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. 2,469 recalls have been distributed to Delaware in the last 12 months.

48,330 total recalls
2,469 in last 12 months

Showing 2364123660 of 27,373 recalls

Medical DeviceMarch 25, 2014· Hospira Inc.

Recalled Item: LATEX-FREE Recalled by Hospira Inc. Due to The Tyvek cover may not be...

The Issue: The Tyvek cover may not be completely sealed to the rest of the package...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2014· Hospira Inc.

Recalled Item: LATEX-FREE Recalled by Hospira Inc. Due to The Tyvek cover may not be...

The Issue: The Tyvek cover may not be completely sealed to the rest of the package...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2014· AlloSource, Inc.

Recalled Item: AlloFuse DBM Putty 5cc Recalled by AlloSource, Inc. Due to The donor was...

The Issue: The donor was hemodiluted.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2014· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens ADVIA Centaur Folate Cat No. 06891541 SMN 10325366 (500 Recalled by...

The Issue: Serum controls may go out of range low with the ADVIA Centaur ¿Systems...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2014· Hospira Inc.

Recalled Item: LATEX-FREE Recalled by Hospira Inc. Due to The Tyvek cover may not be...

The Issue: The Tyvek cover may not be completely sealed to the rest of the package...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2014· Draeger Medical, Inc.

Recalled Item: Reusable latex breathing bags with multiple part numbers and sold Recalled...

The Issue: Reusable latex breathing bags with various part numbers and sold as part of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2014· Hospira Inc.

Recalled Item: LATEX-FREE Recalled by Hospira Inc. Due to The Tyvek cover may not be...

The Issue: The Tyvek cover may not be completely sealed to the rest of the package...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2014· Hospira Inc.

Recalled Item: LATEX-FREE Recalled by Hospira Inc. Due to The Tyvek cover may not be...

The Issue: The Tyvek cover may not be completely sealed to the rest of the package...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2014· Arrow International Inc

Recalled Item: Arrow Pressure Injectable PICC Powered by Arrow VPS Stylet Catalogue...

The Issue: Kits are packaged with the incorrect catheter. The kits contain a 40cm...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2014· Soma Access Systems LLC

Recalled Item: AxoTrack I Sterile Procedure Kit 18G Recalled by Soma Access Systems LLC Due...

The Issue: There is a possibility the sterile packaging may fail before the expiration...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2014· Maquet Datascope Corp - Cardiac Assist Division

Recalled Item: Datascope System 98/98xt Recalled by Maquet Datascope Corp - Cardiac Assist...

The Issue: Potential mechanical failure of the fan assembly associated with the power...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 21, 2014· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens SOMATOM Emotion 16 Recalled by Siemens Medical Solutions USA, Inc...

The Issue: The rubber damper may degrade and break, causing loosening of the motor...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2014· Alere San Diego, Inc.

Recalled Item: Alere Triage BNP Test for the Beckman Coulter Access Family Recalled by...

The Issue: These lots may not recover within range when tested using certain...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2014· Ortho-Clinical Diagnostics

Recalled Item: enGen (TM) Laboratory Automation System configured with Data Innovations...

The Issue: Software Anomaly: Ortho Clinical Diagnostics (OCD) has become aware that if...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2014· Medline Industries Inc

Recalled Item: Esmark Elastic Bandage (Sterile) Recalled by Medline Industries Inc Due to...

The Issue: This lot did not go through the correct sterilization procedures. This...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2014· Aspen Surgical Products, Inc.

Recalled Item: 15FR Drain Kit Full Fluted with Trocar and 100ml S-Vac Bulb Recalled by...

The Issue: The recall has been initiated due to a potential compromise of the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2014· Aspen Surgical Products, Inc.

Recalled Item: 15FR Drain Kit Recalled by Aspen Surgical Products, Inc. Due to The recall...

The Issue: The recall has been initiated due to a potential compromise of the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2014· Aspen Surgical Products, Inc.

Recalled Item: 10FR Drain Kit Full Fluted with Trocar and 100ml S-Vac Bulb Recalled by...

The Issue: The recall has been initiated due to a potential compromise of the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2014· Aspen Surgical Products, Inc.

Recalled Item: 7mm Drain Kit Fluted 4 Channel with 100ml S-Vac Bulb Recalled by Aspen...

The Issue: The recall has been initiated due to a potential compromise of the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2014· Aspen Surgical Products, Inc.

Recalled Item: Saber 100ml Infection Control PVC Bulb with 150ml 3C System Recalled by...

The Issue: The recall has been initiated due to a potential compromise of the sterile...

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

Class II — Potential Health HazardOngoing