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. 2,748 recalls have been distributed to New York in the last 12 months.
Showing 17521–17540 of 30,153 recalls
Recalled Item: Artis one fluoroscopic x-ray system and patient table Artis one Recalled by...
The Issue: Certain patient table systems may have a missing or incorrectly installed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE HEALTHCARE CARESCAPE Central Station (CSCS) software version 2.0.2 The...
The Issue: CARESCAPE Central Station (CSCS) software version 2.0.2 units may experience...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ellex I.Science iTRACK 250A Recalled by Ellex iScience, Inc. Due to...
The Issue: Sterility failure found in one of the units in the lot.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PDS Plus Antibacterial (Polydioxanone) Suture Size 0 PDS Plus Violet...
The Issue: Three (3) lots were distributed with the incorrect expiry date on the label....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PDS Plus Antibacterial (Polydioxanone) Suture Size 0 PDS Plus Violet...
The Issue: Three (3) lots were distributed with the incorrect expiry date on the label....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PDS Plus Antibacterial (Polydioxanone) Suture Size 1 PDS PLUS Violet...
The Issue: Three (3) lots were distributed with the incorrect expiry date on the label....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RP RIVERPOINT MEDICAL 18G Brachy Grid B&K(TM) style Recalled by Riverpoint...
The Issue: Product is labeled with "CE", but is not yet approved in the European Union.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemodynamic monitoring system (HMS) Recalled by ICU Medical, Inc. Due to...
The Issue: When continuous cardiac output monitoring with a pulmonary artery catheter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diamedix Is-EBV-EA-D IgG Enzyme Immunoassay Test Kit for In Vitro Recalled...
The Issue: Contains a gel-like contaminant that may affect product performance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diamedix Is-Mumps IgG Enzyme Immunoassay Test Kit for In Vitro Recalled by...
The Issue: Contains a gel-like contaminant that may affect product performance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioMerieux mini VIDAS System in combination with Quality Control VIDAS*...
The Issue: Increase of events affecting performance regarding pump clogging and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioMerieux VIDAS System in combination with Quality Control VIDAS* (QCV*)...
The Issue: Increase of events affecting performance regarding pump clogging and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diagnostic Ultrasound System Recalled by Toshiba American Medical Systems...
The Issue: The power supply unit may be damaged and may fail to start up when the power...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper systems with Certeray X-ray Generator located in regions...
The Issue: There is an increase in the failure rate of certain Anode Drive Units (ADU5)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trabecular Metal¿ Primary Hip Prosthesis Recalled by Zimmer Biomet, Inc. Due...
The Issue: Two lots of hip implants are mislabeled.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance Big Bore Radiology CT with 4.2.0 software version. Model Recalled...
The Issue: Software issues including: Software errors that may result in Extended Field...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance Big Bore Oncology CTwith 4.2.0 software version. Model #'...
The Issue: Software issues including: Software errors that may result in Extended Field...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percuvance(R) Percutaneous Shaft 36cm Recalled by Teleflex Medical Due to...
The Issue: There is potential for a piece of the distal tip on the Percuvance shaft to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percuvance(R) Percutaneous Shaft 29cm Recalled by Teleflex Medical Due to...
The Issue: There is potential for a piece of the distal tip on the Percuvance shaft to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE ¿ 2000/IMMULITE ¿ 2000 XPi Gastrin Recalled by Siemens Healthcare...
The Issue: Concentrations for the level of biotin that does not interfere is not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.