Product Recalls in Delaware

Product recalls affecting Delaware — including food, drugs, consumer products, medical devices, and vehicles distributed to Delaware. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,495 recalls have been distributed to Delaware in the last 12 months.

48,330 total recalls
2,495 in last 12 months

Showing 2086120880 of 27,373 recalls

Medical DeviceAugust 24, 2015· Terumo Cardiovascular Systems Corp

Recalled Item: Terumo Custom Cardiovascular Procedure Kit X-Coated PED/Adult Main Pack P/N:...

The Issue: Custom Cardiovascular Procedure Kits contain recalled component Medivators...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2015· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens RAPIDPoint 500 Measurement Cartridge Lactate (100) tests Part...

The Issue: RAPIDPoint 500 measurement cartridge serial numbers 2517102517 through...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2015· Teleflex Medical

Recalled Item: Rusch Flexi-slip tracheal tube Stylet Recalled by Teleflex Medical Due to...

The Issue: Due to reports of the plastic coating of the stylet splitting and/or...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2015· Terumo Cardiovascular Systems Corp

Recalled Item: Terumo Custom Cardiovascular Procedure Kit X-Coated Adult Pak P/N: 73124...

The Issue: Custom Cardiovascular Procedure Kits contain recalled component Medivators...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2015· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens RAPIDPoint 500 Measurement Cartridge Lactate (400) tests Part...

The Issue: RAPIDPoint 500 measurement cartridge serial numbers 2517102517 through...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2015· Terumo Cardiovascular Systems Corp

Recalled Item: Terumo Custom Cardiovascular Procedure Kit X-Coated PED/Adult Main Pack P/N:...

The Issue: Custom Cardiovascular Procedure Kits contain recalled component Medivators...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2015· STERILMED, INC.

Recalled Item: Zimmer Recalled by STERILMED, INC. Due to Mislabeling

The Issue: Sterilmed, Inc. is recalling its reprocessed Zimmer Tourniquet Cuff, Part...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2015· Teleflex Medical

Recalled Item: R¿sch Flexi-Slip Endotracheal Tube Stylet with Soft Distal Tip Recalled by...

The Issue: Due to reports of the plastic coating of the stylet splitting and/or...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2015· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens RAPIDPoint 500 Measurement Cartridge Lactate (750 tests) Part...

The Issue: RAPIDPoint 500 measurement cartridge serial numbers 2517102517 through...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2015· Terumo Cardiovascular Systems Corp

Recalled Item: Terumo Custom Cardiovascular Procedure Kit Tubing Pack P/N: 66041-1 Terumo...

The Issue: Custom Cardiovascular Procedure Kits contain recalled component Medivators...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2015· Terumo Cardiovascular Systems Corp

Recalled Item: Terumo Custom Cardiovascular Procedure Kit X-Coated Perfusion Pack with...

The Issue: Custom Cardiovascular Procedure Kits contain recalled component Medivators...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2015· Terumo Cardiovascular Systems Corp

Recalled Item: Terumo Custom Cardiovascular Procedure Kit X-Coated Pediatric Pack P/N:...

The Issue: Custom Cardiovascular Procedure Kits contain recalled component Medivators...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2015· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens RAPIDPoint 500 Measurement Cartridge Lactate (250) tests Part...

The Issue: RAPIDPoint 500 measurement cartridge serial numbers 2517102517 through...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2015· Terumo Cardiovascular Systems Corp

Recalled Item: Terumo Custom Cardiovascular Procedure Kit X-Coated Perfusion Pack P/N:...

The Issue: Custom Cardiovascular Procedure Kits contain recalled component Medivators...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2015· Olympus Corporation of the Americas

Recalled Item: EVIS EXERA II Gastrovideoscope OLYMPUS GF type UCT180 Recalled by Olympus...

The Issue: Insufficient information for specific cleaning accessories used for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2015· DJO, LLC

Recalled Item: Monode Recalled by DJO, LLC Due to Overheating and burning of the wire...

The Issue: Overheating and burning of the wire insulation inside the applicator.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 20, 2015· Orthovita, Inc., dBA Stryker Orthobiologics.

Recalled Item: Aliquot Delivery Kit (Syringe and Plunger) Recalled by Orthovita, Inc., dBA...

The Issue: Two isolated instances of holes in the outer header bag component of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2015· Covidien LLC

Recalled Item: MediTrace Cadence Adult Multi-Function Defibrillation Electrodes Item...

The Issue: Multi-Function Defibrillation Electrodes, Pre connect- potential for damage...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2015· Covidien LLC

Recalled Item: MediTrace Cadence Adult Zoll Recalled by Covidien LLC Due to Multi-Function...

The Issue: Multi-Function Defibrillation Electrodes, Pre connect- potential for damage...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2015· Siemens Medical Solutions USA, Inc.

Recalled Item: ACUSON SC2000 Ultrasound System with software versions VB10B and lower...

The Issue: The ACUSON SC2000 ultrasound system considers uppercase/lowercase...

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

Class II — Potential Health HazardOngoing