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. 2,572 recalls have been distributed to Delaware in the last 12 months.

48,330 total recalls
2,572 in last 12 months

Showing 1706117080 of 27,373 recalls

Medical DeviceJune 7, 2017· DeRoyal Industries Inc

Recalled Item: DeRoyal(R) Dolphin Inflation Device Recalled by DeRoyal Industries Inc Due...

The Issue: Lack of sterility assurance. There is a defect in the primary packaging of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2017· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Core 128 (Model No. 728323) Recalled by Philips Medical Systems...

The Issue: It was reported that scanners running certain software versions provide...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2017· Cenorin, LLC

Recalled Item: ThermaSure(TM) Recalled by Cenorin, LLC Due to Dryer unit not heating....

The Issue: Dryer unit not heating. Manufacturing issue causes the terminal block to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2017· Terumo Medical Corp

Recalled Item: Glidesheath Slender Hydrophilic Coated Introducer Sheath Recalled by Terumo...

The Issue: An incomplete seal at the chevron end of the primary packaging of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2017· Cenorin, LLC

Recalled Item: ThermaSure(TM) Recalled by Cenorin, LLC Due to Dryer unit not heating....

The Issue: Dryer unit not heating. Manufacturing issue causes the terminal block to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2017· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance 64 (Model No. 728231) Recalled by Philips Medical Systems...

The Issue: It was reported that scanners running certain software versions provide...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2017· Terumo Medical Corp

Recalled Item: Glidesheath Slender Hydrophilic Coated Introducer Sheath Recalled by Terumo...

The Issue: An incomplete seal at the chevron end of the primary packaging of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2017· Terumo Medical Corp

Recalled Item: Glidesheath Slender Hydrophilic Coated Introducer Sheath Recalled by Terumo...

The Issue: An incomplete seal at the chevron end of the primary packaging of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2017· Terumo Medical Corp

Recalled Item: Glidesheath Slender Hydrophilic Coated Introducer Sheath Recalled by Terumo...

The Issue: An incomplete seal at the chevron end of the primary packaging of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2017· Terumo Medical Corp

Recalled Item: Glidesheath Slender Hydrophilic Coated Introducer Sheath Recalled by Terumo...

The Issue: An incomplete seal at the chevron end of the primary packaging of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2017· Terumo Medical Corp

Recalled Item: Glidesheath Slender Hydrophilic Coated Introducer Sheath Recalled by Terumo...

The Issue: An incomplete seal at the chevron end of the primary packaging of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2017· Terumo Medical Corp

Recalled Item: Glidesheath Slender Hydrophilic Coated Introducer Sheath A-Kit Recalled by...

The Issue: An incomplete seal at the chevron end of the primary packaging of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2017· Terumo Medical Corp

Recalled Item: Glidesheath Slender Hydrophilic Coated Introducer Sheath Recalled by Terumo...

The Issue: An incomplete seal at the chevron end of the primary packaging of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2017· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity CT (Model No. 728326) Recalled by Philips Medical Systems...

The Issue: It was reported that scanners running certain software versions provide...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2017· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance Big Bore Radiology CT (Model No. 728244) software version...

The Issue: It was reported that scanners running certain software versions provide...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2017· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Core (Model No. 728321) Recalled by Philips Medical Systems...

The Issue: It was reported that scanners running certain software versions provide...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2017· Philips Medical Systems (Cleveland) Inc

Recalled Item: IQon Spectral CT (Model No. 728332) Recalled by Philips Medical Systems...

The Issue: It was reported that scanners running certain software versions provide...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2017· Terumo Medical Corp

Recalled Item: Glidesheath Slender Hydrophilic Coated Introducer Sheath Recalled by Terumo...

The Issue: An incomplete seal at the chevron end of the primary packaging of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2017· Terumo Medical Corp

Recalled Item: Glidesheath Slender Hydrophilic Coated Introducer Sheath A-Kit Recalled by...

The Issue: An incomplete seal at the chevron end of the primary packaging of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2017· Terumo Medical Corp

Recalled Item: Glidesheath Slender Hydrophilic Coated Introducer Sheath A-Kit Recalled by...

The Issue: An incomplete seal at the chevron end of the primary packaging of the...

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

Class II — Potential Health HazardOngoing