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. 1,914 recalls have been distributed to New York in the last 12 months.
Showing 31561–31580 of 55,896 recalls
Recalled Item: Rugby Diocto Liquid Recalled by The Harvard Drug Group Due to Microbial...
The Issue: Microbial contamination of Non-sterile Products; presence of yeast and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rugby Aller-chlor (Chlorpheniramine Maleate Syrup Recalled by The Harvard...
The Issue: Microbial contamination of Non-sterile Products; presence of yeast and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rugby Senexon Liquid Natural Vegetable Stimulant Recalled by The Harvard...
The Issue: Microbial contamination of Non-sterile Products; presence of yeast and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Major Senna Syrup Natural Vegetable Laxative Recalled by The Harvard Drug...
The Issue: Microbial contamination of Non-sterile Products; presence of yeast and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: The OriGen Reinforced Dual Lumen catheter (RDLC) is a duel Recalled by...
The Issue: Two users have reported to OriGen that a VV28F OriGen Reinforced Dual Lumen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JANUS & JANUS G3 Automated Workstation is an automated programmable Recalled...
The Issue: We have become aware through internal testing that JANUS and Janus G3...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemosll ReadiPlasTin (20 ml Size) Recalled by Instrumentation Laboratory Co....
The Issue: Instrumentation Laboratory Co. received customer reports of performance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Presource(R) Kits (custom surgical/procedural kits): The standard and custom...
The Issue: The firm manufactured and distributed Presource(R) kits which contained BD...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Versys 6 inch Beaded Full Coat Plus Hip Prosthesis. Labeled Recalled by...
The Issue: The products being recalled exceeded the weight previously tested leading to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Segmental System Recalled by Zimmer Biomet, Inc. Due to The products...
The Issue: The products being recalled exceeded the weight previously tested leading to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NATURAL HERBAL COFFEE AMPT Recalled by The Ampt Life, LLC Due to Undeclared...
The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis found the product to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Friendly Farms Key Lime Crunch Tilts Greek Lowfat Yogurt Recalled by...
The Issue: Recalling Friendly Farms Key Lime Crunch Tilts because it may contain...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 125" (318 cm) Y-Type Blood Set w/170 Micron Filter Recalled by ICU Medical,...
The Issue: Some devices were labeled as Does not contain DEHP even though the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Foot Controls impacted for the following devices: OAKWORKS¿ Medical CFPM...
The Issue: The foot control used on the OAKWORKS¿ Inc., CFPM300, CFPM301, CFPM400,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 140" (356 cm) Y-Type Blood Set w/170 Micron Filter Recalled by ICU Medical,...
The Issue: Some devices were labeled as Does not contain DEHP even though the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 88" (224 cm) 20 Drop Y-Type Blood Set w/200 Micron Filter Recalled by ICU...
The Issue: Some devices were labeled as Does not contain DEHP even though the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 120" (305 cm) 10 Drop Primary Set w/2 MicroClave¿ Recalled by ICU Medical,...
The Issue: Some devices were labeled as Does not contain DEHP even though the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lopez Valve¿ w/Red Cap Recalled by ICU Medical, Inc. Due to Some devices...
The Issue: Some devices were labeled as Does not contain DEHP even though the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 132" (335 cm) Y-Type Admin Set w/170 Micron Blood Filter Recalled by ICU...
The Issue: Some devices were labeled as Does not contain DEHP even though the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 99" (251 cm) 20 Drop Y-Type Blood Set w/200 Micron Filter Recalled by ICU...
The Issue: Some devices were labeled as Does not contain DEHP even though the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.