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. 2,704 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
2,704 in last 12 months

Showing 1956119580 of 30,153 recalls

Medical DeviceMarch 9, 2017· Centurion Medical Products Corporation

Recalled Item: OPHTHALMIC DRESSING TRAY The Covidien Curity Oval Eye Pads are Recalled by...

The Issue: Centurion Medical Products is recalling Convenience Kits that contain...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2017· Centurion Medical Products Corporation

Recalled Item: OPHTHALMIC DRS TRAY The Covidien Curity Oval Eye Pads are Recalled by...

The Issue: Centurion Medical Products is recalling Convenience Kits that contain...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2017· Centurion Medical Products Corporation

Recalled Item: POST-OP EYE TRAY The Covidien Curity Oval Eye Pads are Recalled by Centurion...

The Issue: Centurion Medical Products is recalling Convenience Kits that contain...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2017· Centurion Medical Products Corporation

Recalled Item: POST-OPERATIVE OPHTHALMIC DRESSING TRAY The Covidien Curity Oval Eye Pads...

The Issue: Centurion Medical Products is recalling Convenience Kits that contain...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2017· Smith & Nephew, Inc.

Recalled Item: D-RAD Recalled by Smith & Nephew, Inc. Due to The expiration dates on the...

The Issue: The expiration dates on the labeling are incorrect, the actual expiration...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2017· Smith & Nephew, Inc.

Recalled Item: D-RAD Recalled by Smith & Nephew, Inc. Due to The expiration dates on the...

The Issue: The expiration dates on the labeling are incorrect, the actual expiration...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2017· Smith & Nephew, Inc.

Recalled Item: Peri-Loc(R) VLP 3.5 MM X 6 MM SELF-TAPPING CORTEX SCREW Recalled by Smith &...

The Issue: The expiration dates on the labeling are incorrect, the actual expiration...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2017· Centurion Medical Products Corporation

Recalled Item: CUSTOM CADAVER KIT The Covidien Curity Oval Eye Pads are Recalled by...

The Issue: Centurion Medical Products is recalling Convenience Kits that contain...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2017· Smith & Nephew, Inc.

Recalled Item: D-RAD Recalled by Smith & Nephew, Inc. Due to The expiration dates on the...

The Issue: The expiration dates on the labeling are incorrect, the actual expiration...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2017· Cincinnati Sub-Zero Products Inc

Recalled Item: Hemotherm CE Recalled by Cincinnati Sub-Zero Products Inc Due to Improperly...

The Issue: Improperly rated fuses were used in the manufacture of the device.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2017· Centurion Medical Products Corporation

Recalled Item: EYE KIT The Covidien Curity Oval Eye Pads are individually Recalled by...

The Issue: Centurion Medical Products is recalling Convenience Kits that contain...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2017· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens ADVIA Centaur BR assay Cat No. 02419937 Recalled by Siemens...

The Issue: Potential for the ADVIA Centaur Syphilis assay to interfere with the BR (CA...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2017· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens ADVIA Centaur BR assay Cat No. 09010686 Recalled by Siemens...

The Issue: Potential for the ADVIA Centaur Syphilis assay to interfere with the BR (CA...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2017· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens ADVIA Centaur BR assay Cat No. 03896216 Recalled by Siemens...

The Issue: Potential for the ADVIA Centaur Syphilis assay to interfere with the BR (CA...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2017· Ortho-Clinical Diagnostics

Recalled Item: enGen (TM) Laboratory Automation Systems using all TCAutomation(TM) Software...

The Issue: Software anomaly; Thermo-Fisher Scientific initially discovered and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2017· Ferno-Washington Inc

Recalled Item: Ferno PROFlexx¿ Model 28Z Chair Cot Recalled by Ferno-Washington Inc Due to...

The Issue: The recall was initiated as a result of the detection of an incorrect nut...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2017· Ulrich Medical USA Inc

Recalled Item: uNion Cervical Plate System Product Usage: The uNion Cervical Plate Recalled...

The Issue: Surgical technique was revised to prevent static plate screws blocking...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2017· Siemens Medical Solutions USA, Inc

Recalled Item: Syngo.x Recalled by Siemens Medical Solutions USA, Inc Due to Software...

The Issue: Software changes now available to address several issues

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2017· Philips Electronics North America Corporation

Recalled Item: Philips IntelliVue MX4O WLAN Patient Wearable Monitor Product: 865352...

The Issue: Philips lntelliVue MX4O WLAN Patient Wearable Monitor may not automatically...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2017· Siemens Medical Solutions USA, Inc

Recalled Item: Syngo.via Recalled by Siemens Medical Solutions USA, Inc Due to Software...

The Issue: Software changes now available to address several issues

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

Class II — Potential Health HazardOngoing