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. 2,567 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
2,567 in last 12 months

Showing 4442144440 of 55,896 recalls

FoodJanuary 14, 2015· J P Veggies Inc. DBA VeggieLand

Recalled Item: Chili-Bean Fresh Veggiburger Recalled by J P Veggies Inc. DBA VeggieLand Due...

The Issue: Franklin Farms DBA VeggiLand is recalling their Chili-Bean Veggiburgers...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 14, 2015· INO Therapeutics (dba Ikaria)

Recalled Item: Ikaria Recalled by INO Therapeutics (dba Ikaria) Due to Potential delivery...

The Issue: Potential delivery failure alarm condition. INOmax DSIR with software...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 14, 2015· Teleflex Medical

Recalled Item: AQUAPAK 101 SW Recalled by Teleflex Medical Due to Foreign Object Contamination

The Issue: The packages may contain foreign material (black particles).

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 14, 2015· Teleflex Medical

Recalled Item: ADAPTOR Recalled by Teleflex Medical Due to Foreign Object Contamination

The Issue: The packages may contain foreign material (black particles).

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 14, 2015· Teleflex Medical

Recalled Item: AQUAPAK 640 SW Recalled by Teleflex Medical Due to Foreign Object Contamination

The Issue: The packages may contain foreign material (black particles).

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 14, 2015· Teleflex Medical

Recalled Item: AQUAPAK 340 SW Recalled by Teleflex Medical Due to Foreign Object Contamination

The Issue: The packages may contain foreign material (black particles).

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 14, 2015· Teleflex Medical

Recalled Item: AQUAPAK 340 SW Recalled by Teleflex Medical Due to Foreign Object Contamination

The Issue: The packages may contain foreign material (black particles).

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 14, 2015· Teleflex Medical

Recalled Item: AQUA 540 SW Recalled by Teleflex Medical Due to Foreign Object Contamination

The Issue: The packages may contain foreign material (black particles).

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 14, 2015· Teleflex Medical

Recalled Item: AQUAPAK SW/EAU STERILE Recalled by Teleflex Medical Due to Foreign Object...

The Issue: The packages may contain foreign material (black particles).

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 14, 2015· Teleflex Medical

Recalled Item: AQUAPAK 640 SW Recalled by Teleflex Medical Due to Foreign Object Contamination

The Issue: The packages may contain foreign material (black particles).

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 14, 2015· Teleflex Medical

Recalled Item: AQUAPAK 340 SW Recalled by Teleflex Medical Due to Foreign Object Contamination

The Issue: The packages may contain foreign material (black particles).

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 14, 2015· Teleflex Medical

Recalled Item: Hudson RCI¿ Humidifier Adaptor Recalled by Teleflex Medical Due to Foreign...

The Issue: The packages may contain foreign material (black particles).

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 14, 2015· Teleflex Medical

Recalled Item: AQUAPAK 640 SW Recalled by Teleflex Medical Due to Foreign Object Contamination

The Issue: The packages may contain foreign material (black particles).

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 14, 2015· Teleflex Medical

Recalled Item: AQUAPAK 340 SW Recalled by Teleflex Medical Due to Foreign Object Contamination

The Issue: The packages may contain foreign material (black particles).

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 14, 2015· Teleflex Medical

Recalled Item: AQUAPAK SW/EAU STERILE Recalled by Teleflex Medical Due to Foreign Object...

The Issue: The packages may contain foreign material (black particles).

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 14, 2015· Teleflex Medical

Recalled Item: AQUAPAK 640 SW Recalled by Teleflex Medical Due to Foreign Object Contamination

The Issue: The packages may contain foreign material (black particles).

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 14, 2015· Teleflex Medical

Recalled Item: AQUAPAK 340 SW Recalled by Teleflex Medical Due to Foreign Object Contamination

The Issue: The packages may contain foreign material (black particles).

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

Class II — Potential Health HazardOngoing
FoodJanuary 13, 2015· Gilster-Mary Lee Corp.

Recalled Item: Honey & Oat Mixers ready-to-eat dry cereal sold under the Recalled by...

The Issue: Undeclared almonds

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJanuary 13, 2015· Teleflex Medical

Recalled Item: LMA (Laryngeal Mask Airway) Supreme (New Cuff) Size 5 Recalled by Teleflex...

The Issue: The labelling of units from the affected lot indicates that it contains a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 13, 2015· Medtronic Sofamor Danek USA Inc

Recalled Item: KYPHON EXPRESS Recalled by Medtronic Sofamor Danek USA Inc Due to The...

The Issue: The product, labeled as containing, one bevel-tipped instrument and one...

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

Class II — Potential Health HazardOngoing