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. 2,939 recalls have been distributed to Florida in the last 12 months.

55,837 total recalls
2,939 in last 12 months

Showing 29012920 of 30,686 recalls

Medical DeviceOctober 4, 2024· Stryker Corporation

Recalled Item: Stryker Neptune SafeAir Smoke Evacuation Pencil Coated Rocker-Switch...

The Issue: There is a potential for the product to activate without manual input when...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: CARROLLTON HIP FX Convenience kit used for surgical procedures Recalled by...

The Issue: Products within a Medline pack may be impacted by a packaging error in which...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2024· Stryker Corporation

Recalled Item: Stryker Neptune SafeAir Smoke Evacuation Pencil Recalled by Stryker...

The Issue: There is a potential for the product to activate without manual input when...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2024· Stryker Corporation

Recalled Item: Stryker Neptune SafeAir Smoke Evacuation Pencil Coated Push-Button Recalled...

The Issue: There is a potential for the product to activate without manual input when...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: ARTHROSCOPY Convenience kit used for surgical procedures Recalled by MEDLINE...

The Issue: Products within a Medline pack may be impacted by a packaging error in which...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2024· Getinge Usa Sales Inc

Recalled Item: MEERA CL mobile operating table - Designed for the placement Recalled by...

The Issue: Error code "50037" occurs on the IR-Hand Control when a MEERA-table is...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2024· Getinge Usa Sales Inc

Recalled Item: MEERA CL mobile operating table - Designed for the placement Recalled by...

The Issue: Error code "50037" occurs on the IR-Hand Control when a MEERA-table is...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2024· Getinge Usa Sales Inc

Recalled Item: MEERA CL mobile operating table - Designed for the placement Recalled by...

The Issue: Error code "50037" occurs on the IR-Hand Control when a MEERA-table is...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2024· Getinge Usa Sales Inc

Recalled Item: MEERA CL mobile operating table - Designed for the placement Recalled by...

The Issue: Error code "50037" occurs on the IR-Hand Control when a MEERA-table is...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2024· Getinge Usa Sales Inc

Recalled Item: MEERA CL mobile operating table - Designed for the placement Recalled by...

The Issue: Error code "50037" occurs on the IR-Hand Control when a MEERA-table is...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2024· Getinge Usa Sales Inc

Recalled Item: MEERA CL mobile operating table - Designed for the placement Recalled by...

The Issue: Error code "50037" occurs on the IR-Hand Control when a MEERA-table is...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2024· DeRoyal Industries Inc

Recalled Item: DeRoyal CHILDREN'S LAPTRACEPACK Recalled by DeRoyal Industries Inc Due to...

The Issue: DeRoyal is recalling certain lots of surgical procedure pack products that...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2024· Getinge Usa Sales Inc

Recalled Item: MEERA CL mobile operating table - Designed for the placement Recalled by...

The Issue: Error code "50037" occurs on the IR-Hand Control when a MEERA-table is...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2024· Getinge Usa Sales Inc

Recalled Item: MEERA CL mobile operating table - Designed for the placement Recalled by...

The Issue: Error code "50037" occurs on the IR-Hand Control when a MEERA-table is...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2024· DeRoyal Industries Inc

Recalled Item: DeRoyal CHILDREN'S ORTHOPEDIC TRACEPACK Recalled by DeRoyal Industries Inc...

The Issue: DeRoyal is recalling certain lots of surgical procedure pack products that...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2024· DeRoyal Industries Inc

Recalled Item: DeRoyal CHILDREN'S GENERAL TRACEPACK Recalled by DeRoyal Industries Inc Due...

The Issue: DeRoyal is recalling certain lots of surgical procedure pack products that...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2024· GE Healthcare

Recalled Item: GE Healthcare Centricity Universal Viewer Zero Footprint Recalled by GE...

The Issue: GE HealthCare has become aware of an issue in Centricity Universal Viewer...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2024· DeRoyal Industries Inc

Recalled Item: DeRoyal C-SECTION TRACEPACK Recalled by DeRoyal Industries Inc Due to...

The Issue: DeRoyal is recalling certain lots of surgical procedure pack products that...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2024· Limacorporate S.p.A

Recalled Item: TEMA Elbow - Axle Small .15.010 TEMA Elbow - Recalled by Limacorporate S.p.A...

The Issue: Due to a potential difference in mechanical behavior between the implanted...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2024· Smith & Nephew Medical, Ltd.

Recalled Item: RENASYS EDGE The RENASYS¿ EDGE pump is indicated for patients Recalled by...

The Issue: Due to issues with battery depletion and inability to recharge if the...

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

Class II — Potential Health HazardOngoing