set Supplemental INS AxiEM ENT Recalled by Medtronic Navigation,...
The Issue: The instruments are not able to pass instrument verification which is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Instrument Kit 9733908 Fusion ENT Recalled by Medtronic...
The Issue: The instruments are not able to pass instrument verification which is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Curved Suction 70 9733450 EM ENT Recalled by Medtronic Navigation,...
The Issue: The instruments are not able to pass instrument verification which is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SORIN GROUP Recalled by Sorin Group USA, Inc. Due to Medtronic informed...
The Issue: Medtronic informed LivaNova that some of their DLP Pressure Disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic ENT Prgm 9734636 Add Fusion Nav AxiEM Recalled by Medtronic...
The Issue: The instruments are not able to pass instrument verification which is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EMBLEM MRI S-ICD Model 219 Recalled by Boston Scientific Corporation Due to...
The Issue: The device can deliver an atypical amount of energy due to memory corruption...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Instrument Set EM ENT Recalled by Medtronic Navigation, Inc. Due...
The Issue: The instruments are not able to pass instrument verification which is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Straight Suction 9733449 EM ENT Recalled by Medtronic Navigation,...
The Issue: The instruments are not able to pass instrument verification which is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EMBLEM S-ICD Recalled by Boston Scientific Corporation Due to The device can...
The Issue: The device can deliver an atypical amount of energy due to memory corruption...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SORIN GROUP Recalled by Sorin Group USA, Inc. Due to Medtronic informed...
The Issue: Medtronic informed LivaNova that some of their DLP Pressure Disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SORIN GROUP Recalled by Sorin Group USA, Inc. Due to Medtronic informed...
The Issue: Medtronic informed LivaNova that some of their DLP Pressure Disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Buprenorphine and Naloxone Sublingual Tablets 8 mg/2 mg 30 tablets per...
The Issue: Failed Impurities/Degradation Specifications: out of specification test...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Buprenorphine and Naloxone Sublingual Tablets Recalled by Teva...
The Issue: Failed Impurities/Degradation Specifications: out of specification test...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.