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. 2,659 recalls have been distributed to New York in the last 12 months.
Showing 28461–28480 of 30,153 recalls
Recalled Item: NEUROPATH 6Fx90 GUIDING CATH S2 Product Code: GSM60900000 Intended for...
The Issue: Sterility of device may be compromised due to lack of package integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Multi-Vector Distractor - Multi-axial Mandible Distractor (Left)...
The Issue: It was discovered that the sheer pin on the Multi-Vector Distractor may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEUROPATH 5Fx100 GUIDING CATH MC Product Code: GCB51000000 Intended for...
The Issue: Sterility of device may be compromised due to lack of package integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Dens Instrument Set (Dens Graphic Case) Recalled by Synthes USA HQ,...
The Issue: The Dens Instrument Set has been designed to facilitate the anterior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEUROPATH 5Fx100 GUIDING CATH MP Product Code:GMD51000000 Intended for use...
The Issue: Sterility of device may be compromised due to lack of package integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEUROPATH 5Fx90 GUIDING CATH MPD Product Code: GMD50900000 Intended for...
The Issue: Sterility of device may be compromised due to lack of package integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEUROPATH 5Fx100 GUIDING CATH HH Product Code: GHH51000000 Intended for...
The Issue: Sterility of device may be compromised due to lack of package integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEUROPATH 6Fx90 GUIDING CATH MCV Product Code: GCB60900000 Intended for...
The Issue: Sterility of device may be compromised due to lack of package integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Multi-Vector Distractor Recalled by Synthes USA HQ, Inc. Due to It...
The Issue: It was discovered that the sheer pin on the Multi-Vector Distractor may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Multi-Vector Distractor Body Recalled by Synthes USA HQ, Inc. Due to...
The Issue: It was discovered that the sheer pin on the Multi-Vector Distractor may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Titanium Midface Distractor Recalled by Synthes USA HQ, Inc. Due to...
The Issue: There is the potential for the anterior footplates to not fit onto the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Large Combination Clamp/Large External Fixation System Recalled by Synthes...
The Issue: The L1 hex nuts, used to tighten the Large Combination Clamp, were oversized...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEUROPATH 6Fx90 GUIDING CATH HH Product Code: GHH60900000 Intended for...
The Issue: Sterility of device may be compromised due to lack of package integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ventri Discovery NM 530c Recalled by GE Healthcare, LLC Due to GE Healthcare...
The Issue: GE Healthcare has recently become aware of an incident which caused a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Giraffe OmniBed¿ and Giraffe Incubator p/n 6600-0723-700 (rev A and Recalled...
The Issue: Neonatal beds and incubator display boards may randomly overwrite stored...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SeriScaffold Surgical Scaffold Product Number: SCF10X25AGEN. Surgical mesh...
The Issue: Product is dual packaged in an inner and outer pouch, the outer pouch seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns flexible arterial cannula Recalled by Terumo Cardiovascular Systems...
The Issue: Flexible Arterial Cannula and High-Flow Aortic Arch Cannula connectors were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns high-flow aortic arch cannula Recalled by Terumo Cardiovascular...
The Issue: Flexible Arterial Cannula and High-Flow Aortic Arch Cannula connectors were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns high-flow aortic arch cannula Recalled by Terumo Cardiovascular...
The Issue: Flexible Arterial Cannula and High-Flow Aortic Arch Cannula connectors were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns flexible arterial cannula Recalled by Terumo Cardiovascular Systems...
The Issue: Flexible Arterial Cannula and High-Flow Aortic Arch Cannula connectors were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.