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 2704127060 of 27,373 recalls

Medical DeviceJanuary 26, 2012· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker T2 Arthrodesis Nailing System. Manufacturer: Stryker Trauma GmbH...

The Issue: Stryker has become aware that there exists a potential for breach of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 24, 2012· Exactech, Inc.

Recalled Item: ***NOVATION MODULAR DRILL BIT LENGTH: 40mm Recalled by Exactech, Inc. Due to...

The Issue: Exactech Inc. of Gainesville, FL is recalling their Novation Modular Drill...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 24, 2012· Exactech, Inc.

Recalled Item: ***NOVATION MODULAR DRILL BIT LENGTH: 30mm Recalled by Exactech, Inc. Due to...

The Issue: Exactech Inc. of Gainesville, FL is recalling their Novation Modular Drill...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 24, 2012· Exactech, Inc.

Recalled Item: ***NOVATION MODULAR DRILL BIT LENGTH: 40mm Recalled by Exactech, Inc. Due to...

The Issue: Exactech Inc. of Gainesville, FL is recalling their Novation Modular Drill...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 24, 2012· Exactech, Inc.

Recalled Item: ***NOVATION MODULAR DRILL BIT LENGTH: 20mm Recalled by Exactech, Inc. Due to...

The Issue: Exactech Inc. of Gainesville, FL is recalling their Novation Modular Drill...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 24, 2012· Exactech, Inc.

Recalled Item: ***NOVATION MODULAR DRILL BIT LENGTH: 30mm Recalled by Exactech, Inc. Due to...

The Issue: Exactech Inc. of Gainesville, FL is recalling their Novation Modular Drill...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 24, 2012· Exactech, Inc.

Recalled Item: ***NOVATION MODULAR DRILL BIT LENGTH: 20mm Recalled by Exactech, Inc. Due to...

The Issue: Exactech Inc. of Gainesville, FL is recalling their Novation Modular Drill...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 23, 2012· GE Healthcare, LLC

Recalled Item: VMX Recalled by GE Healthcare, LLC Due to GE Healthcare has become aware of...

The Issue: GE Healthcare has become aware of an issue associated with the base casting...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2012· Beckman Coulter Inc.

Recalled Item: COULTER PrepPlus Recalled by Beckman Coulter Inc. Due to The recall was...

The Issue: The recall was initiated because Beckman Coulter has confirmed that the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 19, 2012· Nihon Kohden America Inc

Recalled Item: MEE-1000A Neuromaster Recalled by Nihon Kohden America Inc Due to The...

The Issue: The MEE-1000A Neuromaster had defective printed circuit boards (PCBs). Gas...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 13, 2012· Stryker Spine

Recalled Item: Stryker AVS Navigator Trials 6mm-15mm Manufactured by: Stryker Spine SAS...

The Issue: Beginning in February 2011, Stryker Spine began receiving reports related to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2012· Vital Scientific N.V.

Recalled Item: V-Twin Recalled by Vital Scientific N.V. Due to The action was initiated due...

The Issue: The action was initiated due power supply failure. During a power supply...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2012· Vital Scientific N.V.

Recalled Item: Selectra ProS Analyzer Recalled by Vital Scientific N.V. Due to The action...

The Issue: The action was initiated due power supply failure. During a power supply...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2012· Vital Scientific N.V.

Recalled Item: Viva-E Recalled by Vital Scientific N.V. Due to The action was initiated due...

The Issue: The action was initiated due power supply failure. During a power supply...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2012· Vital Scientific N.V.

Recalled Item: Viva - JR Recalled by Vital Scientific N.V. Due to The action was initiated...

The Issue: The action was initiated due power supply failure. During a power supply...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2012· Vital Scientific N.V.

Recalled Item: Selectra ProM Analyzer Recalled by Vital Scientific N.V. Due to The action...

The Issue: The action was initiated due power supply failure. During a power supply...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2012· The Anspach Effort, Inc.

Recalled Item: "***Electric Systems Foot Control with Direction and Irrigation***Rx...

The Issue: The Anspach Effort, Inc. in Palm Beach Gardens, FL is recalling the foot...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2012· The Anspach Effort, Inc.

Recalled Item: "***Electric Systems Foot Control****Rx Only***" Product Usage: Cutting and...

The Issue: The Anspach Effort, Inc. in Palm Beach Gardens, FL is recalling the foot...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2012· The Anspach Effort, Inc.

Recalled Item: "***Electric Systems Foot Control with Direction Only***Rx Only***" Product...

The Issue: The Anspach Effort, Inc. in Palm Beach Gardens, FL is recalling the foot...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2012· Cook Ireland Ltd.

Recalled Item: Zilver 518 Vascular Self Expanding Stent The Zilver Vascular Stent Recalled...

The Issue: Cook Ireland received a product complaint from Japan on December 22nd, 2011....

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

Class II — Potential Health HazardOngoing