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. 2,506 recalls have been distributed to Delaware in the last 12 months.

48,330 total recalls
2,506 in last 12 months

Showing 1888118900 of 27,373 recalls

Medical DeviceAugust 1, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Multix Fusion VA10 Product Usage: The Multix Fusion VA10 system Recalled by...

The Issue: Siemens became aware of a potential issue with the patient table for Ysio...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: YSIO Max Product Usage: The Ysio Max is a radiographic Recalled by Siemens...

The Issue: Siemens became aware of a potential issue with the patient table for Ysio...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2016· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Orthopaedics Patella Assembly Instrument Recalled by Stryker...

The Issue: Upon failure of the press-fit, the clamping sub components and pins could...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2016· Ethicon, Inc.

Recalled Item: ETHICON MERSILENE" Tape (also to as MERSILENETM Polyester Fiber Recalled by...

The Issue: ETHICON MERSILENE" Tape (also to as MERSILENETM Polyester Fiber Strip or...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2016· Zyno Medical LLC

Recalled Item: Zyno Medical Administration Set Recalled by Zyno Medical LLC Due to...

The Issue: Administration Set potential filter leaking

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2016· Zyno Medical LLC

Recalled Item: Zyno Medical Administration Set Recalled by Zyno Medical LLC Due to...

The Issue: Administration Set potential filter leaking

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2016· B. Braun Medical, Inc.

Recalled Item: Sterile IV Start Kits 50 units/trays per case Convenience kit Recalled by B....

The Issue: Positive results from non-routine sterility testing commissioned by B. Braun...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2016· Zyno Medical LLC

Recalled Item: Zyno Medical Administration Set Sterile. Rx For Use with Zyno Recalled by...

The Issue: Administration Set potential filter leaking

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2016· Zyno Medical LLC

Recalled Item: Zyno Medical Administration Set Recalled by Zyno Medical LLC Due to...

The Issue: Administration Set potential filter leaking

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2016· OrthoPediatrics Corp

Recalled Item: 3.5mm Bowed Locking Compression Femur Plates Recalled by OrthoPediatrics...

The Issue: OrthoPediatrics Corp.is voluntarily recalling multiple lots of the 3.5mm...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2016· OrthoPediatrics Corp

Recalled Item: 3.5mm Bowed Locking Compression Femur Plates Recalled by OrthoPediatrics...

The Issue: OrthoPediatrics Corp.is voluntarily recalling multiple lots of the 3.5mm...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2016· Howmedica Osteonics Corp.

Recalled Item: AccuLIF PL 6-9mm x 11mm x 27mm x 8 Cage Recalled by Howmedica Osteonics...

The Issue: Since Stryker acquired the AccuLIF product in March of 2014, there have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2016· Howmedica Osteonics Corp.

Recalled Item: AccuLIF PL 8-12mm x 11mm x 27mm x 8 Cage Recalled by Howmedica Osteonics...

The Issue: Since Stryker acquired the AccuLIF product in March of 2014, there have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: PRIMUS Recalled by Siemens Medical Solutions USA, Inc Due to Software patch...

The Issue: Software patch installation to address several safety issues.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2016· Philips Electronics North America Corporation

Recalled Item: IntelliVue Patient Monitor Product Usage: The monitors are indicated for...

The Issue: If an affected Patient Monitor has been powered on continuously for several...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: ARTISTE Recalled by Siemens Medical Solutions USA, Inc Due to Software patch...

The Issue: Software patch installation to address several safety issues.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Syngo RT Therapist Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: Software patch installation to address several safety issues.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2016· Encore Medical, Lp

Recalled Item: Cobalt HV Bone Cement Product Usage: Cobalt HV Bone Cement Recalled by...

The Issue: The outer packaging was mislabeled on the box indicating "Cobalt HV with...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2016· Howmedica Osteonics Corp.

Recalled Item: AccuLIF PL 10-16mm x 11mm x 27mm x 8 Cage Recalled by Howmedica Osteonics...

The Issue: Since Stryker acquired the AccuLIF product in March of 2014, there have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2016· Terumo Cardiovascular Systems Corp

Recalled Item: Terumo Custom Cardiovascular System Cardiovascular Procedure Kits labeled...

The Issue: Terumo Custom Cardiovascular Procedure Kits are labeled as Xcoating surface...

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

Class II — Potential Health HazardOngoing