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. 1,111 recalls have been distributed to Florida in the last 12 months.

55,837 total recalls
1,111 in last 12 months

Showing 16581–16600 of 30,686 recalls

Medical DeviceJuly 11, 2018· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products Cl- Slides Recalled by Ortho-Clinical Diagnostics...

The Issue: The slides do not meet the maximum allowable interference (MAI) claims for...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceJuly 11, 2018· COVIDIEN LLC

Recalled Item: P400 PREM U/M 16FR TMPSNS Recalled by COVIDIEN LLC Due to The temperature...

The Issue: The temperature sensor catheters may be defective in that they will show a...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 11, 2018· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products Cl- Slides Recalled by Ortho-Clinical Diagnostics...

The Issue: The slides do not meet the maximum allowable interference (MAI) claims for...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceJuly 11, 2018· COVIDIEN LLC

Recalled Item: P400 PREM U/M 18FR TMPSNS Recalled by COVIDIEN LLC Due to The temperature...

The Issue: The temperature sensor catheters may be defective in that they will show a...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 11, 2018· COVIDIEN LLC

Recalled Item: 400mL Recalled by COVIDIEN LLC Due to The temperature sensor catheters may...

The Issue: The temperature sensor catheters may be defective in that they will show a...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 11, 2018· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products CREA Slides Recalled by Ortho-Clinical Diagnostics...

The Issue: The slides did not meet the current claims for Limit of Blank (LoB), Limit...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceJuly 11, 2018· POM Medical LLC

Recalled Item: POM Procedural Oxygen Masks Recalled by POM Medical LLC Due to Complaints...

The Issue: Complaints were received on the product, such as the re-breather bag would...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 10, 2018· Arrow International Inc

Recalled Item: HANDS-OFF Multi-Lumen Central Venous Catheter with Blue FlexTip for use...

The Issue: The packaging may not be sealed. If the packaging is compromised in this...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 10, 2018· Arrow International Inc

Recalled Item: HANDS-OFF Multi-Lumen Central Venous Catheter with Blue FlexTip for use...

The Issue: The packaging may not be sealed. If the packaging is compromised in this...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 9, 2018· Sorin CRM SAS

Recalled Item: Sorin Platinium CRT-D 1711 DF-1 Recalled by Sorin CRM SAS Due to Hardware...

The Issue: Hardware configuration may lead to overconsumption, followed by loss of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 9, 2018· Sorin CRM SAS

Recalled Item: Sorin Platinium CRT-D 1741 DF-4 Recalled by Sorin CRM SAS Due to Hardware...

The Issue: Hardware configuration may lead to overconsumption, followed by loss of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 9, 2018· Merit Medical Systems, Inc.

Recalled Item: ChloraPrep With Tint Recalled by Merit Medical Systems, Inc. Due to A...

The Issue: A nonsterile bulk product designated for further processing in a tray was...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2018· Smiths Medical ASD Inc.

Recalled Item: smiths medical portex First Breath Adult Nasal Cannula Recalled by Smiths...

The Issue: "Manufactured" and "Use By" labels are transposed incorrectly suggesting the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceJuly 6, 2018· Smiths Medical ASD Inc.

Recalled Item: smiths medical portex First Breath Adult Nasal Cannula Recalled by Smiths...

The Issue: "Manufactured" and "Use By" labels are transposed incorrectly suggesting the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceJuly 6, 2018· Smiths Medical ASD Inc.

Recalled Item: smiths medical portex First Breath Nasal Oxygen Cannula Recalled by Smiths...

The Issue: "Manufactured" and "Use By" labels are transposed incorrectly suggesting the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceJuly 6, 2018· Smiths Medical ASD Inc.

Recalled Item: smiths medical portex First Breath Nasal Oxygen Cannula Recalled by Smiths...

The Issue: "Manufactured" and "Use By" labels are transposed incorrectly suggesting the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceJuly 6, 2018· Neotract Inc

Recalled Item: UroLift System Number: UL400-4 Tray Contents: UroLift System Recalled by...

The Issue: Upon implant deployment, the Capsular Tab may not be delivered as the needle...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2018· Smiths Medical ASD Inc.

Recalled Item: smiths medical portex First Breath Adult Nasal Cannula Recalled by Smiths...

The Issue: "Manufactured" and "Use By" labels are transposed incorrectly suggesting the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceJuly 6, 2018· 3M Company - Health Care Business

Recalled Item: 3M Fast Release Varnish Recalled by 3M Company - Health Care Business Due to...

The Issue: Product has an unpleasant flavor due to a manufacturing process error...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2018· Radiometer America Inc

Recalled Item: ABL800 analyzer Recalled by Radiometer America Inc Due to The analyzer...

The Issue: The analyzer software may cause a mis-match of patient demographics and test...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing