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 2730127320 of 30,153 recalls

Medical DeviceJuly 30, 2013· Synthes USA HQ, Inc.

Recalled Item: Synthes 2.4 VA-LCP 2 CLMN VLR DSTL Radius PL 7H Recalled by Synthes USA HQ,...

The Issue: The possibility exists that 2.4 mm VA-LCP 2 column distal radius plates from...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2013· Synthes USA HQ, Inc.

Recalled Item: Synthes Trochanteric Fixation Nail As part of the Synthes Trochanteric...

The Issue: Certain lots of Trochanteric Fixation Nail were distributed to the field...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2013· Synthes USA HQ, Inc.

Recalled Item: Titanium Trochanteric Fixation Nail (TFN)System Intended to treat stable and...

The Issue: Two lots of Titanium Trochanteric Fixation Nail (TFN) System are missing the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2013· Synthes USA HQ, Inc.

Recalled Item: Vertebroplasty Needle Kit 10g Diamond Tip Intended to be used Recalled by...

The Issue: Complaints were received of inconsistencies in the expiration dates shown on...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2013· Synthes USA HQ, Inc.

Recalled Item: Synthes Titanium Cannulated Humeral Nail Intended to aid in the Recalled by...

The Issue: The packaging incorrectly depicts the Synthes Titanium Cannulated Humeral...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2013· Synthes (USA) Products LLC

Recalled Item: Synthes 2.4 mm LC-DCP Plate 6 Holes/51mm Product Usage: Intended Recalled by...

The Issue: A complaint was reported regarding a screw being found in a package labeled...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2013· Siemens Healthcare Diagnostics

Recalled Item: ADVIA Chemistry A1c_3 Calibrators Recalled by Siemens Healthcare Diagnostics...

The Issue: Siemens confirmed that the ADVIA¿ Chemistry Systems HbA1c method exhibits a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2013· Edwards Lifesciences, LLC

Recalled Item: Edwards Lifesciences Anastaflo Intravascular Shunt Recalled by Edwards...

The Issue: Edwards Lifesciences is recalling certain lots of the Anastaflo...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2013· Stryker Craniomaxillofacial Division

Recalled Item: Stryker Part Numbers 79-43903 (3cc) Recalled by Stryker Craniomaxillofacial...

The Issue: Stryker received reports of the desiccant bag in the kit leaking silica gel...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2013· Sarken, Inc.

Recalled Item: SARKEN STAT! Multi-Drug Test Panel Product Usage- Labeled as FOR Recalled...

The Issue: These products are being recalled because they were distributed without...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2013· Sarken, Inc.

Recalled Item: SARKEN STAT! Multi-Drug Test Panel Product Usage- Labeled as FOR Recalled...

The Issue: These products are being recalled because they were distributed without...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2013· GE Healthcare, LLC

Recalled Item: Tec 6 continuous Flow Vaporizer and Tec 6 Plus Anesthesia Recalled by GE...

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

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2013· Sarken, Inc.

Recalled Item: SARKEN STAT! 1- Panel Test Kit-COC Product Usage- Labeled as Recalled by...

The Issue: These products are being recalled because they were distributed without...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2013· Sarken, Inc.

Recalled Item: SARKEN STAT! 1- Panel Test Kit-OPI Product Usage: Labeled as Recalled by...

The Issue: These products are being recalled because they were distributed without...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2013· Sarken, Inc.

Recalled Item: SARKEN STAT! 1- Panel Test Kit-mAMP Product Usage: Labeled as Recalled by...

The Issue: These products are being recalled because they were distributed without...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2013· Sarken, Inc.

Recalled Item: SARKEN STAT! 1- Panel Test Kit-THC Product Usage- Labeled as Recalled by...

The Issue: These products are being recalled because they were distributed without...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2013· ASO, LLC

Recalled Item: Premier Value Wound Closure Adhesive Surgical Tape Strips 30 strips Recalled...

The Issue: This recall has been initiated by Aspen Surgical Products, Inc., due to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2013· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo¿ Advanced Perfusion System 1: 220/240V AC Recalled by Terumo...

The Issue: The operators manual does not fully describe the sequence of expected events...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2013· Carestream Health, Inc.

Recalled Item: DRX Revolution Mobile X-Ray System Recalled by Carestream Health, Inc. Due...

The Issue: During an audit, Carestream discovered a DRX-1 System that captured an image...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2013· Terumo Cardiovascular Systems Corporation

Recalled Item: 220/240V AC Recalled by Terumo Cardiovascular Systems Corporation Due to...

The Issue: TCVS is taking action to update the Operators Manual with the specific...

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

Class II — Potential Health HazardOngoing