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. 1,098 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
1,098 in last 12 months

Showing 19921–19940 of 55,896 recalls

DrugJuly 27, 2020· Broncolin, S.A. de C.V.

Recalled Item: HERBACIL Recalled by Broncolin, S.A. de C.V. Due to CGMP Deviations:...

The Issue: CGMP Deviations: products were recalled because they were manufactured in...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 27, 2020· Broncolin, S.A. de C.V.

Recalled Item: HERBACIL Recalled by Broncolin, S.A. de C.V. Due to Chemical Contamination:...

The Issue: Chemical Contamination: HERBACIL, Antiseptic Hand Sanitizer, 70% Alcohol,...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJuly 27, 2020· C.A. Greiner & Sohne Gesellschaftmbh

Recalled Item: Plastic Cannula HOLDEX Item # 450216 - Product Usage: - Recalled by C.A....

The Issue: Sample leaking from the sleeve covering the needle inside the cannula

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2020· Office Depot Inc

Recalled Item: JINYINSHAN Recalled by Office Depot Inc Due to Test results revealed that...

The Issue: Test results revealed that the KN95 masks failed to filter greater than 95%...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2020· Karl Storz Endoscopy

Recalled Item: Flexible Intubation Video Endoscope Recalled by Karl Storz Endoscopy Due to...

The Issue: Updated sterilization instructions are being provided to ensure 1) a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2020· Medical Components, Inc dba MedComp

Recalled Item: Medcomp 15.SF X 24CM Titan HD CATHETER (CUFF 19CM FROM TIP) Recalled by...

The Issue: Kits were packaged with the incorrect size valve peelable introducer. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2020· Datascope Corporation

Recalled Item: Datascope Intra-Aortic Ballon Catheters (IABs)-Sensation 7Fr 40cc IAB Kit...

The Issue: Potential Endotoxin Contamination

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2020· Datascope Corporation

Recalled Item: Datascope Intra-Aortic Ballon Catheters (IABs)-TRANS-RAY PLUS 7.5Fr 40cc IAB...

The Issue: Potential Endotoxin Contamination

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2020· Karl Storz Endoscopy

Recalled Item: Flexible DCI Intubation Fiberscope Recalled by Karl Storz Endoscopy Due to...

The Issue: Updated sterilization instructions are being provided to ensure 1) a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2020· Datascope Corporation

Recalled Item: Datascope Intra-Aortic Ballon Catheters (IABs)-Sensation 7Fr 34cc IAB Kit...

The Issue: Potential Endotoxin Contamination

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2020· Datascope Corporation

Recalled Item: Datascope Intra-Aortic Ballon Catheters (IABs)-Sensation Plus 7.5 Fr 40cc...

The Issue: Potential Endotoxin Contamination

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2020· Datascope Corporation

Recalled Item: Datascope Intra-Aortic Ballon Catheters (IABs)-YAMATO PLUS-R 7.5Fr 30cc IAB...

The Issue: Potential Endotoxin Contamination

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2020· Datascope Corporation

Recalled Item: Datascope Intra-Aortic Ballon Catheters (IABs)-Linear 7.5Fr 40cc IAB Kit...

The Issue: Potential Endotoxin Contamination

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2020· Datascope Corporation

Recalled Item: Datascope Intra-Aortic Balloon Catheters (IABs)-MEGA 7.5Fr 40cc IAB Kit P/N:...

The Issue: Potential Endotoxin Contamination

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2020· Datascope Corporation

Recalled Item: Datascope Intra-Aortic Ballon Catheters (IABs)-Trans-Ray 7Fr 34cc IAB...

The Issue: Potential Endotoxin Contamination

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2020· Karl Storz Endoscopy

Recalled Item: Flexible Intubation Video Endoscope Recalled by Karl Storz Endoscopy Due to...

The Issue: Updated sterilization instructions are being provided to ensure 1) a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2020· Datascope Corporation

Recalled Item: Datascope Intra-Aortic Ballon Catheters (IABs)-YAMATO PLUS-R 7.5Fr 40cc IAB...

The Issue: Potential Endotoxin Contamination

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2020· Datascope Corporation

Recalled Item: Datascope Intra-Aortic Ballon Catheters (IABs)-MEGA 7.5Fr 30cc IAB Recalled...

The Issue: Potential Endotoxin Contamination

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2020· Karl Storz Endoscopy

Recalled Item: Flexible Intubation Video Endoscope Recalled by Karl Storz Endoscopy Due to...

The Issue: Updated sterilization instructions are being provided to ensure 1) a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2020· Datascope Corporation

Recalled Item: Datascope Intra-Aortic Ballon Catheters (IABs)-YAMATO PLUS-R 7.5Fr 35cc IAB...

The Issue: Potential Endotoxin Contamination

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

Class II — Potential Health HazardOngoing