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 2068120700 of 27,373 recalls

Medical DeviceOctober 23, 2015· Fresenius Medical Care Renal Therapies Group, LLC

Recalled Item: Fresenius 132 Gallon GranuFlo Dissolution Unit - P/N G047-80101. For...

The Issue: Dissolution units and replacement motors units do not provide full thermal...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2015· GE Medical Systems, LLC

Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to GE Healthcare has...

The Issue: GE Healthcare has recently become aware of a potential issue with routine...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2015· Fresenius Medical Care Renal Therapies Group, LLC

Recalled Item: Fresenius Modified Mixer Motor (for 132 Gallon Dissolution Units) Recalled...

The Issue: Dissolution units and replacement motors units do not provide full thermal...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2015· Fresenius Medical Care Renal Therapies Group, LLC

Recalled Item: Fresenius 132 Gallon Dry Acid Dissolution Unit Recalled by Fresenius Medical...

The Issue: Dissolution units and replacement motors units do not provide full thermal...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2015· Medtronic Vascular, Inc.

Recalled Item: Amphirion Deep OTW PTA Balloon Catheter: Model numbers: US: AMP015020152...

The Issue: Medtronic has discovered that select lots of the Amphirion Deep PTA Balloon...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2015· Otto Bock Healthcare GmbH

Recalled Item: iOS Galileo Application Version 1.1.1 or lower that programs the Recalled by...

The Issue: A software issue can make the foot move into dorsiflexion, unnoticed by the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2015· Innokas Medical Oy

Recalled Item: CARESCAPE VC150 Vital Signs Monitor Monitor vital signs in humans Recalled...

The Issue: Monitor may shut down unintentionally without restarting.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2015· Mercury Enterprises, Inc. dba Mercury Medical

Recalled Item: Mercury Medical Neo-Tee T-Piece Resuscitator and T-Piece Circuit. The...

The Issue: Incorrect use of T-Piece resuscitators will result in complete occlusion of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2015· LeMaitre Vascular, Inc.

Recalled Item: LeMaitre Over-the-Wire Embolectomy Catheter 3F Recalled by LeMaitre...

The Issue: Manufacturing issue that could cause a pinhole in the formed end of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2015· LeMaitre Vascular, Inc.

Recalled Item: LeMaitre NovaSil Silicone Single Lumen Embolectomy Catheter 2F Recalled by...

The Issue: Manufacturing issue that could cause a pinhole in the formed end of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2015· LeMaitre Vascular, Inc.

Recalled Item: LeMaitre NovaSil Silicone Single Lumen Embolectomy Catheter 6F Recalled by...

The Issue: Manufacturing issue that could cause a pinhole in the formed end of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2015· Civco Medical Instruments Co. Inc.

Recalled Item: CIVCO Tracking Bracket Starter Kit Recalled by Civco Medical Instruments Co....

The Issue: Sterility of the product cannot be assured.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2015· Civco Medical Instruments Co. Inc.

Recalled Item: CIVCO Sales Demo Kit. Large Gauge Infiniti Plus Recalled by Civco Medical...

The Issue: Sterility of the product cannot be assured.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2015· LeMaitre Vascular, Inc.

Recalled Item: LeMaitre Over-the-Wire Embolectomy Catheter 3F Recalled by LeMaitre...

The Issue: Manufacturing issue that could cause a pinhole in the formed end of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2015· Civco Medical Instruments Co. Inc.

Recalled Item: CIVCO Needle Guide Starter Kit Recalled by Civco Medical Instruments Co....

The Issue: Sterility of the product cannot be assured.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2015· LeMaitre Vascular, Inc.

Recalled Item: LeMaitre Over-the-Wire Embolectomy Catheter 6F Recalled by LeMaitre...

The Issue: Manufacturing issue that could cause a pinhole in the formed end of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2015· Civco Medical Instruments Co. Inc.

Recalled Item: CIVCO Infiniti Plus Needle Guide Recalled by Civco Medical Instruments Co....

The Issue: Sterility of the product cannot be assured.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2015· LeMaitre Vascular, Inc.

Recalled Item: LeMaitre Over-the-Wire Embolectomy Catheter 5F Plus Recalled by LeMaitre...

The Issue: Manufacturing issue that could cause a pinhole in the formed end of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2015· LeMaitre Vascular, Inc.

Recalled Item: LeMaitre Single Lumen Embolectomy Catheter 4F Recalled by LeMaitre Vascular,...

The Issue: Manufacturing issue that could cause a pinhole in the formed end of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2015· LeMaitre Vascular, Inc.

Recalled Item: LeMaitre Single Lumen Embolectomy Catheter 3F Recalled by LeMaitre Vascular,...

The Issue: Manufacturing issue that could cause a pinhole in the formed end of the...

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

Class II — Potential Health HazardOngoing