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. 2,100 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
2,100 in last 12 months

Showing 63816400 of 30,153 recalls

Medical DeviceMay 22, 2023· Universal Meditech Inc.

Recalled Item: PrestiBio Ovulation Strips 60 LH Test Strips Recalled by Universal Meditech...

The Issue: Universal Meditech Inc. was violatively distributing PrestiBio" Breastmilk...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2023· Universal Meditech Inc.

Recalled Item: HealthyWiser UriTest" 10 Parameter Reagent Test Strips for Urinalysis...

The Issue: Universal Meditech Inc. was violatively distributing PrestiBio" Breastmilk...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2023· Universal Meditech Inc.

Recalled Item: OMTMO One Step Ovulation (LH) Test Strips Recalled by Universal Meditech...

The Issue: Universal Meditech Inc. was violatively distributing PrestiBio" Breastmilk...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2023· Baxter Healthcare Corporation

Recalled Item: Voalte Patient Safety Recalled by Baxter Healthcare Corporation Due to...

The Issue: Baxter identified a potential risk where the "safety" monitoring and "bed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2023· ARROW INTERNATIONAL Inc.

Recalled Item: ARROW Endurance Extended Dwell Peripheral Catheter System Recalled by ARROW...

The Issue: Potential for catheter separation or leakage

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 19, 2023· Baxter Healthcare Corporation

Recalled Item: NaviCare Patient Safety V3.9.200 to 3.9.600 Recalled by Baxter Healthcare...

The Issue: Baxter identified a potential risk where the "safety" monitoring and "bed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2023· Ascensia Diabetes Care US, Inc.

Recalled Item: Contour¿ next GEN Blood Glucose Monitoring System Recalled by Ascensia...

The Issue: Ascensia Diabetes Care has determined through customer complaints that 580...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2023· Qiagen GmbH

Recalled Item: QIAstat-Dx Respiratory SARS-CoV-2 Panel -US IVD qualitative test intended...

The Issue: Identified a decreased performance reliability rate, Run abortions could...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2023· Qiagen GmbH

Recalled Item: QIAstat-Dx Respiratory SARS-CoV-2 Panel (V1 and V2 Recalled by Qiagen GmbH...

The Issue: Identified a decreased performance reliability rate, Run abortions could...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2023· Olympus Corporation of the Americas

Recalled Item: UroPass Ureteral Access Sheaths Recalled by Olympus Corporation of the...

The Issue: Dilator tips may break in the package and in patients during surgical...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Probe Cover Kits containing sterile Ultrasound Gel Recalled by...

The Issue: Probe covers for use during diagnostic ultrasound procedures may have an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Probe Cover Kits containing sterile Ultrasound Gel Recalled by...

The Issue: Probe covers for use during diagnostic ultrasound procedures may have an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Probe Cover Kits containing sterile Ultrasound Gel Recalled by...

The Issue: Probe covers for use during diagnostic ultrasound procedures may have an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Probe Cover Kits containing sterile Ultrasound Gel Recalled by...

The Issue: Probe covers for use during diagnostic ultrasound procedures may have an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Probe Cover Kits containing sterile Ultrasound Gel Recalled by...

The Issue: Probe covers for use during diagnostic ultrasound procedures may have an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Probe Cover Kits containing sterile Ultrasound Gel Recalled by...

The Issue: Probe covers for use during diagnostic ultrasound procedures may have an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE NON-STERILE PVP SOLUTION Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: Affected product lots were mislabeled as "STERILE PVP SLN" when they should...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE NON-STERILE PVP SOLUTION Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: Affected product lots were mislabeled as "STERILE PVP SLN" when they should...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Probe Cover Kits containing sterile Ultrasound Gel Recalled by...

The Issue: Probe covers for use during diagnostic ultrasound procedures may have an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2023· Baxter Healthcare Corporation

Recalled Item: Allen Advance Chest Support with Pad Recalled by Baxter Healthcare...

The Issue: Potential for the device to crack where the Chest Base Prone support...

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

Class II — Potential Health HazardOngoing