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. 2,673 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
2,673 in last 12 months

Showing 2398124000 of 30,153 recalls

Medical DeviceMarch 10, 2015· Microtek Medical Inc

Recalled Item: LAPAROSCOPIC TUBING SET Recalled by Microtek Medical Inc Due to This recall...

The Issue: This recall is being conducted because a cohesive band used to package the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2015· Microtek Medical Inc

Recalled Item: TUBING 7/8' X 10' Recalled by Microtek Medical Inc Due to This recall is...

The Issue: This recall is being conducted because a cohesive band used to package the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2015· Microtek Medical Inc

Recalled Item: TUBING SET 7/8" X 6' WITH 1/4" x 24" TUBING Recalled by Microtek Medical Inc...

The Issue: This recall is being conducted because a cohesive band used to package the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2015· Microtek Medical Inc

Recalled Item: FREEDOMAIRE(R) MOTOR MODULE Recalled by Microtek Medical Inc Due to This...

The Issue: This recall is being conducted because a cohesive band used to package the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2015· Microtek Medical Inc

Recalled Item: Smoke Evacuation Tubing Set for Coherent CPG Handpiece Recalled by Microtek...

The Issue: This recall is being conducted because a cohesive band used to package the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2015· Microtek Medical Inc

Recalled Item: FREEDOMAIRE(R) HELMET WITH MOTOR MODULE Recalled by Microtek Medical Inc Due...

The Issue: This recall is being conducted because a cohesive band used to package the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2015· Microtek Medical Inc

Recalled Item: FREEDOMAIRE(R) HELMET SYSTEM WITH BELT Recalled by Microtek Medical Inc Due...

The Issue: This recall is being conducted because a cohesive band used to package the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2015· Microtek Medical Inc

Recalled Item: FREEDOMAIRE(R) HELMET SYSTEM WITH SUPER POWER PAK BATTERY Recalled by...

The Issue: This recall is being conducted because a cohesive band used to package the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2015· Microtek Medical Inc

Recalled Item: (S) TUBE SET 1/4" X 10' (0.64 cm X 304.8 cm) with 7/8" (2.22 cm) Adaptor...

The Issue: This recall is being conducted because a cohesive band used to package the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2015· Microtek Medical Inc

Recalled Item: INTEGRAL WAND W/TUBING Recalled by Microtek Medical Inc Due to This recall...

The Issue: This recall is being conducted because a cohesive band used to package the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2015· Microtek Medical Inc

Recalled Item: VACUUM TUBING 7/8" X 6' (2.22cm X 182.88cm) Recalled by Microtek Medical Inc...

The Issue: This recall is being conducted because a cohesive band used to package the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2015· Microtek Medical Inc

Recalled Item: VACUUM TUBING 7/8" X 6' (2.22cm X 182.88cm) Recalled by Microtek Medical Inc...

The Issue: This recall is being conducted because a cohesive band used to package the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2015· US Endoscopy Group Inc

Recalled Item: Talon Grasping Device Recalled by US Endoscopy Group Inc Due to A wire...

The Issue: A wire component on the distal grasping assembly of the device became detached..

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2015· Microtek Medical Inc

Recalled Item: LASER RESISTANT WAND - STERILE Recalled by Microtek Medical Inc Due to This...

The Issue: This recall is being conducted because a cohesive band used to package the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2015· Zimmer, Inc.

Recalled Item: Brand Name: Persona¿ Anterior Sizer with Locking Boom The Recalled by...

The Issue: Zimmer, Inc is voluntarily recalling 22 lots of Persona¿ Anterior Sizer with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2015· Nobel Biocare Usa Llc

Recalled Item: NobelReplace CC PMC NP 3.5x11.5mm Recalled by Nobel Biocare Usa Llc Due to A...

The Issue: A material used in the packaging of the dental implants may impart a sticky...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2015· Specialty Appliance Works, Inc.

Recalled Item: TS ROC Crown Component 4UR (5/pk) Recalled by Specialty Appliance Works,...

The Issue: The Universal Nut, a component of the orthodontic Herbst Appliance was made...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2015· Specialty Appliance Works, Inc.

Recalled Item: Specialty MiniScope Mech. Set Size 18 Recalled by Specialty Appliance Works,...

The Issue: The Universal Nut, a component of the orthodontic Herbst Appliance was made...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2015· Specialty Appliance Works, Inc.

Recalled Item: TS Herbst Nuts with Backing (10/pk) and TS Herbst Nuts Recalled by Specialty...

The Issue: The Universal Nut, a component of the orthodontic Herbst Appliance was made...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2015· Specialty Appliance Works, Inc.

Recalled Item: MiniScope Hst ROC Crown 15 Patient Kit Recalled by Specialty Appliance...

The Issue: The Universal Nut, a component of the orthodontic Herbst Appliance was made...

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

Class II — Potential Health HazardOngoing