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. 1,935 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
1,935 in last 12 months

Showing 2880128820 of 55,896 recalls

DrugJune 12, 2018· Avella of Deer Valley, Inc. Store 38

Recalled Item: fentaNYL (10 mcg per mL) in 0.95 Sodium Chloride Recalled by Avella of Deer...

The Issue: Lack of Assurance of Sterility: Potential leakage of bags.

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 12, 2018· Avella of Deer Valley, Inc. Store 38

Recalled Item: 0.2% ROPivacaine Recalled by Avella of Deer Valley, Inc. Store 38 Due to...

The Issue: Lack of Assurance of Sterility: Potential leakage of bags.

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 12, 2018· Avella of Deer Valley, Inc. Store 38

Recalled Item: MORphine 1 mg/mL (Morphine Sulfate Recalled by Avella of Deer Valley, Inc....

The Issue: Lack of Assurance of Sterility: Potential leakage of bags.

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 12, 2018· Avella of Deer Valley, Inc. Store 38

Recalled Item: NORepiNEPHrine Bitartrate Recalled by Avella of Deer Valley, Inc. Store 38...

The Issue: Lack of Assurance of Sterility: Potential leakage of bags.

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 12, 2018· Avella of Deer Valley, Inc. Store 38

Recalled Item: HEPARIN 12 Recalled by Avella of Deer Valley, Inc. Store 38 Due to Lack of...

The Issue: Lack of Assurance of Sterility: Potential leakage of bags.

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 12, 2018· Dr. Reddy's Laboratories, Inc.

Recalled Item: Atorvastatin Calcium Tablets Recalled by Dr. Reddy's Laboratories, Inc. Due...

The Issue: Failed Impurities/Degradation Specifications

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

Class III — Low RiskOngoing
Refund
DrugJune 12, 2018· Dr. Reddy's Laboratories, Inc.

Recalled Item: Atorvastatin Calcium Tablets Recalled by Dr. Reddy's Laboratories, Inc. Due...

The Issue: Failed Impurities/Degradation Specifications

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

Class III — Low RiskOngoing
Refund
DrugJune 12, 2018· Dr. Reddy's Laboratories, Inc.

Recalled Item: Atorvastatin Calcium Tablets Recalled by Dr. Reddy's Laboratories, Inc. Due...

The Issue: Failed Impurities/Degradation Specifications

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

Class III — Low RiskOngoing
Refund
DrugJune 12, 2018· Avella of Deer Valley, Inc. Store 38

Recalled Item: ePHEDrine Sulfate Recalled by Avella of Deer Valley, Inc. Store 38 Due to...

The Issue: Lack of Assurance of Sterility: Potential leakage of bags.

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 12, 2018· Avella of Deer Valley, Inc. Store 38

Recalled Item: ceFAZolin 2 gm in NS 100mL. ceFAZolin Sodium (USP) 2gm Recalled by Avella of...

The Issue: Lack of Assurance of Sterility: Potential leakage of bags.

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 12, 2018· Avella of Deer Valley, Inc. Store 38

Recalled Item: HEPARIN 25 Recalled by Avella of Deer Valley, Inc. Store 38 Due to Lack of...

The Issue: Lack of Assurance of Sterility: Potential leakage of bags.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 12, 2018· Teleflex Medical Europe Ltd

Recalled Item: Teleflex MEDICAL Pilling(R) UNIVERSAL SHEARS 7 1/2" Recalled by Teleflex...

The Issue: The incorrect plastic was used to manufacture the handles of these shears,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2018· Inspire Medical Systems Inc.

Recalled Item: Inspire II Model 3024 Implantable Pulse Generator (IPG) for Obstructive...

The Issue: Incorrect use-by date on the device registration/patient file labels.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2018· Philips Respironics, Inc.

Recalled Item: Trilogy 100 Recalled by Philips Respironics, Inc. Due to In 2018, Philips...

The Issue: In 2018, Philips Respironics added foam replacement to the preventive...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 11, 2018· Withings Sas

Recalled Item: Nokia BPM+ Wireless Blood Pressure Monitor Product System Recalled by...

The Issue: Device could not meet the requirements for systolic pressure

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2018· Cardinal Health 200, LLC

Recalled Item: Hydroline Trumpet Valve Recalled by Cardinal Health 200, LLC Due to The...

The Issue: The suction valve may not close properly which could cause continuous suction.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2018· Cardinal Health 200, LLC

Recalled Item: Hydroline Trumpet Valve Recalled by Cardinal Health 200, LLC Due to The...

The Issue: The suction valve may not close properly which could cause continuous suction.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2018· Cardinal Health 200, LLC

Recalled Item: Hydroline Trumpet Valve Recalled by Cardinal Health 200, LLC Due to The...

The Issue: The suction valve may not close properly which could cause continuous suction.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2018· Philips Healthcare

Recalled Item: Centron Product Usage: Vascular Recalled by Philips Healthcare Due to The...

The Issue: The first time an operator selects a new procedure type during a single...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2018· Philips Healthcare

Recalled Item: Allura Xper Product Usage: Vascular Recalled by Philips Healthcare Due to...

The Issue: The first time an operator selects a new procedure type during a single...

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

Class II — Potential Health HazardOngoing