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. 2,861 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
2,861 in last 12 months

Showing 55215540 of 30,153 recalls

Medical DeviceOctober 11, 2023· Randox Laboratories Ltd.

Recalled Item: RANDOX Total Bilirubin. Recalled by Randox Laboratories Ltd. Due to Randox...

The Issue: Randox has had reports of elevated patient results using Plasma (lithium...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2023· Unomedical A/S

Recalled Item: VariSoft infusion set Recalled by Unomedical A/S Due to The Varisoft...

The Issue: The Varisoft infusion set is used in conjunction with tandem insulin pumps....

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 11, 2023· SunMed Holdings, LLC

Recalled Item: Medline manual resuscitators with integrated manometer Recalled by SunMed...

The Issue: A backwards leak present in the integrated manometer of the patient valve...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2023· SunMed Holdings, LLC

Recalled Item: Ventlab Recalled by SunMed Holdings, LLC Due to A backwards leak present in...

The Issue: A backwards leak present in the integrated manometer of the patient valve...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2023· SunMed Holdings, LLC

Recalled Item: Ventlab Recalled by SunMed Holdings, LLC Due to A backwards leak present in...

The Issue: A backwards leak present in the integrated manometer of the patient valve...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2023· SunMed Holdings, LLC

Recalled Item: Ventlab Recalled by SunMed Holdings, LLC Due to A backwards leak present in...

The Issue: A backwards leak present in the integrated manometer of the patient valve...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2023· SunMed Holdings, LLC

Recalled Item: Ventlab Recalled by SunMed Holdings, LLC Due to A backwards leak present in...

The Issue: A backwards leak present in the integrated manometer of the patient valve...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2023· Becton Dickinson & Company

Recalled Item: BD gravity sets (Product Name Recalled by Becton Dickinson & Company Due to...

The Issue: Affected infusion sets labeled as free of DEHP actually do contain...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2023· SunMed Holdings, LLC

Recalled Item: Ventlab Recalled by SunMed Holdings, LLC Due to A backwards leak present in...

The Issue: A backwards leak present in the integrated manometer of the patient valve...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2023· Becton Dickinson & Company

Recalled Item: BD Extension Sets (Product Name Recalled by Becton Dickinson & Company Due...

The Issue: Affected infusion sets labeled as free of DEHP actually do contain...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2023· SunMed Holdings, LLC

Recalled Item: Ventlab Recalled by SunMed Holdings, LLC Due to A backwards leak present in...

The Issue: A backwards leak present in the integrated manometer of the patient valve...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2023· SunMed Holdings, LLC

Recalled Item: Curaplex manual resuscitators with integrated manometer Recalled by SunMed...

The Issue: A backwards leak present in the integrated manometer of the patient valve...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2023· Unomedical A/S

Recalled Item: VariSoft infusion set Recalled by Unomedical A/S Due to The Varisoft...

The Issue: The Varisoft infusion set is used in conjunction with tandem insulin pumps....

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 11, 2023· Becton Dickinson & Company

Recalled Item: BD Alaris Pump infusion sets (Product Name Recalled by Becton Dickinson &...

The Issue: Affected infusion sets labeled as free of DEHP actually do contain...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2023· Unomedical A/S

Recalled Item: VariSoft infusion set Recalled by Unomedical A/S Due to The Varisoft...

The Issue: The Varisoft infusion set is used in conjunction with tandem insulin pumps....

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 11, 2023· SunMed Holdings, LLC

Recalled Item: Ventlab Recalled by SunMed Holdings, LLC Due to A backwards leak present in...

The Issue: A backwards leak present in the integrated manometer of the patient valve...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2023· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS XT 3400 Chemistry System Product Code 6844458 Running Software...

The Issue: During planned monitoring of data post-release of Software Version 3.8.0 an...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2023· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS 4600 Chemistry System Product Code 6802445 and Product Recalled by...

The Issue: During planned monitoring of data post-release of Software Version 3.8.0 an...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2023· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS XT 7600 Integrated System Product Code 6844461 Running Software...

The Issue: During planned monitoring of data post-release of Software Version 3.8.0 an...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2023· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS 5600 Integrated System Product Code 6802413 and Product Recalled by...

The Issue: During planned monitoring of data post-release of Software Version 3.8.0 an...

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

Class II — Potential Health HazardOngoing