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 17641–17660 of 30,153 recalls
Recalled Item: Percutaneous Access Set Recalled by Boston Scientific Corporation Due to...
The Issue: Certain Malecot Nephrostomy Catheters are breaking at the mid-shaft bond...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Malecot Nephrostomy Catheter Set Recalled by Boston Scientific Corporation...
The Issue: Certain Malecot Nephrostomy Catheters are breaking at the mid-shaft bond...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Re-Entry" Malecot Nephrostomy Catheter Set Recalled by Boston Scientific...
The Issue: Certain Malecot Nephrostomy Catheters are breaking at the mid-shaft bond...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Re-Entry" Malecot Nephrostomy Catheter Set Recalled by Boston Scientific...
The Issue: Certain Malecot Nephrostomy Catheters are breaking at the mid-shaft bond...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Malecot Nephrostomy Catheter Set Recalled by Boston Scientific Corporation...
The Issue: Certain Malecot Nephrostomy Catheters are breaking at the mid-shaft bond...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity TF PET/CT (model 882442) running software version 4.0.2 This...
The Issue: A software issue causes PET reconstructions to fail intermittently. It was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: digital x-ray detector ProGrade R1 - solid state X ray Recalled by Philips...
The Issue: It the WiFi connection between the SkyPlate detector and HP transfer point...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synvisc-One ¿ (hylan G-F 20) Recalled by Sanofi Genzyme Due to Contamination...
The Issue: Contamination with Methylbacterium thiocyanatum
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific Guider Softip XF Guide Catheter Product Usage: Is Recalled...
The Issue: Potential polymer material degradation.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical Action Industries Inc. Blue OR Towel Non X-Ray Detectable Recalled...
The Issue: Product sterility potentially compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew Whipknot Soft Tissue Cinch #5 Sutures. PN: 7211015 Recalled...
The Issue: Packaging design is insufficient to prevent potential sterile barrier breach...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MHI-TM2000 Linear Accelerator System Product Usage: MHI-TM2000 Linear...
The Issue: Due to a system controller software anomaly, the patient positioning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARESCAPE R860 ventilators with software version 10SP05 Product Usage: The...
The Issue: Potential for the display processor to experience an unexpected failure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARCHITECT c4000 Cuvette Segment Recalled by Abbott Laboratories, Inc Due to...
The Issue: There is a potential to generate falsely depressed patient results in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARCHITECT c16000 Cuvette Segment Recalled by Abbott Laboratories, Inc Due to...
The Issue: There is a potential to generate falsely depressed patient results in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Humeral Stem 55mm(Size 13) Product Usage: Intended for primary and Recalled...
The Issue: Zimmer Biomet is conducting a medical device recall for two lots of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Humeral Stem 83mm(Size 17) Product Usage: Intended for primary and Recalled...
The Issue: Zimmer Biomet is conducting a medical device recall for two lots of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Remel Shigella sonnei Phase 1 & 2 Agglutinating Serum Recalled by Remel Inc...
The Issue: The serum may fail to agglutinate within the specified minimum reaction time.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARCHITECT c8000 Cuvette Segment Recalled by Abbott Laboratories, Inc Due to...
The Issue: There is a potential to generate falsely depressed patient results in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROPONENT SR Pacemaker Recalled by Boston Scientific Corporation Due to...
The Issue: Boston Scientific has received reports of intermittent over-sensing of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.