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 5364153660 of 55,896 recalls

FoodOctober 17, 2012· Bucks Ice Cream

Recalled Item: Iskream brand Peanut Butter and Jelly No Sugar Added Recalled by Bucks Ice...

The Issue: Ice Cream manufactured with Sunland recalled peanut butter has the potential...

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 17, 2012· Dole Fresh Vegetables Inc

Recalled Item: Dole American Blend Recalled by Dole Fresh Vegetables Inc Due to Potential...

The Issue: Tennessee Department of Agriculture collected a random sample of Dole...

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 17, 2012· Energy Club Inc

Recalled Item: Peanuts in Shell Recalled by Energy Club Inc Due to Potential Salmonella...

The Issue: Trifecta Foods, LLC in Pacoima, CA is voluntarily recalling products...

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 17, 2012· Natural Selection Foods LLC dba Earthbound Farm

Recalled Item: Earthbound Farms Organic Baby Spinach Grab & Go Salad Recalled by Natural...

The Issue: Peanuts packaged with EarthBound Baby Spinach Grab & Go Salad were provided...

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 17, 2012· Energy Club Inc

Recalled Item: Peanuts in Shell Recalled by Energy Club Inc Due to Potential Salmonella...

The Issue: Trifecta Foods, LLC in Pacoima, CA is voluntarily recalling products...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceOctober 17, 2012· Biomerieux Inc

Recalled Item: 0.9% Sodium Chloride Injections Recalled by Biomerieux Inc Due to The firm...

The Issue: The firm inventoried and distributed 0.9% Sodium Chloride Saline bags as...

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

Class II — Potential Health HazardOngoing
FoodOctober 16, 2012· Mondelez Global Llc

Recalled Item: Green & Black's Organic Peanut & Sea Salt Milk Chocolate Recalled by...

The Issue: Mondelez Global LLC (Mondelez Global) is voluntarily recalling the U.S....

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 16, 2012· PureFit Inc

Recalled Item: PureFit Peanut Butter Bars Recalled by PureFit Inc Due to Potential...

The Issue: PureFit is recalling PureFit Peanut Butter Crunch Bars because of possible...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceOctober 16, 2012· Biomerieux Inc

Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling

The Issue: The product may mislabel patient information on culture specimen bottles due...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2012· Biomerieux Inc

Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling

The Issue: The product may mislabel patient information on culture specimen bottles due...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2012· Biomerieux Inc

Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling

The Issue: The product may mislabel patient information on culture specimen bottles due...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2012· Biomerieux Inc

Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling

The Issue: The product may mislabel patient information on culture specimen bottles due...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2012· Biomerieux Inc

Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling

The Issue: The product may mislabel patient information on culture specimen bottles due...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2012· Biomerieux Inc

Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling

The Issue: The product may mislabel patient information on culture specimen bottles due...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2012· Biomerieux Inc

Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling

The Issue: The product may mislabel patient information on culture specimen bottles due...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2012· Biomerieux Inc

Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling

The Issue: The product may mislabel patient information on culture specimen bottles due...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2012· Biomerieux Inc

Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling

The Issue: The product may mislabel patient information on culture specimen bottles due...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2012· Vital Signs Devices, a GE Healthcare Company

Recalled Item: Corometrics Qwik Connect Plus Spiral Electrode- Model #7000AA0 A fetal...

The Issue: Thirty fetal scalp electrodes were found to have an incomplete package seal...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2012· Biomerieux Inc

Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling

The Issue: The product may mislabel patient information on culture specimen bottles due...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2012· Biomerieux Inc

Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling

The Issue: The product may mislabel patient information on culture specimen bottles due...

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

Class II — Potential Health HazardOngoing