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 48,132 notices were distributed nationwide, so they reach New York too — those are in the archive.
Reported Apr 13, 2016
GE Inspection Technologies, LP, Cabinet X-ray system used for industrial quality control.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Inspection Technologies, LP
FDA (openFDA device enforcement)
Reported Apr 13, 2016
Chef Hon brand STEAMED BUNS WITH SEAFOOD & VEGETABLE, Net Wt. 1 lb. 8 oz. (682g), UPC 7 47518 00156 2, Product Code #…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Peking Food LLC
1 more product in this recall
FDA (openFDA food enforcement)
Reported Apr 13, 2016
Richard-Allan Scientific Paraffin Type 3 For in vitro diagnostic use. For use as an infiltration and embedding medium…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Richard-Allan Scientific Company
FDA (openFDA device enforcement)
Reported Apr 13, 2016
TeleSentry Battery, 3.7 Li-Ion Polymer Battery, CAUTION Do not expose to high temperature. Do not disassemble. Dispose…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Scottcare Corporation
FDA (openFDA device enforcement)
Reported Apr 13, 2016
A Picture Archiving and Communication System (PACS) intended to display, process, read, report, communicate,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Apr 13, 2016
Titanium Low Profile Neuro Screw, Self Drilling, 3mm, part numbers: 400.833, 400.833E Product Usage: The Low Profile…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes (USA) Products LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 13, 2016
The THERAKOS CELLEX Photopheresis System is a photoimmune therapy. Catalog CLXUSA. Manufacturing lot D342 UDI:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Therakos Inc.
FDA (openFDA device enforcement)
Reported Apr 13, 2016
Guardian II Hemostasis Valve, models 8210 and 8211. The following models are only available Outside the US: FH101,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Vascular Solutions, Inc.
FDA (openFDA device enforcement)
Reported Apr 13, 2016
Persona The Personalized Knee System Articular Surface Posterior Stabilized (PS) Left Height 14mm Sterile. For use in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Manufacturing B.V.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 12, 2016
Mountain Products Inc. Retira Productos De Carne De Cerdo Por Error De Rotulacin Y Alergenos No Declarados
High riskUsing this product could cause serious injury, illness or death — stop using it now.Mountain Products Inc.
USDA FSIS
Reported Apr 6, 2016
The Spectra-System Dental Implant 2008 system is comprised of dental implant fixtures and prosthetic devices that…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Implant Direct Sybron Manufacturing, LLC
FDA (openFDA device enforcement)
Reported Apr 6, 2016
VERO MHI-TM2000 Linear Accelerator System --- Common Name: Medical Linear Accelerator MHI-TM2000 Linear Accelerator…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mitsubishi Heavy Industries, Ltd., Hiroshima Machinery Work
FDA (openFDA device enforcement)
Reported Apr 6, 2016
MAGGI Chicken Flavor Bouillon 6Tab, 12Tab UPC Codes: 028000247959, 028000115678, 028000115678
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nestle USA
1 more product in this recall
FDA (openFDA food enforcement)
Reported Apr 6, 2016
Knee Shield (Patella Cup) Product Usage: Knee Shield patella cup is an accessory used with the knee braces to provide…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ossur H / F
13 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 6, 2016
Thai Fusion Outpost, net weight 5.1 oz. UPC 0 99853 34255 9. Thai Fusion Bulk bag, packaged in a ziploc plastic bag,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Paradise Farm Organics Inc.
FDA (openFDA food enforcement)
Reported Apr 6, 2016
Helios HL3T and HLT Track Mounted Dental Lights Product Usage: The product is intended for use by dental professionals…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pelton & Crane / Marus / DCI Equipment / KaVo
FDA (openFDA device enforcement)
Reported Apr 6, 2016
The S.C.O.R.E.S. Unit (self contained operating room equipment sterilization unit)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pmbs, LLC
FDA (openFDA device enforcement)
Reported Apr 6, 2016
Phenobarbital/Hyoscyamine/ Atropine/Scopolamine 16.2/0.1037/0.0194/0.0065 mg DONNATAL ELIXIR, 5 ml Cup grape, Alcohol…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Safecor Health, LLC
FDA (openFDA drug enforcement)
Reported Apr 6, 2016
The E.CAM gamma camera system Product Usage: The E.CAM gamma camera system is a SPECT system and measures the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 6, 2016
Cios Alpha, mobile X-ray system
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
15 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 6, 2016
Synthes Interlocking Bolt, 151 mm (General and Plastics Surgery Devices) Guide, Surgical Instrument
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes (USA) Products LLC
FDA (openFDA device enforcement)
Reported Apr 6, 2016
Clear Vue Prone Breast Treatment Table and Access ClearVision Prone Breast Device Product Usage: Clear Vue Prone Breast…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Wfr/aquaplast Corp.
FDA (openFDA device enforcement)
Reported Mar 30, 2016
Arthrex IBalance TKA Tibial Tray Size 2 - Catalog # AR-503-TTTC, Size 3 - Catalog # AR-503-TTTD, Size 4 -Catalog #…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arthrex, Inc.
FDA (openFDA device enforcement)
Reported Mar 30, 2016
Alaris PC Unit, Infusion Pump Model 8000, Part No. TC10005092
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CareFusion 303, 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.