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. 2,457 recalls have been distributed to Delaware in the last 12 months.

48,330 total recalls
2,457 in last 12 months

Showing 2522125240 of 27,373 recalls

Medical DeviceMay 6, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension(R) Chemistry Wash (RD701) Recalled by Siemens Healthcare...

The Issue: Siemens Healthcare Diagnostics received complaints of Chemistry Wash causing...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2013· Covidien LP

Recalled Item: Versaport Bladeless Optical Trocar With Fixation Cannula - 5mm Short...

The Issue: Seals may disengage from the cannula which may result in a component...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2013· Covidien LP

Recalled Item: Versaport Bladeless Optical Fixation Cannula - 5mm Short Product Code:...

The Issue: Seals may disengage from the cannula which may result in a component...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2013· Intuitive Surgical, Inc.

Recalled Item: da Vinci 5 mm Flared Instrument Cannulae for use with Recalled by Intuitive...

The Issue: Intuitive Surgical is implementing a voluntary Field Action to implement a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2013· Covidien LP

Recalled Item: Versaport Bladeless Optical Trocar With Fixation Cannula - 5mm Product...

The Issue: Seals may disengage from the cannula which may result in a component...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2013· Ortho-Clinical Diagnostics

Recalled Item: 1) VITROS 5 Recalled by Ortho-Clinical Diagnostics Due to There is evidence...

The Issue: There is evidence that an electrical short within the systems connector has...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2013· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens RAD Fluoro Uro Systems - Luminos dRF Recalled by Siemens Medical...

The Issue: Siemens has discovered through product monitoring a potential malfunction...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2013· Ortho-Clinical Diagnostics

Recalled Item: VITROS 5600 Integrated System (product code 6802413) Product Usage: For...

The Issue: There is evidence that an electrical short within the systems connector has...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2013· The Anspach Effort, Inc.

Recalled Item: Anspach MIA 16 (16cm Minimally Invasive Attachment) Recalled by The Anspach...

The Issue: Product did not reach expected sterility assurance level

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2013· Ortho-Clinical Diagnostics

Recalled Item: ORTHO¿ Assay Software (OAS) Server Recalled by Ortho-Clinical Diagnostics...

The Issue: There is evidence that an electrical short within the systems connector has...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2013· Merge Healthcare, Inc.

Recalled Item: RadSuite software. The firm name on the label is Merge Healthcare Recalled...

The Issue: Multiple studies were missing at a customer location that never made it to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2013· Surgical Instrument Service And Savings, Inc.

Recalled Item: - Average Medium Blade 9mm x 25mm x 0.38mm Ref. 2296-3-111 Lot 122590...

The Issue: The seal which maintains a sterile barrier for reprocessed medical devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2013· Surgical Instrument Service And Savings, Inc.

Recalled Item: Large Tear Cross Cut Rasp 14mm x 7mm Ref. 5100-37-114 Recalled by Surgical...

The Issue: The seal which maintains a sterile barrier for reprocessed medical devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2013· DePuy Orthopaedics, Inc.

Recalled Item: DePuy Glenosphere orientation guide Product Usage: The glenosphere...

The Issue: The Glenosphere Orientation Guide Instrument Used with the Delta XTEND...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2013· Surgical Instrument Service And Savings, Inc.

Recalled Item: - Relieva Flex Sinus Guide Catheter (Green) Tip Shape: F-70 Recalled by...

The Issue: The seal which maintains a sterile barrier for reprocessed medical devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2013· Surgical Instrument Service And Savings, Inc.

Recalled Item: - CLEAR-TRAC COMPLETE Recalled by Surgical Instrument Service And Savings,...

The Issue: The seal which maintains a sterile barrier for reprocessed medical devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2013· Surgical Instrument Service And Savings, Inc.

Recalled Item: -Scorpion Needle Recalled by Surgical Instrument Service And Savings, Inc....

The Issue: The seal which maintains a sterile barrier for reprocessed medical devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2013· Surgical Instrument Service And Savings, Inc.

Recalled Item: -Instratek Carpal Tunnel Release Blades Recalled by Surgical Instrument...

The Issue: The seal which maintains a sterile barrier for reprocessed medical devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2013· Surgical Instrument Service And Savings, Inc.

Recalled Item: - Calf Garment Standard Ref. L501-M Lot 122549 Recalled by Surgical...

The Issue: The seal which maintains a sterile barrier for reprocessed medical devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2013· Surgical Instrument Service And Savings, Inc.

Recalled Item: - IDEAL 30 Suture Grasper (Green) 30 Degree Ref. 251721 Recalled by Surgical...

The Issue: The seal which maintains a sterile barrier for reprocessed medical devices...

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

Class II — Potential Health HazardOngoing