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. 2,630 recalls have been distributed to Delaware in the last 12 months.

48,330 total recalls
2,630 in last 12 months

Showing 1116111180 of 27,373 recalls

Medical DeviceJuly 24, 2020· Ra Medical Systems, Inc.

Recalled Item: DABRA RA-308 Excimer Laser Recalled by Ra Medical Systems, Inc. Due to Due...

The Issue: Due to the taller wheel mounting on the laser, the laser may fall over...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2020· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista High Sensitivity Troponin I (TNIH) Flex reagent...

The Issue: Dimension Vista High Sensitivity Troponin I (TNIH) may exhibit a negative...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens Sensis Vibe Hemo system in combination with the MicroPodTM Recalled...

The Issue: The connector linking the EtCO2 module to the HemoBox may break and become...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2020· Intrinsic Therapeutics, Inc.

Recalled Item: Barricaid Annual Closure Device (ACD) BAR-A8-8MM - Product Usage: The...

The Issue: The catalog ( REF ) number on the peelable inner labels (patient sticker)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2020· Remel Europe Ltd.

Recalled Item: Thermo Scientific Remel Bordetella pertussis Agglutinating Serum Product...

The Issue: Thermo Scientific" Remel" Bordetella pertussis Agglutinating Serum...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2020· Philips Medical Systems Gmbh, DMC

Recalled Item: CombiDiagnost R90 Software Version R1.0 and R1.1 Recalled by Philips Medical...

The Issue: Philips has become aware of a software issue, where the kV and mA values are...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2020· Smith & Nephew Orthopaedics AG

Recalled Item: POLARSTEM COLLAR Reamer Guide Recalled by Smith & Nephew Orthopaedics AG Due...

The Issue: Multiple lots being recalled due to a product design issue

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2020· BEYOND WHITE SPA LLC D.B.A. EZYWIPE OF AMERCIA

Recalled Item: Ezycare Face Mask Recalled by BEYOND WHITE SPA LLC D.B.A. EZYWIPE OF AMERCIA...

The Issue: Disposable face masks labeled as non-medical were distributed to customers...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2020· Neurovision Medical Products Inc

Recalled Item: Nerveana x5 RLN Monitoring Kit with Cobra 1-Ch EMG ET Tube Recalled by...

The Issue: The electrode insulating material on the Cobra EMG ET tube used for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2020· Neurovision Medical Products Inc

Recalled Item: Cobra x5 2-Ch EMG ET Tube Recalled by Neurovision Medical Products Inc Due...

The Issue: The electrode insulating material on the Cobra EMG ET tube used for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2020· Neurovision Medical Products Inc

Recalled Item: Cobra x5 1-CH EMG ET Tube Recalled by Neurovision Medical Products Inc Due...

The Issue: The electrode insulating material on the Cobra EMG ET tube used for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2020· Neurovision Medical Products Inc

Recalled Item: Cobra x5 1-Ch EMG ET Tube Recalled by Neurovision Medical Products Inc Due...

The Issue: The electrode insulating material on the Cobra EMG ET tube used for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2020· Neurovision Medical Products Inc

Recalled Item: Nerveana x5 RLN Monitoring Kit with Cobra 1-Ch EMG ET Tube Recalled by...

The Issue: The electrode insulating material on the Cobra EMG ET tube used for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2020· Neurovision Medical Products Inc

Recalled Item: Cobra x5 1-Ch EMG ET Tube Recalled by Neurovision Medical Products Inc Due...

The Issue: The electrode insulating material on the Cobra EMG ET tube used for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2020· Neurovision Medical Products Inc

Recalled Item: Cobra x5 2-Ch EMG ET Tube Recalled by Neurovision Medical Products Inc Due...

The Issue: The electrode insulating material on the Cobra EMG ET tube used for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2020· Neurovision Medical Products Inc

Recalled Item: Nerveana x5 RLN Monitoring Kit with Cobra 1-Ch EMT ET Tube Recalled by...

The Issue: The electrode insulating material on the Cobra EMG ET tube used for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2020· Neurovision Medical Products Inc

Recalled Item: Cobra x5 2-Ch EMG ET Tube Recalled by Neurovision Medical Products Inc Due...

The Issue: The electrode insulating material on the Cobra EMG ET tube used for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2020· Synthes (USA) Products LLC

Recalled Item: DePuy Synthes Trauma LCP One-Third Tubular Plate with Collar 8 Recalled by...

The Issue: May have one or more dimensional features out of tolerance includes: thread...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2020· ARJOHUNTLEIGH POLSKA Sp. z.o.o.

Recalled Item: Bariatric Bed Frame System The Citadel Plus Bariatric Bed Frame Recalled by...

The Issue: Modular Junction Box (MJB) cables can melt and affect the bed functionality.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2020· Ortho Clinical Diagnostics

Recalled Item: VITROS XT7600 Integrated System Recalled by Ortho Clinical Diagnostics Due...

The Issue: When processing MicroSlides, slides that utilize Slot 18 in the CM rotor may...

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

Class II — Potential Health HazardOngoing