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. 2,868 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
2,868 in last 12 months

Showing 50615080 of 30,153 recalls

Medical DeviceDecember 21, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE BLOOD CULTURE KIT Recalled by MEDLINE INDUSTRIES, LP - Northfield...

The Issue: Medline Industries, LP is issuing a recall for specific item(s) and lot(s)...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE BLOOD CULTURE COLLECTION KIT Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: Medline Industries, LP is issuing a recall for specific item(s) and lot(s)...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2023· AMD Medicom Inc.

Recalled Item: HENRY SCHEIN¿ CRITERION¿ ANTI-FOG EARLOOP MASKS LEVEL 3 (BLUE) (item...

The Issue: Level 3 masks were produced on alternate non-validated production equipment...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE BLOOD CULTURE TRAY ADULT Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: Medline Industries, LP is issuing a recall for specific item(s) and lot(s)...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2023· AMD Medicom Inc.

Recalled Item: HENRY SCHEIN¿ CRITERION¿ EARLOOP MASKS LEVEL 3 (BLUE) (item code 570-2448)...

The Issue: Level 3 masks were produced on alternate non-validated production equipment...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE BLOOD CULTURE COLLECTION KIT Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: Medline Industries, LP is issuing a recall for specific item(s) and lot(s)...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2023· CooperSurgical, Inc.

Recalled Item: global Medium Recalled by CooperSurgical, Inc. Due to The firm has become...

The Issue: The firm has become aware of a sudden increase in complaints for three...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2023· Barco N.V.

Recalled Item: Barco MDSC-8527 NXF Recalled by Barco N.V. Due to Barco became aware of a...

The Issue: Barco became aware of a problem with I2C cables in the manufacturing process...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2023· Zyno Medical LLC

Recalled Item: Zyno Medical Z800 Large Volume Infusion Pumps -Intended to provide Recalled...

The Issue: When utlizing the patient query feature on the Zyno Medical Z-800WF pumps...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2023· Acumed LLC

Recalled Item: Acu-Loc and Acu-Loc 2 bone plates Recalled by Acumed LLC Due to Distribution...

The Issue: Distribution without Pre-Market Clearance

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2023· Smiths Medical ASD Inc.

Recalled Item: smiths medical Medfusion Model 4000 syringe pump Recalled by Smiths Medical...

The Issue: Medfusion Model 4000 syringe infusion pumps, with the following software...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 18, 2023· Vortex Surgical Inc.

Recalled Item: Vortex Surgical ACTU8 FORCEPS Recalled by Vortex Surgical Inc. Due to Reason...

The Issue: Reason for the voluntary recall is residue was identified on the two forceps...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2023· St. Jude Medical, Atrial Fibrillation Division, Inc.

Recalled Item: TactiFlex Ablation Sensor Enabled Ablation Catheter Recalled by St. Jude...

The Issue: When the catheters are used with the EnSiteX EP System, the system does not...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2023· Philips North America

Recalled Item: BrightView XCT Recalled by Philips North America Due to Detector may...

The Issue: Detector may unexpectedly fall due to a component failure. If the detector...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 15, 2023· Olympus Corporation of the Americas

Recalled Item: ESG PK CUTTING FORCEPS Recalled by Olympus Corporation of the Americas Due...

The Issue: The jaw may fracture prior to the procedure during the inspection instructed...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2023· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Total immunoglobulin M (IgM total) IVD Recalled by Siemens Healthcare...

The Issue: Potential for a negative bias with quality control (QC) and patient sample...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2023· Hologic, Inc.

Recalled Item: PANTHER FUSION System The Panther System is an Recalled by Hologic, Inc. Due...

The Issue: Due to potential false positive Flu B results when a sample was also...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2023· Philips North America

Recalled Item: ProxiDiagnost upgrade- A Multi-functional general Radiography and...

The Issue: Issue 1: Mixed Images: The Radio Fluoroscopy (RF) viewer may also display a...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2023· Philips North America

Recalled Item: BrightView X Recalled by Philips North America Due to Detector may...

The Issue: Detector may unexpectedly fall due to a component failure. If the detector...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 15, 2023· Philips North America

Recalled Item: BrightView Recalled by Philips North America Due to Detector may...

The Issue: Detector may unexpectedly fall due to a component failure. If the detector...

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

Class I — Serious Health HazardOngoing