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. 2,846 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
2,846 in last 12 months

Showing 73217340 of 30,153 recalls

Medical DeviceDecember 7, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Surgical convenience kits labeled as: CENTURION MEDICAL PRODUCTS L & D TRAY...

The Issue: The recall is due to the perforated bag not allowing for outside of the kit...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· Philips Respironics, Inc.

Recalled Item: Philips Trilogy 200 Ventilator Recalled by Philips Respironics, Inc. Due to...

The Issue: The replacement silicone sound abatement foam installed into some Trilogy...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 7, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Surgical convenience kits labeled as: MEDLINE PAIN TRAY Recalled by MEDLINE...

The Issue: The recall is due to the perforated bag not allowing for outside of the kit...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Surgical convenience kits labeled as: MEDLINE CABG PACK Recalled by MEDLINE...

The Issue: The recall is due to the perforated bag not allowing for outside of the kit...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Surgical convenience kits labeled as: CENTURION MEDICAL PRODUCTS NEONATAL...

The Issue: The recall is due to the perforated bag not allowing for outside of the kit...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· Johnson & Johnson Surgical Vision, Inc.

Recalled Item: FUSION Dual Pump Packs Recalled by Johnson & Johnson Surgical Vision, Inc....

The Issue: Weld protrusion/physical gap between the housing and phaco pack cover, may...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Surgical convenience kits labeled as: MEDLINE PREP TRAY Recalled by MEDLINE...

The Issue: The recall is due to the perforated bag not allowing for outside of the kit...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Surgical convenience kits labeled as: MEDLINE PERF. ASSOC. CUT DOWN TRAY...

The Issue: The recall is due to the perforated bag not allowing for outside of the kit...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· Johnson & Johnson Surgical Vision, Inc.

Recalled Item: Veritas Advanced Infusion Packs Recalled by Johnson & Johnson Surgical...

The Issue: Weld protrusion/physical gap between the housing and phaco pack cover, may...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Surgical convenience kits labeled as: MEDLINE BREAST BIOPSY KIT Recalled by...

The Issue: The recall is due to the perforated bag not allowing for outside of the kit...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Surgical convenience kits labeled as: MEDLINE ARM/MINOR DRAPE CSTM Recalled...

The Issue: The recall is due to the perforated bag not allowing for outside of the kit...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· Johnson & Johnson Surgical Vision, Inc.

Recalled Item: Single-Use Packs Recalled by Johnson & Johnson Surgical Vision, Inc. Due to...

The Issue: Weld protrusion/physical gap between the housing and phaco pack cover, may...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· The Anspach Effort, Inc.

Recalled Item: 6.5 cm Adult Craniotome Recalled by The Anspach Effort, Inc. Due to Ball...

The Issue: Ball bearings in the CRANI-A (ANSPACH Power Tools Adult Craniotome...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· The Anspach Effort, Inc.

Recalled Item: 6.5 cm Adult Rotating Craniotome Attachment. Use with XMax¿ Recalled by The...

The Issue: Ball bearings in the CRANI-A (ANSPACH Power Tools Adult Craniotome...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· The Anspach Effort, Inc.

Recalled Item: 7.5 cm Large Craniotome Attachment Use with XMax¿ Recalled by The Anspach...

The Issue: Ball bearings in the CRANI-A (ANSPACH Power Tools Adult Craniotome...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· The Anspach Effort, Inc.

Recalled Item: Pediatric Craniotome Recalled by The Anspach Effort, Inc. Due to Ball...

The Issue: Ball bearings in the CRANI-A (ANSPACH Power Tools Adult Craniotome...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· Philips Respironics, Inc.

Recalled Item: Philips Trilogy 100 Ventilator Recalled by Philips Respironics, Inc. Due to...

The Issue: The replacement silicone sound abatement foam installed into some Trilogy...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 7, 2022· Siemens Healthcare Diagnostics, Inc.

Recalled Item: IMMULITE 2000 Thyroglobulin (OUS). For in vitro diagnostic use with Recalled...

The Issue: Potential for Functional Sensitivity to not meet Instructions For Use (IFU)...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Surgical convenience kits labeled as: a) MEDLINE PERF. ASSOC. CUT DOWN TRAY...

The Issue: The recall is due to the perforated bag not allowing for outside of the kit...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Surgical convenience kits labeled as: MEDLINE SHOULDER SUSPENSION I-LF...

The Issue: The recall is due to the perforated bag not allowing for outside of the kit...

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

Class II — Potential Health HazardOngoing