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.
6,478 stored notices name New York, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,853 notices were distributed nationwide, so they reach New York too — those are in the archive.
Reported Mar 7, 2018
SOUTHERN GROVE ALMONDS Unsalted 14 oz (397g) pouch bag INGREDIENTS: ALMONDS. Distributed by ALDI Inc. Batavia, IL 60510…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kanan Enterprises, Inc.
FDA (openFDA food enforcement)
Reported Mar 7, 2018
Max Implant System - Bone Tap for use with 7.0mm diameter Max Implant, Catalog Number D-TAP-MAX7-7 Dental implants are…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Keystone Dental Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 7, 2018
M&P Food Productions brand Vareniki, Potato and Mushroom, Net Wt. 14 oz. (396 g), Keep Frozen, UPC: 7 07163 02617 4
Moderate riskThis product could cause temporary or reversible health problems — stop using it.M & P Food Productions, Ltd.
6 more products in this recall
FDA (openFDA food enforcement)
Reported Mar 7, 2018
MEDISTIM VERIQ SYSTEM, MODEL VQ4122 An intraoperative diagnostic system that utilizes ultrasonography to guide surgeons…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medistim Asa
FDA (openFDA device enforcement)
Reported Mar 7, 2018
AIRO Mobile CT System, Model Number: MobiCT-32 Product Usage: The AIRO¿ is intended to be used for X-ray computed…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mobius Imaging, LLC
FDA (openFDA device enforcement)
Reported Mar 7, 2018
OTTO BOCK Kenevo knee joints Model 3C60
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Otto Bock Healthcare Product
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 7, 2018
BNS WHEAT ROLLS ( Under the following Trade Names - Giant, Harvest Pride, Shoppers and Old Tyme )
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Schmidt Baking Co., Inc.
25 more products in this recall
FDA (openFDA food enforcement)
Reported Mar 7, 2018
Seggiano Artichoke & Garlic Sauce & Spread Net Weight 200g, 7.1 oz, packaged in Glass jar, UPC Code: 812603020381
High riskUsing this product could cause serious injury, illness or death — stop using it now.Seggiano USA Inc.
FDA (openFDA food enforcement)
Reported Mar 7, 2018
ST AIA-PACK¿ PROG II, Progesterone II Assay, Part Number: 025239
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tosoh Bioscience Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 7, 2018
Zimmer Segmental System, ZSS Distal Femur. Sizes as follows: a. Size B-LT (Item No. 00585001201); b. Size B-RT (Item…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 28, 2018
Innova Self-Expanding Stent System, 200 mm. Labeled with Material Number and description as follows: Product Usage: The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 28, 2018
Custom sterile surgical packs labeled as follows: GEO-MED CABG PACK PGYBK A & B, REF 89-5985.07, STERILE EO Use:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DeRoyal Industries Inc.
FDA (openFDA device enforcement)
Reported Feb 28, 2018
Flexfrost Protein Ice Cream Chocolate Flexfrost L.L.C. 622 RT 10 Whippany, NJ 07981
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Flexfrost
4 more products in this recall
FDA (openFDA food enforcement)
Reported Feb 28, 2018
Pentax Video Duodenoscope Model: ED-3490TK (UDI of design being recalled: 04961333232420) These instruments are…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pentax
FDA (openFDA device enforcement)
Reported Feb 28, 2018
Cobas 8000 Modular Series system; Software Version 05-02 and 06-03; UDI: 05641446001
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Corporation
FDA (openFDA device enforcement)
Reported Feb 28, 2018
ROSA Brain 3.0 Stereotaxic instrument Computer-assisted surgical device. Intended for the spatial positioning and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 21, 2018
A & A Finest Retira Productos De Albndiga De Cerdo Y Camarones Congelados Debido A Un Error De Rotulacin Y Un Alrgeno…
High riskUsing this product could cause serious injury, illness or death — stop using it now.A & A Finest
USDA FSIS
Reported Feb 21, 2018
AVID Medical QA Pack AV10654-10
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Avid Medical, Inc.
FDA (openFDA device enforcement)
Reported Feb 21, 2018
Lyophilized Chemistry Calibrator Level 1 Product Usage: Beckman Coulter Chemistry Calibrators are intended for use when…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
FDA (openFDA device enforcement)
Reported Feb 21, 2018
WALNUT CREEK FOODS Caramel Popcorn NET WT 15 OZ (425g) Ingredients: Evaporated Can Juice, Popcorn, Butter (cream,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Coblentz Distributing Inc. dba Walnut Creek Foods
FDA (openFDA food enforcement)
Reported Feb 21, 2018
Central Venous Catheter Set Triple Lumen Polyurethane, Catalog Identifier: C-UTLM-501J Product Usage: The central…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cook Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 21, 2018
Carestation 620 A1, Carestation 650 A1, and Carestation 650c A1
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Medical Systems China Co., Ltd.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 21, 2018
Lemon Ginger Syrup, packaged in 100 mL or 250 mL glass bottle. 100 mL bottle has UPC 8 53142 00504 0. 250 mL bottle has…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Improper Goods
1 more product in this recall
FDA (openFDA food enforcement)
Reported Feb 21, 2018
Vado Steerable Sheath 8.8F, REF SS8FMU67, packaged in a lidded tray that is within a pouch which is inserted into a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kalila Medical
1 more product in this recall
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.