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. 2,564 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
2,564 in last 12 months

Showing 5582155840 of 55,896 recalls

Medical DeviceMarch 6, 2009· Exactech, Inc.

Recalled Item: Altiva / Exactech Spine Recalled by Exactech, Inc. Due to Incorrect thread...

The Issue: Incorrect thread form on the screw.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2009· Invatec Llc

Recalled Item: lnvatec SpA brand Diver C.E. Recalled by Invatec Llc Due to Devices labeled...

The Issue: Devices labeled for an intended use was not included in the existing 510(k)...

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

Class II — Potential Health HazardOngoing
FoodFebruary 6, 2009· Giannios Candy Co Inc

Recalled Item: Milk Chocolate Catalog # 111 Recalled by Giannios Candy Co Inc Due to...

The Issue: This product is being recalled because it was manufactured using peanut...

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 3, 2009· Gorant Candies Inc A Division of Carlton Cards Retail Inc

Recalled Item: No Sugar Added Milk Chocolate Peanuts in 10 oz and 3 oz bags Recalled by...

The Issue: The product is being recalled because it was manufactured using peanuts that...

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 3, 2009· Gorant Candies Inc A Division of Carlton Cards Retail Inc

Recalled Item: Chocolate bridge mix in 10 oz Recalled by Gorant Candies Inc A Division of...

The Issue: The product is being recalled because it was manufactured using peanuts that...

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 3, 2009· Gorant Candies Inc A Division of Carlton Cards Retail Inc

Recalled Item: Milk Chocolate Peanuts in 10 oz Recalled by Gorant Candies Inc A Division of...

The Issue: The product is being recalled because it was manufactured using peanuts that...

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 3, 2009· Gorant Candies Inc A Division of Carlton Cards Retail Inc

Recalled Item: No Sugar Added Bridge Mix in 12 oz bags Recalled by Gorant Candies Inc A...

The Issue: The product is being recalled because it was manufactured using peanuts that...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJanuary 25, 2009· Zynex Medical, Inc.

Recalled Item: IF 8000 Recalled by Zynex Medical, Inc. Due to Zynex notified customers that...

The Issue: Zynex notified customers that a malfunction in the IF 8000 can result in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2009· NuVasive Inc

Recalled Item: 5.5mm x 55mm Cannulated Screw Shank Subsequent Codes: KWP Recalled by...

The Issue: The tulip portion of the screw assembly can disengage from the shank after...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2009· NuVasive Inc

Recalled Item: 4.5mm x 35mm Noncannulated Screw Shank Subsequent Codes: KWP Recalled by...

The Issue: The tulip portion of the screw assembly can disengage from the shank after...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2009· NuVasive Inc

Recalled Item: 6.5mm x 40mm Cannulated Screw Shank Subsequent Codes: KWP Recalled by...

The Issue: The tulip portion of the screw assembly can disengage from the shank after...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2009· NuVasive Inc

Recalled Item: 7.5mm x 30mm Cannulated Screw Shank Subsequent Codes: KWP Recalled by...

The Issue: The tulip portion of the screw assembly can disengage from the shank after...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2009· NuVasive Inc

Recalled Item: 7.5mm x 40mm Noncannulated Screw Shank Subsequent Codes: KWP Recalled by...

The Issue: The tulip portion of the screw assembly can disengage from the shank after...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2009· NuVasive Inc

Recalled Item: 5.5mm x 45mm Cannulated Screw Shank Subsequent Codes: KWP Recalled by...

The Issue: The tulip portion of the screw assembly can disengage from the shank after...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2009· NuVasive Inc

Recalled Item: 6.5mm x 50mm Cannulated Screw Shank Subsequent Codes: KWP Recalled by...

The Issue: The tulip portion of the screw assembly can disengage from the shank after...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2009· NuVasive Inc

Recalled Item: 6.5mm x 55mm Cannulated Screw Shank Subsequent Codes: KWP Recalled by...

The Issue: The tulip portion of the screw assembly can disengage from the shank after...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2009· NuVasive Inc

Recalled Item: 7.5mm x 50mm Noncannulated Screw Shank Subsequent Codes: KWP Recalled by...

The Issue: The tulip portion of the screw assembly can disengage from the shank after...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2009· NuVasive Inc

Recalled Item: Screw Tulip Recalled by NuVasive Inc Due to The tulip portion of the screw...

The Issue: The tulip portion of the screw assembly can disengage from the shank after...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2009· NuVasive Inc

Recalled Item: 7.5mm x 45mm Cannulated Screw Shank Subsequent Codes: KWP Recalled by...

The Issue: The tulip portion of the screw assembly can disengage from the shank after...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2009· NuVasive Inc

Recalled Item: 6.5mm x 40mm Noncannulated Screw Shank Subsequent Codes: KWP Recalled by...

The Issue: The tulip portion of the screw assembly can disengage from the shank after...

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

Class II — Potential Health HazardOngoing