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. 1,141 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
1,141 in last 12 months

Showing 14521–14540 of 30,153 recalls

Medical DeviceApril 23, 2019· Arrow International Inc

Recalled Item: Arrow PICC Kit Product Code: ASK 45541 RWJ4 Recalled by Arrow International...

The Issue: Lidstock states the incorrect expiration date for the product

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2019· Arrow International Inc

Recalled Item: Arrow¿ JACC with Chlorag+ard Technology Product Code:JR 42563 HPHNM Recalled...

The Issue: Lidstock states the incorrect expiration date for the product

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2019· Arrow International Inc

Recalled Item: Arrow¿ JACC with Chlorag+ard¿ Technology Jugular Axillosubclavian Central...

The Issue: Lidstock states the incorrect expiration date for the product

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2019· Arrow International Inc

Recalled Item: Arrow¿ JACC with Chlorag+ard Technology Product Code: JR 42063 HPHNM...

The Issue: Lidstock states the incorrect expiration date for the product

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2019· Arrow International Inc

Recalled Item: Arrow PICC with Chlorag+ard Technology Product Code: CDA 45041 HPK1A...

The Issue: Lidstock states the incorrect expiration date for the product

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2019· Arrow International Inc

Recalled Item: Arrowg+ard Blue Advance JACC Product Code: CDC 42063 JX1A Recalled by Arrow...

The Issue: Lidstock states the incorrect expiration date for the product

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2019· CooperSurgical, Inc.

Recalled Item: LEEP Precision Integrated System 120V Recalled by CooperSurgical, Inc. Due...

The Issue: 2.5A slow blow fuses may have been installed in the LEEP RPECISION Generator...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2019· Arrow International Inc

Recalled Item: Arrow JACC with Chlorag+ard Technology Jugular Axillo subclavian Central...

The Issue: Lidstock states the incorrect expiration date for the product

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2019· Arrow International Inc

Recalled Item: Arrowg+ard Blue Advance JACC Product Code: JRT 43541 HPHNM Recalled by Arrow...

The Issue: Lidstock states the incorrect expiration date for the product

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2019· Arrow International Inc

Recalled Item: Arrow¿ PICC with Chlorag+ard¿ Technology Product Code: PR 45541 HPHNL...

The Issue: Lidstock states the incorrect expiration date for the product

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2019· Stryker Corporation

Recalled Item: Stryker Connected OR Cart Recalled by Stryker Corporation Due to There is a...

The Issue: There is a potential problem with firm s Connected OR Cart, 120V resulting...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2019· Cook Inc.

Recalled Item: Cook Salle Intraoperative Pyeloplasty Stent Set PRODUCT/CATALOG NUMBER/GPN:...

The Issue: Kwart RetroInject Stent Set (Multi-Length) and Salle Intraoperative...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2019· Cook Inc.

Recalled Item: Cook Kwart Retro-Inject Ureteral Stent Set: PRODUCT/CATALOG NUMBER/GPN: 4.7...

The Issue: Kwart RetroInject Stent Set (Multi-Length) and Salle Intraoperative...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 19, 2019· Philips North America, LLC

Recalled Item: SureSigns VS4 NBP Recalled by Philips North America, LLC Due to System...

The Issue: System software inhibits the monitor and as a result does not measure,...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 19, 2019· AURIS HEALTH INC

Recalled Item: Monarch Recalled by AURIS HEALTH INC Due to Reports of aspirating biopsy...

The Issue: Reports of aspirating biopsy needle breakage

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 19, 2019· Isopure Corp

Recalled Item: Finish Thompson Centrifugal Pump Model #110192-3 (sold as spare part)...

The Issue: There is a potential for an uneven plastic encapsulation of the magnet ring...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 19, 2019· Isopure Corp

Recalled Item: Isopure Sodium Bicarbonate Mixing and Distribution System (IsoMix PRO) with...

The Issue: There is a potential for an uneven plastic encapsulation of the magnet ring...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 19, 2019· Isopure Corp

Recalled Item: Acidified Concentrate Distribution and Storage System (ACDS System) with a...

The Issue: There is a potential for an uneven plastic encapsulation of the magnet ring...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 19, 2019· Ethicon, Inc.

Recalled Item: ETHIBOND EXCEL¿ Polyester Suture-ETHIBOND Green 75cm USP1 Single Armed CT-1...

The Issue: Possibility that a suture raw material containing high endotoxin levels was...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 19, 2019· Ethicon, Inc.

Recalled Item: ETHIBOND EXCEL ETHIBOND Polvester Suture-Green 75cm USP1 Single Armed CTX...

The Issue: Possibility that a suture raw material containing high endotoxin levels was...

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

Class II — Potential Health HazardOngoing