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. 2,506 recalls have been distributed to Delaware in the last 12 months.

48,330 total recalls
2,506 in last 12 months

Showing 1886118880 of 27,373 recalls

Medical DeviceAugust 5, 2016· Riverpoint Medical, LLC

Recalled Item: Polypropylene Surgical Sutures Recalled by Riverpoint Medical, LLC Due to...

The Issue: Polypropylene Surgical Sutures are recalled because the seals may become...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 4, 2016· Beckman Coulter Inc.

Recalled Item: UniCel DxH Slidemaker Stainer Coulter Cellular Analysis System Recalled by...

The Issue: Beckman Coulter is recalling the UniCel DxH Slidemaker Stainer Coulter...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 4, 2016· Terumo Medical Corp

Recalled Item: MISAGO RX Self Expanding Peripheral Stem Recalled by Terumo Medical Corp Due...

The Issue: During recent routine testing, the MISAGO Peripheral Stent was found not to...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista¿ Calcium (CA) Flex¿ reagent cartridge Device Listing No.:...

The Issue: Siemens Healthcare Diagnostics determined that the Dimension Vista Calcium...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2016· C.R. Bard, Inc.

Recalled Item: BARDIA¿ 60cc Piston Irrigation Syringe Recalled by C.R. Bard, Inc. Due to...

The Issue: Package Defect: Products may be at risk for having a slit defect on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2016· LeMaitre Vascular, Inc.

Recalled Item: 1.5 mm HYDRO LeMaitre Valvulotome Recalled by LeMaitre Vascular, Inc. Due to...

The Issue: Wire which deploys the loop may be come detached at the handle causing the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2016· C.R. Bard, Inc.

Recalled Item: BARD¿ 70cc Piston Syringe with Catheter Tip Recalled by C.R. Bard, Inc. Due...

The Issue: Package Defect: Products may be at risk for having a slit defect on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2016· C.R. Bard, Inc.

Recalled Item: BARD¿ Piston Syringe Recalled by C.R. Bard, Inc. Due to Package Defect:...

The Issue: Package Defect: Products may be at risk for having a slit defect on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2016· LeMaitre Vascular, Inc.

Recalled Item: 1.5 mm HYDRO LeMaitre Valvulotome without LeMills Recalled by LeMaitre...

The Issue: Wire which deploys the loop may be come detached at the handle causing the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2016· C.R. Bard, Inc.

Recalled Item: BARD¿ Irrigation Recalled by C.R. Bard, Inc. Due to Package Defect: Products...

The Issue: Package Defect: Products may be at risk for having a slit defect on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2016· LeMaitre Vascular, Inc.

Recalled Item: 1.5 mm HYDRO LeMaitre Valvulotome Recalled by LeMaitre Vascular, Inc. Due to...

The Issue: Wire which deploys the loop may be come detached at the handle causing the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2016· Hologic, Inc

Recalled Item: SureSight Obturator Introducer Localization Systems (ILS) for ATEC in MRI....

The Issue: Tip Breakage at the glue joint between the obturator body and tip

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Syngo Plaza picture archiving and communication system (PAC) (PACS) intended...

The Issue: Siemens is releasing a Customer Advisory Notice to explain meaning of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2016· Alere San Diego, Inc.

Recalled Item: LDX Optical Check Cassettes (OCC) Model Number: 10-228 and 14-535 Recalled...

The Issue: Incorrect expiration date on the magnetic strip that does not match the...

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

Class III — Low RiskOngoing
Medical DeviceAugust 2, 2016· Randox Laboratories Ltd.

Recalled Item: Randox Lipase (Colorimetric) Product Usage: A lipase test system is Recalled...

The Issue: According to the firm carry over was observed when the Lipase test is run...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2016· Bayer Healthcare

Recalled Item: Certegra Workstation used in conjunction with Medrad Stellant CT Injection...

The Issue: CertegraWorkstation when used in conjunction with the Medrad Stellant CT...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Syngo.Plaza VB 10 A Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: Siemens is releasing a Customer Advisory Notice to explain meaning of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2016· Becton Dickinson & Company

Recalled Item: catalog # 405612 BD Spinal Anesthesia Tray 22G x 3.5 Recalled by Becton...

The Issue: A recall was initiated by Hospira, Inc. for several lots of 5% Lidocaine HCI...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2016· Hologic, Inc

Recalled Item: SureSight Obturator Introducer Localization Systems (ILS) for ATEC in MRI....

The Issue: Tip Breakage at the glue joint between the obturator body and tip

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Multix Fusion Stationary X-Ray System Product Usage: The Multix Fusion...

The Issue: Siemens became aware of a potential issue with the patient table for Ysio...

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

Class II — Potential Health HazardOngoing