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. 971 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
971 in last 12 months

Showing 48281–48300 of 55,896 recalls

Medical DeviceMarch 11, 2014· Teleflex Medical

Recalled Item: 5/10/12 Weck¿ Vista" Universal Balloon Open Access Port  Standard Length...

The Issue: Complaints were received of leakage of insufflation gas through the device,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2014· Teleflex Medical

Recalled Item: 5/10 mm Weck¿ Recalled by Teleflex Medical Due to Complaints were received...

The Issue: Complaints were received of leakage of insufflation gas through the device,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2014· Teleflex Medical

Recalled Item: Sutures Recalled by Teleflex Medical Due to The products are being recalled...

The Issue: The products are being recalled because they did not meet minimum needle...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2014· Teleflex Medical

Recalled Item: 5/10 mm Weck Vista Universal Cannula Recalled by Teleflex Medical Due to...

The Issue: Complaints of leakage of insufflation gas through the device.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2014· Teleflex Medical

Recalled Item: Weck Vista Universal Laparoscopic Port Recalled by Teleflex Medical Due to...

The Issue: Complaints of leakage of insufflation gas through the device.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2014· Teleflex Medical

Recalled Item: 5/10 Weck¿ Vista" Universal Balloon Open Access Port - Standard Length...

The Issue: Complaints were received of leakage of insufflation gas through the device,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2014· Teleflex Medical

Recalled Item: 5/10/12 mm x 100mm Weck Vista Universal Cone Open Access Recalled by...

The Issue: Complaints of leakage of insufflation gas through the device.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2014· Teleflex Medical

Recalled Item: 5/10/12 mm Weck¿ Vista" Universal Cannula Recalled by Teleflex Medical Due...

The Issue: Complaints were received of leakage of insufflation gas through the device,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2014· Teleflex Medical

Recalled Item: 10mm Weck Vista Cannula-only Recalled by Teleflex Medical Due to Complaints...

The Issue: Complaints of leakage of insufflation gas through the device.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2014· Teleflex Medical

Recalled Item: 5/10 mm Weck Vista Optical Bladeless Laparoscopic Access Port Recalled by...

The Issue: Complaints of leakage of insufflation gas through the device.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2014· Teleflex Medical

Recalled Item: Sutures Recalled by Teleflex Medical Due to The products are being recalled...

The Issue: The products are being recalled because they did not meet minimum needle...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2014· Teleflex Medical

Recalled Item: Nonabsorbable Surgical Suture Recalled by Teleflex Medical Due to Product...

The Issue: Product does not meet minimum needle attachment strength requirements; thus,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2014· Teleflex Medical

Recalled Item: Teleflex Medical Recalled by Teleflex Medical Due to Product does not meet...

The Issue: Product does not meet minimum needle attachment strength requirements; thus,...

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

Class II — Potential Health HazardOngoing
DrugMarch 11, 2014· Paddock Laboratories, LLC

Recalled Item: Perrigo Recalled by Paddock Laboratories, LLC Due to Presence of Particulate...

The Issue: Presence of Particulate Matter Perrigo is recalling seven lots of...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMarch 10, 2014· AbbVie Inc

Recalled Item: Lupron Depot (Leuprolide Acetate for Depot Suspension) Single Dose...

The Issue: Defective Delivery System: Some Lupron Depot Kits may contain a syringe with...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMarch 10, 2014· AbbVie Inc

Recalled Item: Lupron Depot (leuprolide acetate for depot suspension) Single Dose...

The Issue: Defective Delivery System: Some Lupron Depot Kits may contain a syringe with...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMarch 10, 2014· AbbVie Inc

Recalled Item: Lupron Depot (Leuprolide Acetate for Depot Suspension) Single Dose...

The Issue: Defective Delivery System: Some Lupron Depot Kits may containin a syringe...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMarch 10, 2014· AbbVie Inc

Recalled Item: Lupron Depot (Leuprolide Acetate for Depot Suspension) Single Dose...

The Issue: Defective Delivery System: Some Lupron Depot Kits may contain a syringe with...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMarch 10, 2014· AbbVie Inc

Recalled Item: LUPRON DEPOT-PED (Leuprolide Acetate for Depot Suspension) Single Dose...

The Issue: Defective Delivery System: Some Lupron Depot Kits may contain a syringe with...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 10, 2014· Del Mar Reynolds Medical, Ltd.

Recalled Item: SpaceLabs Arkon Anesthesia Delivery System with Version 2.0 Software...

The Issue: The System may go into a controlled failed state if a series of parameters...

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

Class I — Serious Health HazardOngoing