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. 2,754 recalls have been distributed to Florida in the last 12 months.
Showing 20381–20400 of 30,686 recalls
Recalled Item: K2M Special Connector Instruments (Special Connector Recalled by K2M, Inc...
The Issue: Instruments were developed without adequate consideration given to the need...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CVS Health At Home A1C Test Kit Recalled by Polymer Technology Systems Due...
The Issue: A numerical value less than 4% or greater than 13% may be displayed instead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PreludeEASE Hydrophilic Sheath Introducer Dilator The Merit PreludeEASE...
The Issue: Recalling dilators included with the 6F PreludeEASE Hydrophilic Sheath...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Specimen Gate Laboratory 5002-0180 Recalled by PerkinElmer Health Sciences,...
The Issue: Issue may cause eReports to consume an excessive amount of disk space...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRU-Balance 3 Power Positioning Systems Recalled by Pride Mobility Products...
The Issue: The interface between the TB3 back and tilt base can separate when tilted...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8450-009-040 4.0MM Precision Round Recalled by Stryker Instruments Div. of...
The Issue: Stryker Instruments is voluntarily recalling specific lots of sterile MIS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8450-107-525 2.5MM Precision Match Head Recalled by Stryker Instruments Div....
The Issue: Stryker Instruments is voluntarily recalling specific lots of sterile MIS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AtriClip" LAA Exclusion System with preloaded Gillinov-Cosgrove" Clip - A...
The Issue: A complaint of the PRO2 jaw breaking prior to surgery being performed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ecolab Recalled by Ecolab Inc Due to The reason for the recall is that the...
The Issue: The reason for the recall is that the inner carton box of the Rolled Probe...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8450-009-030 3.0MM Precision Round Recalled by Stryker Instruments Div. of...
The Issue: Stryker Instruments is voluntarily recalling specific lots of sterile MIS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8450-010-040 4.0MM Round Recalled by Stryker Instruments Div. of Stryker...
The Issue: Stryker Instruments is voluntarily recalling specific lots of sterile MIS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8470-009-030 3.0MM Precision Round Recalled by Stryker Instruments Div. of...
The Issue: Stryker Instruments is voluntarily recalling specific lots of sterile MIS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8470-009-040 4.0MM Precision Round Recalled by Stryker Instruments Div. of...
The Issue: Stryker Instruments is voluntarily recalling specific lots of sterile MIS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8450-107-530 3.0MM Precision Match Head Recalled by Stryker Instruments Div....
The Issue: Stryker Instruments is voluntarily recalling specific lots of sterile MIS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atrium Medical Pediatric Chamber Ocean Drains as follows: 2012-320 Ocean...
The Issue: Outer Packaging is not sterile
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atrium Medical 400 Series Express Drains as follows: 4000-100N Express...
The Issue: Outer Packaging is not sterile
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atrium Medical Dual Chamber Ocean Drains as follows: 2020-000 Ocean Recalled...
The Issue: Outer Packaging is not sterile
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atrium Medical Oasis Pediatric Drain as follows: 3612-100 Oasis...
The Issue: Outer Packaging is not sterile
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atrium Medical Oasis Single Drain as follows: 3600-100 Oasis single Recalled...
The Issue: Outer Packaging is not sterile
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atrium Medical Ocean Drains as follows: 2002-000 Ocean single drain Recalled...
The Issue: Outer Packaging is not sterile
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.