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. 1,185 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
1,185 in last 12 months

Showing 4441–4460 of 30,153 recalls

Medical DeviceMarch 21, 2024· SonarMed Inc

Recalled Item: AW-S030 NEO SONARMED SENSOR 3.0MM. Used in conjunction with SonarMed...

The Issue: The failure to detect the partial obstruction in a 2.5mm sensor.

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 21, 2024· SonarMed Inc

Recalled Item: AW-S025 NEO SONARMED SENSOR 2.5MM. Used in conjunction with SonarMed...

The Issue: The failure to detect the partial obstruction in a 2.5mm sensor.

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 20, 2024· Baxter Healthcare Corporation

Recalled Item: Baxter Spectrum IQ Infusion Pump Recalled by Baxter Healthcare Corporation...

The Issue: One device was improperly performed testing prior to release from a Service...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2024· Ontact Inc

Recalled Item: 24K Premium Lense Recalled by Ontact Inc Due to Contact lenses recalled due...

The Issue: Contact lenses recalled due to potential bacterial contamination.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2024· Zimmer, Inc.

Recalled Item: ZPLP Distal Lateral Fibular Plate Recalled by Zimmer, Inc. Due to Thread...

The Issue: Thread form issue for the locking holes in that the locking screws may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2024· Zimmer, Inc.

Recalled Item: ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular...

The Issue: Thread form issue for the locking holes in that the locking screws may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2024· Zimmer, Inc.

Recalled Item: ZPLP Distal Lateral Fibular Plate Recalled by Zimmer, Inc. Due to Thread...

The Issue: Thread form issue for the locking holes in that the locking screws may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2024· Zimmer, Inc.

Recalled Item: ZPLP Distal Lateral Fibular Plate Recalled by Zimmer, Inc. Due to Thread...

The Issue: Thread form issue for the locking holes in that the locking screws may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2024· Zimmer, Inc.

Recalled Item: ZPLP(Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate...

The Issue: Thread form issue for the locking holes in that the locking screws may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2024· Draeger Medical, Inc.

Recalled Item: Dr¿ger Perseus A500 Anesthesia Workstation Recalled by Draeger Medical, Inc....

The Issue: Unexpected shutdown while operating on battery power.

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 20, 2024· Zimmer, Inc.

Recalled Item: ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular...

The Issue: Thread form issue for the locking holes in that the locking screws may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2024· Zimmer, Inc.

Recalled Item: ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular...

The Issue: Thread form issue for the locking holes in that the locking screws may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2024· Abbott Molecular, Inc.

Recalled Item: Alinity m System Recalled by Abbott Molecular, Inc. Due to The Alinity m...

The Issue: The Alinity m System camera detects whether tubes are "capped." If the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2024· Zimmer, Inc.

Recalled Item: ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular...

The Issue: Thread form issue for the locking holes in that the locking screws may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2024· Zimmer, Inc.

Recalled Item: ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular...

The Issue: Thread form issue for the locking holes in that the locking screws may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2024· Zimmer, Inc.

Recalled Item: ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular...

The Issue: Thread form issue for the locking holes in that the locking screws may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2024· Zimmer, Inc.

Recalled Item: ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular...

The Issue: Thread form issue for the locking holes in that the locking screws may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2024· Zimmer, Inc.

Recalled Item: ZPLP Distal Lateral Fibular Plate Recalled by Zimmer, Inc. Due to Thread...

The Issue: Thread form issue for the locking holes in that the locking screws may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2024· Zimmer, Inc.

Recalled Item: ZPLP Distal Lateral Fibular Plate Recalled by Zimmer, Inc. Due to Thread...

The Issue: Thread form issue for the locking holes in that the locking screws may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2024· Zimmer, Inc.

Recalled Item: ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular...

The Issue: Thread form issue for the locking holes in that the locking screws may not...

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

Class II — Potential Health HazardOngoing