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. 2,474 recalls have been distributed to Delaware in the last 12 months.

48,330 total recalls
2,474 in last 12 months

Showing 2254122560 of 27,373 recalls

Medical DeviceOctober 23, 2014· Remel Inc

Recalled Item: Oxoid Legionella Latex Test Recalled by Remel Inc Due to A reagent within...

The Issue: A reagent within the test may return false negative results.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2014· TEM Systems Inc

Recalled Item: ROTROL P Control for ROTEM delta Thromboelastometry System Recalled by TEM...

The Issue: Some of vials were found to be partially filled.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2014· Data Innovations, LLC

Recalled Item: JResultNet drivers using ASTM coding language. Calculator/data processing...

The Issue: Software issue resulting in the results of one patient potentially being...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2014· Centurion Medical Products Corporation

Recalled Item: Nerve Block Tray (Nerve Block convenience kit) Recalled by Centurion Medical...

The Issue: According to the recall notice received from Hospira, the recall was...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2014· Centurion Medical Products Corporation

Recalled Item: Diagnostic Imaging Tray (General Surgery convenience kit) Recalled by...

The Issue: According to the recall notice received from Hospira, the recall was...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2014· Centurion Medical Products Corporation

Recalled Item: Pacemaker Tray (Cardiovascular Surgical Instruments convenience kit)...

The Issue: According to the recall notice received from Hospira, the recall was...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2014· Centurion Medical Products Corporation

Recalled Item: Chest Tube Tray (Cardiovascular Surgical Instruments convenience kit)...

The Issue: According to the recall notice received from Hospira, the recall was...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2014· Medtest Holdings, Inc.

Recalled Item: MedTest DX Assayed Human Multi Sera Control Level 1 (HNC200) Recalled by...

The Issue: MedTest DX Assayed Human Multi Sera Control Level 1 (HNC200) and Level 2...

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

Class III — Low RiskOngoing
Medical DeviceOctober 21, 2014· Gyrus Acmi, Incorporated

Recalled Item: Gyrus ACMI Disposable Falope-Ring Band Applicator Kits. and Recalled by...

The Issue: All packages of Falope Ring Band Applicator kits are being recalled due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2014· Microgenics Corporation

Recalled Item: MAS CardioImmune XL Cardiac Marker Control Recalled by Microgenics...

The Issue: MAS CardioImmune XL, level 1 (lot CXL16011), is showing vial-to-vial...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2014· Pfm Medical Inc

Recalled Item: Rapid Centesis Catheter Recalled by Pfm Medical Inc Due to PFM Medical is...

The Issue: PFM Medical is recalling catheters and other medical devices because they...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2014· Pfm Medical Inc

Recalled Item: ASEPT 2000 ml Drainage Bag Recalled by Pfm Medical Inc Due to PFM Medical is...

The Issue: PFM Medical is recalling catheters and other medical devices because they...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2014· Pfm Medical Inc

Recalled Item: ASEPT Peritoneal Drainage System Recalled by Pfm Medical Inc Due to PFM...

The Issue: PFM Medical is recalling catheters and other medical devices because they...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2014· Pfm Medical Inc

Recalled Item: ASEPT 600 ml Drainage Kit Recalled by Pfm Medical Inc Due to PFM Medical is...

The Issue: PFM Medical is recalling catheters and other medical devices because they...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2014· Pfm Medical Inc

Recalled Item: Thoracentesis & Paracentesis Procedure Tray Recalled by Pfm Medical Inc Due...

The Issue: PFM Medical is recalling catheters and other medical devices because they...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2014· Pfm Medical Inc

Recalled Item: ASEPT Pleural Drainage System Recalled by Pfm Medical Inc Due to PFM Medical...

The Issue: PFM Medical is recalling catheters and other medical devices because they...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2014· Pfm Medical Inc

Recalled Item: Micro Introducer Kit Recalled by Pfm Medical Inc Due to PFM Medical is...

The Issue: PFM Medical is recalling catheters and other medical devices because they...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2014· Pfm Medical Inc

Recalled Item: 6F x 60 cm Dual Lumen CT PICC Recalled by Pfm Medical Inc Due to PFM Medical...

The Issue: PFM Medical is recalling catheters and other medical devices because they...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2014· Pfm Medical Inc

Recalled Item: Veta Peritoneal Catheter Kit Recalled by Pfm Medical Inc Due to PFM Medical...

The Issue: PFM Medical is recalling catheters and other medical devices because they...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2014· Diamedix Corporation

Recalled Item: Diamedix Is-Mumps IgG Test Kit Diamedix Is-Mumps IgG Test Kit Recalled by...

The Issue: A gel-like substance was found in kit component, sample diluent , that could...

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

Class II — Potential Health HazardOngoing