Product Recalls in New York

Product recalls affecting New York — including food, drugs, consumer products, medical devices, and vehicles distributed to New York. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,659 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
2,659 in last 12 months

Showing 2692126940 of 30,153 recalls

Medical DeviceOctober 7, 2013· Medtronic Vascular, Inc.

Recalled Item: Resolute Integrity Zotarolimus-eluting Coronary Stent: Stent ID 3.0 mm...

The Issue: A small number of units in lot number 0006573585 of the Resolute Integrity...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 7, 2013· Mindray DS USA, Inc. dba Mindray North America

Recalled Item: Multi Parameter Patient Monitor (with Arrhythmia Detection and Alarms)...

The Issue: Mindray has identified an issue with V Series Monitor where the V Dock power...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 7, 2013· Smith & Nephew Inc

Recalled Item: GENESIS(R) II Recalled by Smith & Nephew Inc Due to Swapped product....

The Issue: Swapped product. Non-porous tibial base size 5 L was mis-packaged as size 6...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 7, 2013· Baxter Healthcare Corp.

Recalled Item: 1) The HomeChoice automated peritoneal dialysis system. Dataplate located on...

The Issue: In systems with version 10.4 software Initial Drain logic, the device will...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2013· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products COCM Reagent Recalled by Ortho-Clinical...

The Issue: Inaccurate quality control results.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2013· Biomet 3i, LLC

Recalled Item: ENDOBON XENOGRAFT GRANULES 0.5 ML (Bovine bone substitute) Endobon is...

The Issue: Individual pieces of a batch of Biomet's Endobon Xenograft Granules 0.5 ML...

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

Class III — Low RiskOngoing
Medical DeviceOctober 3, 2013· Synthes USA HQ, Inc.

Recalled Item: Synthes 8.5 MM Medullary Reamer Product Usage: An orthopedic manual Recalled...

The Issue: Complaints were received for intraoperative reamer head breakages which can...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2013· Advanced Sterilization Products

Recalled Item: STERITITE Containers: STERITITE Container Kit Recalled by Advanced...

The Issue: Advanced Sterilization Products (ASP) is recalling the SteriTite containers...

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

Class III — Low RiskOngoing
Medical DeviceOctober 3, 2013· Synthes USA HQ, Inc.

Recalled Item: Synthes Spiked Washers 13.5/6.5 Spiked Washers 13.5/6.5 are intended to...

The Issue: During a retrospective assessment, Spiked Washers 13.5/6.5 were discovered...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2013· Synthes USA HQ, Inc.

Recalled Item: Synthes Titanium Trochanteric Fixation Nail (TFN)-Helical Blade Synthes...

The Issue: A potential exists for non conforming Synthes Titanium Trochanteric Fixation...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2013· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Recalled by Stryker Instruments Div. of Stryker Corporation Due to It was...

The Issue: It was discovered that the silicone potting failed to properly cure after...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2013· Beckman Coulter Inc.

Recalled Item: Access Immunoassay Systems Reaction Vessels. The Access Immunoassay System...

The Issue: Beckman Coulter is initiating a recall for the Access Immunoassay Systems...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2013· Intuitive Surgical, Inc.

Recalled Item: Single Site Curved Needed Driver Intuitive Surgical Recalled by Intuitive...

The Issue: A limited number of FDA-cleared instruments for da Vinci Single Site use,...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2013· Intuitive Surgical, Inc.

Recalled Item: Single Site Bipolar Maryland Forceps Intuitive Surgical Recalled by...

The Issue: A limited number of FDA-cleared instruments for da Vinci Single Site use,...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2013· Nipro Diagnostics, Inc.

Recalled Item: MooreMedical Supporting Health & Care...MooreBrand Blood Glucose Monitor for...

The Issue: Manufactured with an incorrect factory set unit of measure.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2013· Nipro Diagnostics, Inc.

Recalled Item: MooreMedical Supporting Health & Care...MooreBrand Blood Glucose Monitor for...

The Issue: Manufactured with an incorrect factory set unit of measure.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2013· GE Healthcare, LLC

Recalled Item: GE Healthcare - Giraffe Warmer Recalled by GE Healthcare, LLC Due to Oxygen...

The Issue: Oxygen and air wall inlet fittings on the back panel of the resuscitation...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 1, 2013· Toshiba American Medical Systems Inc

Recalled Item: TSX-101A Aquilion 32/64 ONE Computed Tomography X-Ray System Recalled by...

The Issue: Toshiba intitiated this recall because their investigation revealed that due...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2013· GE Healthcare, LLC

Recalled Item: GE Healthcare - Giraffe and Panda Bag and Mask Resuscitation System Recalled...

The Issue: Oxygen and air wall inlet fittings on the back panel of the resuscitation...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 1, 2013· GE Healthcare, LLC

Recalled Item: GE Healthcare - Giraffe¿ and Panda¿ iRes Infant Warmer Product Recalled by...

The Issue: Oxygen and air wall inlet fittings on the back panel of the resuscitation...

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

Class I — Serious Health HazardOngoing