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. 1,914 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
1,914 in last 12 months

Showing 3100131020 of 55,896 recalls

DrugOctober 10, 2017· Banner Pharmacy Services, LLC

Recalled Item: fentanyl citrate (PF) 1100 mcg (20 mcg/mL) 55 mL syringes Recalled by Banner...

The Issue: Lack of Assurance of Sterility.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 10, 2017· Banner Pharmacy Services, LLC

Recalled Item: Succinylcholine 200 mg/10 mL Syringe Recalled by Banner Pharmacy Services,...

The Issue: Lack of Assurance of Sterility.

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 10, 2017· La Terra Fina, Inc.

Recalled Item: La Terra Fina Spinach Artichoke & Parmesan Dip & Spread Recalled by La Terra...

The Issue: Undeclared allergen; egg.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceOctober 10, 2017· Crimson Trace Corporation

Recalled Item: Crimson Trace Corporation laser sights. The Finished Products are laser...

The Issue: A previously "in specification" Finished Product with a Model 25-0657 diode...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2017· Implant Direct Sybron Manufacturing, LLC

Recalled Item: ImplantDirect Legacy(TM) 3 Implant Recalled by Implant Direct Sybron...

The Issue: One reported complaint and discovered that the outer vial was out of round...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2017· Karl Storz Endoscopy

Recalled Item: STORZ High Flow Insufflation Tubing (with filter) Recalled by Karl Storz...

The Issue: The label outside the cardboard box is labeled correctly but the pouches...

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

Class II — Potential Health HazardOngoing
FoodOctober 9, 2017· General Mills, Inc

Recalled Item: Cascadian Farm Organic Cinnamon Raisin Granola Recalled by General Mills,...

The Issue: General Mills is recalling 2 production runs of Cascadian Farm Organic...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceOctober 9, 2017· Exactech, Inc.

Recalled Item: Alteon HA Femoral Stem Recalled by Exactech, Inc. Due to Wrong device...

The Issue: Wrong device description of the label identifying the implant

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

Class II — Potential Health HazardOngoing
DrugOctober 6, 2017· NEW RELIANCE TRADING, INC.

Recalled Item: No.1 Faiza Beauty Cream Manufactured by: Poonia Brothers (Pak) Recalled by...

The Issue: Marketed Without an Approved NDA/ANDA

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 6, 2017· AVKARE Inc.

Recalled Item: Duloxetine Delayed-release Capsules USP Recalled by AVKARE Inc. Due to...

The Issue: Failed Impurities/Degradation Specifications: slightly elevated levels of...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 6, 2017· Kiriko, LLC.

Recalled Item: A1 Slim Recalled by Kiriko, LLC. Due to Undeclared Sibutramine

The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis found this product to...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 6, 2017· Cooperstown Cheese Company, LLC

Recalled Item: Toma Celena Recalled by Cooperstown Cheese Company, LLC Due to Potential...

The Issue: Cheese may be contaminated with Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 6, 2017· Cooperstown Cheese Company, LLC

Recalled Item: Roasted Garlic and Black Peppercorns. All package sizes are subject Recalled...

The Issue: Cheese may be contaminated with Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 6, 2017· Cooperstown Cheese Company, LLC

Recalled Item: Roasted Garlic Cheddar Recalled by Cooperstown Cheese Company, LLC Due to...

The Issue: Cheese may be contaminated with Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 6, 2017· Whole Foods Market Brand 365, Llc

Recalled Item: 365 Organic Raisin Bran Flakes 15 oz. packaged in plastic bag Recalled by...

The Issue: Undeclared (peanut) allergen: 365 Organic Peanut Butter and Cocoa Balls were...

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 6, 2017· Bel Brands USA

Recalled Item: Merkts Port Wine Cheese Spread Recalled by Bel Brands USA Due to Bel Brands...

The Issue: Bel Brands USA is recalling Merkts Port Wine Cheese Spread after being...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 6, 2017· CooperSurgical, Inc.

Recalled Item: Cooper Surgical 2 MHZ Waterproof OB Probe Product The CooperSurgical...

The Issue: The 2MHZ prove was...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2017· Allen Medical Systems

Recalled Item: Radiolucent Surgery Spine Frame (F70801). Surgical platform used to position...

The Issue: The base of the frame has the potential to crack when the patient is...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2017· Allen Medical Systems

Recalled Item: Allen Medical Bow Frame Model A-70800. Surgical platform used to Recalled by...

The Issue: The base of the frame has the potential to crack when the patient is...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2017· Halyard Health, Inc

Recalled Item: Halyard Closed Suction System for Adults Recalled by Halyard Health, Inc Due...

The Issue: Received recall notification from Smiths Medical that lots of 15ml Saline...

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

Class II — Potential Health HazardOngoing