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. 2,748 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
2,748 in last 12 months

Showing 1756117580 of 30,153 recalls

Medical DeviceJanuary 2, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: IMMULITE ¿ /IMMULITE ¿ 1000 BR-MA (CA15-3) Recalled by Siemens Healthcare...

The Issue: Concentrations for the level of biotin that does not interfere is not...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: IMMULITE ¿ /IMMULITE ¿ 1000 OM-MA (CA125) Recalled by Siemens Healthcare...

The Issue: Concentrations for the level of biotin that does not interfere is not...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Centaur¿ DHEA-SO4 Recalled by Siemens Healthcare Diagnostics, Inc. Due...

The Issue: The concentrations for biotin listed in the non-interfering substances...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: IMMULITE ¿ 2000/IMMULITE ¿ 2000 XPi Anti HBc Recalled by Siemens Healthcare...

The Issue: Concentrations for the level of biotin that does not interfere is not...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2018· Stryker Sustainability Solutions

Recalled Item: Stryker Sustainability Solutions Reprocessed BW Lasso 2515 NAV eco Variable...

The Issue: An EEPROM chip error code may occur when the catheters are used with CARTO...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2018· Stryker Sustainability Solutions

Recalled Item: Stryker Sustainability Solutions Reprocessed BW Lasso 2515 NAV eco Variable...

The Issue: An EEPROM chip error code may occur when the catheters are used with CARTO...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 28, 2017· Bard Access Systems Inc.

Recalled Item: PowerPICC Provena Catheters Recalled by Bard Access Systems Inc. Due to...

The Issue: Possible leaks on the 3 Fr. Single lumen and 4 Fr. Dual lumen PowerPICC...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 27, 2017· Ormco/Sybronendo

Recalled Item: Elements Obturation Unit (EOU) used with respective Buchanan Heat Pluggers...

The Issue: Buchanan Heat Pluggers will possibly overheat while used with the Elements...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 27, 2017· Mako Surgical Corporation

Recalled Item: Makoplasty RIO Standard System Recalled by Mako Surgical Corporation Due to...

The Issue: Communication-connection error.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2017· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: LATARJET EXPERIENCE Sharp Curved Ostetome Product Usage: The Latarjet...

The Issue: Reports of product loosening or coming unscrewed from the handle.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2017· Howmedica Osteonics Corp.

Recalled Item: Custom Made Implant System with Minimum Invasive Grower (MIG) component...

The Issue: From March 2007 to October 2014, product did not contain updated...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2017· W & H DentalWerk Burmoos GMBH - Site 1

Recalled Item: Foot Controls Model: S-N1 and S-N2 Product Usage: Variable foot Recalled by...

The Issue: During continuous postmarket surveillance activities, we have noticed a...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2017· DePuy Orthopaedics, Inc.

Recalled Item: (1) Sigma HP Cemented Trochlea Size 1 Narrow Left Recalled by DePuy...

The Issue: The SIGMA¿ HP PFJ Cemented Trochlear Implants, a standalone component of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2017· Zimmer Biomet, Inc.

Recalled Item: ACE Trochanteric Nail System STER TROC END CAP STER TROC Recalled by Zimmer...

The Issue: Zimmer Biomet is conducting a medical device recall for the ACE Trochanteric...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2017· Zimmer Biomet, Inc.

Recalled Item: ACE Trochanteric Nail System ATN AR SCREW 60MM STERILE ATN Recalled by...

The Issue: Zimmer Biomet is conducting a medical device recall for the ACE Trochanteric...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2017· Zimmer Biomet, Inc.

Recalled Item: ACE Trochanteric Nail System ATN LAG SCREW 60MM STERILE ATN Recalled by...

The Issue: Zimmer Biomet is conducting a medical device recall for the ACE Trochanteric...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2017· Zimmer Biomet, Inc.

Recalled Item: ACE Trochanteric Nail System TROCH NAIL ST 13X180 125DG STRL Recalled by...

The Issue: Zimmer Biomet is conducting a medical device recall for the ACE Trochanteric...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2017· Zimmer Biomet, Inc.

Recalled Item: ACE Trochanteric Nail System STER TROC NAIL 180X13X140 STER TROC Recalled by...

The Issue: Zimmer Biomet is conducting a medical device recall for the ACE Trochanteric...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2017· Zimmer Biomet, Inc.

Recalled Item: ACE Trochanteric Nail System STER TROC NAIL 125 DEG X Recalled by Zimmer...

The Issue: Zimmer Biomet is conducting a medical device recall for the ACE Trochanteric...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2017· Boston Scientific Corporation

Recalled Item: SpyScope DS Access and Delivery diagnostic biliary catheter Recalled by...

The Issue: Certain lots of devices may have the working channel sleeve protruding from...

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

Class II — Potential Health HazardOngoing