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. 1,215 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
1,215 in last 12 months

Showing 661–680 of 30,153 recalls

Medical DeviceOctober 31, 2025· Philips North America Llc

Recalled Item: IntelliVue Patient Monitor MX600. Product Number: 865242. Recalled by...

The Issue: Potential issue where the IntelliVue monitors did not alarm.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2025· Philips North America Llc

Recalled Item: IntelliVue Multi-Measurement Module X3. Product Number: 867030. Recalled by...

The Issue: Potential issue where the IntelliVue monitors did not alarm.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2025· Philips North America Llc

Recalled Item: IntelliVue Patient Monitor MX450. Product Number: 866062. Recalled by...

The Issue: Potential issue where the IntelliVue monitors did not alarm.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2025· Philips North America Llc

Recalled Item: IntelliVue Patient Monitor MX400. Product Number: 866060. Recalled by...

The Issue: Potential issue where the IntelliVue monitors did not alarm.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 30, 2025· Cepheid

Recalled Item: Brand Name: Xpert¿ BCR-ABL Ultra Model/Catalog Number: GXBCRABL-US-10...

The Issue: Invitro diagnostic test kits with specimens that have elevated white blood...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 30, 2025· Cepheid

Recalled Item: Brand Name: Xpert¿ BCR-ABL Ultra Model/Catalog Number: GXBCRABL-10 Recalled...

The Issue: Invitro diagnostic test kits with specimens that have elevated white blood...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 29, 2025· Medicrea International

Recalled Item: Medicrea Recalled by Medicrea International Due to Due to complaints,...

The Issue: Due to complaints, orthopedic rotation tool handle may untread from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 29, 2025· Medicrea International

Recalled Item: Medicrea Recalled by Medicrea International Due to Due to complaints,...

The Issue: Due to complaints, orthopedic rotation tool handle may untread from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 29, 2025· Medtronic, Inc.

Recalled Item: Aurora EV-ICD and Clinical EV-ICD Recalled by Medtronic, Inc. Due to There...

The Issue: There is a potential for delayed time to high-voltage (HV) therapy should a...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 29, 2025· Philips North America Llc

Recalled Item: Incisive CT Recalled by Philips North America Llc Due to If the screws of...

The Issue: If the screws of tube heat exchanger on the rotating scanner are not...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 29, 2025· Philips North America Llc

Recalled Item: CT 5300 Recalled by Philips North America Llc Due to If the screws of tube...

The Issue: If the screws of tube heat exchanger on the rotating scanner are not...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 29, 2025· Copan Italia

Recalled Item: 1ml of DTT in liquid phase Recalled by Copan Italia Due to Treatment reagent...

The Issue: Treatment reagent functionality in respiratory specimens fluidification...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 29, 2025· Copan Italia

Recalled Item: 1ml of DTT in liquid phase Recalled by Copan Italia Due to Treatment reagent...

The Issue: Treatment reagent functionality in respiratory specimens liquification...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 28, 2025· Illumina, Inc.

Recalled Item: Reagent Kits/ containing flow cells Recalled by Illumina, Inc. Due to An...

The Issue: An instrument intended for sequencing DNA libraries with in vitro diagnostic...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 28, 2025· Baxter Healthcare Corporation

Recalled Item: Welch Allyn INF BAG Recalled by Baxter Healthcare Corporation Due to...

The Issue: Replacement bladder kit for the Welch Allyn two-piece reusable blood...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 27, 2025· Nipro Medical Corporation

Recalled Item: Hemodialysis System Recalled by Nipro Medical Corporation Due to Screw may...

The Issue: Screw may loosen or fallout of Hemodialysis system

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 27, 2025· Medline Industries, LP

Recalled Item: MEDLINE PERFUSION SYRINGE Recalled by Medline Industries, LP Due to Medline...

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 DeviceOctober 24, 2025· Edan Diagnostics

Recalled Item: Brand Name: EDAN Product Name: Patient Monitor Model/Catalog Number: iM20...

The Issue: As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2025· Edan Diagnostics

Recalled Item: Brand Name: EDAN Product Name: Patient Monitor Model/Catalog Number: iM50...

The Issue: As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2025· Edan Diagnostics

Recalled Item: Brand Name: EDAN Product Name: Fetal & Maternal Monitor Model/Catalog...

The Issue: As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA...

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

Class II — Potential Health HazardOngoing