Recalls distributed in New York
These notices name New York in the distribution list the company gave its agency. That list says where the product was shipped, not where it ended up — a recalled item can travel with a shopper, and some notices list no states at all.
6,374 stored notices name New York, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach New York too — those are in the archive.
Reported Jun 17, 2026
NeoSpan¿ SuperElastic Compression Staple w/Instruments Catalog Number and Product Name T50 SN010 NeoSpan¿ SuperElastic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.In2bones USA, LLC
FDA (openFDA device enforcement)
Reported Jun 17, 2026
Brand Name: CGuard¿ Prime Carotid Stent System, 135cm, 8mmx30mm Model/Catalog Number: CND0830
Moderate riskThis product could cause temporary or reversible health problems — stop using it.INSPIREMD Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 17, 2026
Individual Unit Label (both lid and front of cup): Whole Foods Market Kitchens Minestrone Soup, VEGETARIAN NET WT 24 OZ…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Kettle Cuisine, LLC
FDA (openFDA food enforcement)
Reported Jun 17, 2026
Farm Rich Pizza Cheese Crunchers
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Rich Products Corp.
FDA (openFDA food enforcement)
Reported Jun 17, 2026
NexxZr T Multi A3.5 W98-16mm, REF: 745451
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sagemax Bioceramics, Inc.
FDA (openFDA device enforcement)
Reported Jun 10, 2026
Brand Name: Exacta Mix Product Name: Vented Micro-Volume Inlet Model/Catalog Number: H938175 Product Description:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
FDA (openFDA device enforcement)
Reported Jun 10, 2026
Avanta Multi-Patient Administration Tube Sets (AVA 500 MPAT (Part 2 of 2)) used with the Medrad¿ Avanta Injection…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bayer Medical Care, Inc.
FDA (openFDA device enforcement)
Reported Jun 10, 2026
BD¿Spinal Tray with BD¿Quincke Needle 22 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Becton Dickinson & Company
9 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 10, 2026
Atlan A350. Model Number: 8211500. anesthesia workstation
High riskUsing this product could cause serious injury, illness or death — stop using it now.Draeger, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 10, 2026
Birch Benders Sweet Potato Pancake and Waffle Mix 12oz bag, UPC 8 1000156076 8, 6 bags per case
High riskUsing this product could cause serious injury, illness or death — stop using it now.Hometown Food Company
FDA (openFDA food enforcement)
Reported Jun 10, 2026
Brand Name: Da Vinci 5 Product Name: ASSY,DV5 TOWER,IS5000 Model/Catalog Number: 380746 Software Version: N/A Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
FDA (openFDA device enforcement)
Reported Jun 10, 2026
#007560 Fiery Hot Seasoning (Reduced Salt), Net Wt: 25 lbs. JCB Flavors, 1224 Clark Street, Watertown, WI 53094
High riskUsing this product could cause serious injury, illness or death — stop using it now.JCB Flavors, LLC
9 more products in this recall
FDA (openFDA food enforcement)
Reported Jun 10, 2026
Arvis Hip & Knee 3.0 Instrument Set, REF: IN-28000 containing one of the following components: IN-10500, Impactor…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kico Knee Innovation Company
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 10, 2026
PhaseOne Antimicrobial Solution, Model/Catalog Number: 15050
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Oculus Technologies
FDA (openFDA device enforcement)
Reported Jun 10, 2026
Digital Angiography System Trinias:UD150G-40 / D150GC-40; Digital Angiography System BRANSIST safire:UD150G-40 /…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Shimadzu Medical Systems
FDA (openFDA device enforcement)
Reported Jun 10, 2026
Hellas Meze Golden Smoked Whole Herring
High riskUsing this product could cause serious injury, illness or death — stop using it now.Terra Medi LLC
FDA (openFDA food enforcement)
Reported Jun 10, 2026
1) Cheese Sauce Mix, 25.5 oz., packaged in a sealed poly bag and packed 12 bags per case, UPC 0399549125016 2) Cheese…
High riskUsing this product could cause serious injury, illness or death — stop using it now.The Coffee Connexion Co., Inc.
3 more products in this recall
FDA (openFDA food enforcement)
Reported Jun 10, 2026
Raw Shelled Peanuts (Runner Type) 2,200 lb. Poly Tote Bags and 50kg Poly Bags
High riskUsing this product could cause serious injury, illness or death — stop using it now.Wilco Peanut Co.
FDA (openFDA food enforcement)
Reported Jun 3, 2026
Automated Impella Controller (AIC); Product Code: 0042-0000-US;
High riskUsing this product could cause serious injury, illness or death — stop using it now.Abiomed, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 3, 2026
Halyard Purezero Ultraviolet Nitrile Exam Gloves Reference Numbers: 48771 (XS), 48772 (Sm.), 48773 (Md.), 48774 (Lg.),…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.O&m Halyard Inc.
FDA (openFDA device enforcement)
Reported May 27, 2026
Swan-Ganz Catheter, Models: 131F7/131F7P, 131F7J, 141F7, 151F7, 834F75, 096F6/096F6P, C144F7, 782F75M, 132F5, C146F7,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton, Dickinson and Company
2 more products in this recall
FDA (openFDA device enforcement)
Reported May 27, 2026
Silastic Foley Catheters Silastic Brand Foley Catheter 30cc REF: 33416 33418 33420 33422 33424 Silastic Brand Foley…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.C.R. Bard Inc.
FDA (openFDA device enforcement)
Reported May 27, 2026
GHIRARDELLI PERFECTLY PREMIUM FRAPPE MIX FROZEN HOT COCOA NET WT 50oz (3lbs 2oz) 1.42kg Ingredients: *** nonfat dry…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Ghirardelli Chocolate Company
9 more products in this recall
FDA (openFDA food enforcement)
Reported May 27, 2026
Oncology Kit w/60" (152 cm) Appx 2.2 ml, Smallbore Ext Set w/ChemoLock Port, Clamp, Anti-Siphon Valve, Spiros;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical, Inc.
FDA (openFDA device enforcement)
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Other states
RecallNow is not a government agency. Every notice above was published by the FDA, USDA FSIS or CPSC and links back to its source. Browse the whole archive.