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. 2,763 recalls have been distributed to New York in the last 12 months.
Showing 17081–17100 of 30,153 recalls
Recalled Item: Single-Lumen Central Venous Catheterization Kit with Blue FlexTip(R)...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NvisionVLE¿ Low-Profile Optical Probe Recalled by Ninepoint Medical Inc. Due...
The Issue: Distal tips of the probes may detach from the probe shaft during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Angio-Seal Evolution Vascular Closure Device Recalled by Terumo Medical Corp...
The Issue: Two lots of product were released for distribution prior to the completion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HLD Systems 600 Series Washer/Pasteurizer Recalled by Cenorin, LLC Due to...
The Issue: There is a supplier quality issue with the terminal blocks which may cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VGI MEDICAL VerteLP LATERAL INTERBODY FUSION instrument kit Recalled by VGI...
The Issue: IFU contained an automated cleaning process for the VerteLP Instrument Tray...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: smith&nephew 5o (5 degree) GENESIS(R) II VALGUS BUSHING Recalled by Smith &...
The Issue: A single lot of GENESIS II FEMORAL FIVE DEGREE VALGUS BUSHING due to a laser...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EEA" Hemorrhoid and Prolapse Stapler Set with DST Series" Technology 3.5MM...
The Issue: There is a potential for improper welding of the yellow staple guide to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EEA" Hemorrhoid and Prolapse Stapler Set with DST Series" Technology 4.8MM...
The Issue: There is a potential for improper welding of the yellow staple guide to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DriSate¿ Product Code DR-145 The acid concentrate powders and liquids...
The Issue: A subassembly component (dextrose bag) within this case product contained...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OviTex 1S Reinforced BioScaffold 4x8cm Recalled by AROA Biosurgery, LTD. Due...
The Issue: Degradation of the PGA suture material used in the manufacture of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OviTex Reinforced BioScaffold 6x10cm Recalled by AROA Biosurgery, LTD. Due...
The Issue: Degradation of the PGA suture material used in the manufacture of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OviTex 2S Reinforced BioScaffold 10x12cm Recalled by AROA Biosurgery, LTD....
The Issue: Degradation of the PGA suture material used in the manufacture of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OviTex 1S Reinforced BioScaffold 10x12cm Recalled by AROA Biosurgery, LTD....
The Issue: Degradation of the PGA suture material used in the manufacture of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OviTex 2S Reinforced BioScaffold 18x22cm Recalled by AROA Biosurgery, LTD....
The Issue: Degradation of the PGA suture material used in the manufacture of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OviTex Reinforced BioScaffold 10x20cm Recalled by AROA Biosurgery, LTD. Due...
The Issue: Degradation of the PGA suture material used in the manufacture of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OviTex 2S Reinforced BioScaffold 10x12cm Recalled by AROA Biosurgery, LTD....
The Issue: Degradation of the PGA suture material used in the manufacture of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OviTex 2S Reinforced BioScaffold 16x20cm Recalled by AROA Biosurgery, LTD....
The Issue: Degradation of the PGA suture material used in the manufacture of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OviTex 2S Reinforced BioScaffold 10x20cm Recalled by AROA Biosurgery, LTD....
The Issue: Degradation of the PGA suture material used in the manufacture of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OviTex 1S Reinforced BioScaffold 20x20cm Recalled by AROA Biosurgery, LTD....
The Issue: Degradation of the PGA suture material used in the manufacture of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OviTex Reinforced BioScaffold 4x8cm Recalled by AROA Biosurgery, LTD. Due to...
The Issue: Degradation of the PGA suture material used in the manufacture of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.