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. 2,648 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
2,648 in last 12 months

Showing 3064130660 of 55,896 recalls

DrugNovember 16, 2017· KRS Global Biotechnology, Inc

Recalled Item: T-105 (Prostaglandin E1 Recalled by KRS Global Biotechnology, Inc Due to...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD)...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 16, 2017· KRS Global Biotechnology, Inc

Recalled Item: Chloramphenicol 500 mg Amphotericin 50 mg Otic Powder packaged in jars...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD)...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 16, 2017· KRS Global Biotechnology, Inc

Recalled Item: 7-Ketodehydroepiandrosterone (7-Keto DHEA) 100 mg Capsule Recalled by KRS...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD)...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 16, 2017· KRS Global Biotechnology, Inc

Recalled Item: Anastrozole SR 1 mg Capsules Recalled by KRS Global Biotechnology, Inc Due...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD)...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 16, 2017· KRS Global Biotechnology, Inc

Recalled Item: Hydroxocobalamin 1 mg/mL 30 mL Vial For IM Use Recalled by KRS Global...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD)...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 16, 2017· KRS Global Biotechnology, Inc

Recalled Item: Sermorelin Acetate 3 mg/ GHRP6 3 mg Recalled by KRS Global Biotechnology,...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD)...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 16, 2017· Sichuan Youjia Foodstuffs Co., Ltd

Recalled Item: BAMBOO SHOOTS SAUCE (Marinated Bamboo) packaged in a glass jar Recalled by...

The Issue: Low water activity controlled product found with water activity above .85

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 16, 2017· Maple Hill Creamery, LLC

Recalled Item: Maple Hill Creamery Recalled by Maple Hill Creamery, LLC Due to Visible...

The Issue: Visible spoilage of product before the end of shelf life.

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

Class III — Low RiskOngoing
Refund
Medical DeviceNovember 15, 2017· Cordis Corporation

Recalled Item: Cordis S.M.A.R.T. Flex Biliary Stent System Product Usage: Is indicated...

The Issue: Potential for cracked luer hubs

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2017· Implant Direct Sybron Manufacturing, LLC

Recalled Item: Spectra System/Legacy Guided Surgery Handle Kit (Part Number: G-HK) Spectra...

The Issue: The Spectra System/Legacy Guided Surgery Handle Kit had guided handle...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2017· Arrow International Inc

Recalled Item: Pressure Injectable Multi- Lumen CVC Kit Recalled by Arrow International Inc...

The Issue: Products do not contain the Central Venous Catheter Placement Procedures...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2017· Arrow International Inc

Recalled Item: ARROWg+ard Blue PLUS Pressure Injectable Multi-Lumen CVC Kit. Intended to...

The Issue: Products do not contain the Central Venous Catheter Placement Procedures...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2017· Arrow International Inc

Recalled Item: Pressure Injectable Multi- Lumen Central Venous Catheterization Kit with...

The Issue: Products do not contain the Central Venous Catheter Placement Procedures...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2017· Arrow International Inc

Recalled Item: Percutaneous Sheath Introducer Kit with Integral Hemostasis Valve/Side Port...

The Issue: Products do not contain the Central Venous Catheter Placement Procedures...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2017· Arrow International Inc

Recalled Item: Percutaneous Sheath Introducer Kit with ARROWg+ard Blue Sheath Recalled by...

The Issue: Products do not contain the Central Venous Catheter Placement Procedures...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2017· Arrow International Inc

Recalled Item: Pressure Injectable Multi- Lumen Central Venous Catheterization Kit with...

The Issue: Products do not contain the Central Venous Catheter Placement Procedures...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2017· Arrow International Inc

Recalled Item: Pressure Injectable Two- Lumen Central Venous Catheterization Kit with Blue...

The Issue: Products do not contain the Central Venous Catheter Placement Procedures...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2017· Arrow International Inc

Recalled Item: Pressure Injectable Multi- Lumen Central Venous Catheterization Kit with...

The Issue: Products do not contain the Central Venous Catheter Placement Procedures...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2017· Arrow International Inc

Recalled Item: Pressure Injectable Multi- Lumen Central Venous Catheterization Kit with...

The Issue: Products do not contain the Central Venous Catheter Placement Procedures...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2017· Alere San Diego, Inc.

Recalled Item: Triage Drugs of Abuse Plus TCA 25 Test Kit Recalled by Alere San Diego, Inc....

The Issue: The recalled lots have demonstrated unexpected false positive THC results.

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

Class II — Potential Health HazardOngoing