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. 2,659 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
2,659 in last 12 months

Showing 2534125360 of 55,896 recalls

FoodApril 15, 2019· Juices International, Inc.

Recalled Item: All Juice Drinks and Beverages in 12 ounce glass bottles Recalled by Juices...

The Issue: FDA Issued Shutdown Letter ordering the recall of all produced juices in...

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 14, 2019· Schreiber Foods Inc

Recalled Item: Great Value Recalled by Schreiber Foods Inc Due to Foreign Object Contamination

The Issue: Product is being recalled due to the presence of foreign material (hard...

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 14, 2019· Schreiber Foods Inc

Recalled Item: Shredded and blocks of Colby & Monterey Jack cheese - Recalled by Schreiber...

The Issue: Product is being recalled due to the presence of foreign material (hard...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 12, 2019· OMNIlife science Inc.

Recalled Item: OMNIBotics iBlock Cutting Guide Recalled by OMNIlife science Inc. Due to The...

The Issue: The OMNIBotics iBlock Cutting Guide does not lock onto the iBlock Saw Guide...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2019· Geistlich Pharma North America, Inc.

Recalled Item: Geistlich Bio-Oss Pen Recalled by Geistlich Pharma North America, Inc. Due...

The Issue: When unscrewing the green cap from the pen, a visible piece of green plastic...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2019· Tecan US, Inc.

Recalled Item: Freedom EVO 200 - Product Usage: It is intended for routine laboratory tasks...

The Issue: Gas springs not always replaced within the interval specified.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2019· Geistlich Pharma North America, Inc.

Recalled Item: Geistlich Bio-Oss Pen Recalled by Geistlich Pharma North America, Inc. Due...

The Issue: When unscrewing the green cap from the pen, a visible piece of green plastic...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2019· TIDI PRODUCTS

Recalled Item: Posey Connected Twice-As-Tough Cuffs Recalled by TIDI PRODUCTS Due to Not...

The Issue: Not meeting design specifications.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2019· Bard Peripheral Vascular Inc

Recalled Item: BD WAVELINQ 4F EndoAVF System Recalled by Bard Peripheral Vascular Inc Due...

The Issue: The firm has become aware of a potential problem with their venous and...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2019· Geistlich Pharma North America, Inc.

Recalled Item: Geistlich Bio-Oss Pen Recalled by Geistlich Pharma North America, Inc. Due...

The Issue: When unscrewing the green cap from the pen, a visible piece of green plastic...

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

Class II — Potential Health HazardOngoing
DrugApril 12, 2019· Teva Pharmaceuticals USA

Recalled Item: Amoxicillin for Oral Suspension USP Recalled by Teva Pharmaceuticals USA Due...

The Issue: Subpotent Product: assay results for Amoxicillin were below the...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 11, 2019· Ethicon Endo-Surgery Inc

Recalled Item: Straight Intraluminal Staplers Recalled by Ethicon Endo-Surgery Inc Due to...

The Issue: The staplers may have an insufficient firing stroke to break the washer and...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 11, 2019· Intuitive Surgical Inc

Recalled Item: da Vinci X Surgical System Recalled by Intuitive Surgical Inc Due to Failure...

The Issue: Failure of Universal Surgical Manipulators due to a high friction points,...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2019· Intuitive Surgical Inc

Recalled Item: da Vinci Xi Surgical System Recalled by Intuitive Surgical Inc Due to...

The Issue: Failure of Universal Surgical Manipulators due to a high friction points,...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2019· Ethicon Endo-Surgery Inc

Recalled Item: Curved Intraluminal Staplers Recalled by Ethicon Endo-Surgery Inc Due to The...

The Issue: The staplers may have an insufficient firing stroke to break the washer and...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 11, 2019· Ethicon Endo-Surgery Inc

Recalled Item: Endoscopic Curved Intraluminal Stapler Recalled by Ethicon Endo-Surgery Inc...

The Issue: The staplers may have an insufficient firing stroke to break the washer and...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 11, 2019· Ethicon Endo-Surgery Inc

Recalled Item: Curved Intraluminal Staplers Recalled by Ethicon Endo-Surgery Inc Due to The...

The Issue: The staplers may have an insufficient firing stroke to break the washer and...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 11, 2019· Ethicon Endo-Surgery Inc

Recalled Item: Curved Intraluminal Staplers Recalled by Ethicon Endo-Surgery Inc Due to The...

The Issue: The staplers may have an insufficient firing stroke to break the washer and...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 11, 2019· Ethicon Endo-Surgery Inc

Recalled Item: Straight Intraluminal Staplers Recalled by Ethicon Endo-Surgery Inc Due to...

The Issue: The staplers may have an insufficient firing stroke to break the washer and...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 11, 2019· Ethicon Endo-Surgery Inc

Recalled Item: Endoscopic Curved Intraluminal Stapler Recalled by Ethicon Endo-Surgery Inc...

The Issue: The staplers may have an insufficient firing stroke to break the washer and...

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

Class I — Serious Health HazardOngoing