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 1962119640 of 27,373 recalls

Medical DeviceMarch 17, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista Assays: Enzymatic Creatine (ECRE) Recalled by Siemens...

The Issue: Siemens Healthcare Diagnostics has become aware of N-Acetylcysteine (NAC)...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2016· Medtronic Navigation, Inc.-Littleton

Recalled Item: Medtronic Navigation O-arm 02 surgical x-ray imaging system Recalled by...

The Issue: Review of on-system electronic product labeling and Instr uctions for Use in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Assays: Uric Acid (URCA) Recalled by Siemens Healthcare...

The Issue: Siemens Healthcare Diagnostics has become aware of N-Acetylcysteine (NAC)...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Advia Chemistry Assay: LDL Cholesterol Recalled by Siemens Healthcare...

The Issue: Siemens Healthcare Diagnostics has become aware of N-Acetylcysteine (NAC)...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2016· Intuitive Surgical, Inc.

Recalled Item: da Vinci S Surgical System (IS1200/IS2000/IS3000) user manual Recalled by...

The Issue: Intuitive Surgical has found that the use of instruments other than the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2016· Terumo Medical Corporation

Recalled Item: PINNACLE¿ Introducer Sheath PINNACLE PRECISION ACCESS SYSTEM¿ Sheath...

The Issue: Terumo Medical is initiating this recall due to complaints of valve leakage...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2016· Intuitive Surgical, Inc.

Recalled Item: da Vinci S Surgical System (IS4000) user manual English and Recalled by...

The Issue: Intuitive Surgical has found that the use of instruments other than the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2016· Invacare Corporation

Recalled Item: Invacare¿ Bariatric Bed with mattress and rails Recalled by Invacare...

The Issue: The firm recently identified a quality issue with the Junction box used in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2016· Invacare Corporation

Recalled Item: Invacare¿ Foot Section for Semi & Full Electric Beds Recalled by Invacare...

The Issue: The firm recently identified a quality issue with the Junction box used in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2016· Mevion Medical Systems, Inc.

Recalled Item: MEVION S250 for Proton Radiation Therapy Recalled by Mevion Medical Systems,...

The Issue: Possibility of Gantry Motion with Aperture or Compensator only partially...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2016· Philips Electronics North America Corporation

Recalled Item: Philips Healthcare System X-ray Tomography Computed : Recalled by Philips...

The Issue: It was discovered the patient support tabletop may fail to move in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2016· Invacare Corporation

Recalled Item: Junction Boxes Recalled by Invacare Corporation Due to The firm recently...

The Issue: The firm recently identified a quality issue with the Junction box used in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2016· Ventlab LLC

Recalled Item: STAT-Check Resuscitation Bag Manual Emergency Resuscitation Bag with Carbon...

The Issue: Stat-check CO2 indicators are non-functional. The indicator is yellow when...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2016· Olympus Corporation of the Americas

Recalled Item: EVIS EXERA Duodenovideoscope Olympus TJF Type 160F/VF used with an Recalled...

The Issue: New reprocessing instructions for the Olympus TJF-160/VF duodenoscopes,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2016· Philips Electronics North America Corporation

Recalled Item: Philips Healthcare System X-ray Tomography Computed : Recalled by Philips...

The Issue: It was discovered the patient support tabletop may fail to move in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2016· Invacare Corporation

Recalled Item: Invacare¿ Bariatric Bed w/o mattress & rails Recalled by Invacare...

The Issue: The firm recently identified a quality issue with the Junction box used in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2016· Ossur H / F

Recalled Item: Ossur Lil Angel Vest P2 Lambswool. Pediatric sized vest is Recalled by Ossur...

The Issue: There is a potential for partial or complete fracture of the plastic...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2016· Navilyst Medical, Inc., an AngioDyamics Company

Recalled Item: BioFlo PICC with ENDEXO and PASV Valve Technology Recalled by Navilyst...

The Issue: PICC catheters that contain valve(s) manufactured prior to July 15, 2014...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2016· Terumo Cardiovascular Systems Corporation

Recalled Item: CDI Blood Parameter Monitoring System 500 Cardiopulmonary bypass on-line...

The Issue: Specific CDI¿ Blood Parameter Monitoring System 500 devices are being...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2016· Navilyst Medical, Inc., an AngioDyamics Company

Recalled Item: BioFlo Hybrid PICC with ENDEXO and PASV Valve Technology Recalled by...

The Issue: PICC catheters that contain valve(s) manufactured prior to July 15, 2014...

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

Class II — Potential Health HazardOngoing