State

New York product recalls

73,806 recalls have nationwide distribution and so reach New York. 12,956 additional recalls listed New York specifically in their distribution scope.

What the numbers show

Total: 12,956
Critical: 1,508
Severe: 3,702
Most recent: 2026-11-04

Of the 12,956 recalls naming New York we have scored against our rubric, 1,508 (12%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 3,702 (29%) are Severe.

Which agencies issued them

These figures cover only the 12,956 recalls whose distribution notice names New York specifically. The 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

40751–40775 of 86762

SevereFDA (Drugs)·D-1022-2019·2019-03-27
Advanced Pharma Recalls Phenylephrine Syringes Due to Sterility Concerns
Advanced Pharma Inc. is recalling 1,575 syringes of Phenylephrine HCl injectable solution because the company cannot guarantee the product is sterile.
Product
Phenylephrine HCl, 400 mcg in 0.9% Sodium Chloride, QS 10 mL Injectable Solution 400 mcg/10 mL (40 mcg per mL), Sterile single use syringe, NDC: 42852-876-61 Avella of Houston 9265 Kirby Dr., Houston, TX 77054 (877) 794-0404
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1026-2019·2019-03-27
Advanced Pharma Recalls Lidocaine Syringes Due to Sterility Concerns
Advanced Pharma Inc. is recalling 1,540 syringes of 2% Lidocaine HCl Injectable Solution because the company cannot assure the product's sterility.
Product
2% Lidocaine HCl Injectable Solution, 60 mg/3 mL (20 mg per mL), 3mL Sterile single use syringe, NDC: 42852-011-22 Avella of Houston 9265 Kirby Dr., Houston, TX 77054 (877) 794-0404
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1039-2019·2019-03-27
Shimadzu Mobile X-Ray System Recalled for Brake Failure
Shimadzu is recalling 93 MobileDaRt Evolution mobile X-ray systems because the brakes may fail to engage when the operator releases the drive handle.
Product
SHIMADZU MobileDaRt Evolution (MX8 Version), Mobile X-Ray System Product Usage: This device is intended to be used to take a film, CR or general radiography of patients in the hospital who cannot move and/or of outpatients in emergency. Exposure can be captured on film, CR…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1065-2019·2019-03-27
Heritage Pharmaceuticals Recalls Subpotent Etomidate Injection Vials
Heritage Pharmaceuticals is recalling 11,888 vials of Etomidate Injection because the drug was found to be subpotent. The recall is voluntary and nationwide.
Product
Etomidate Injection, USP 20 mg/10mL (2mg/mL) 10 mL Single-Dose Vial, Rx only, Manufactured for: Heritage Pharmaceuticals Inc. Made in India, NDC 23155-160-31
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-1178-2019·2019-03-27
Horizon Food Group Recalls Ne-Mo's Red Velvet Cake Squares Due to Foreign Object
Horizon Food Group is recalling Ne-Mo's Red Velvet Cake Squares after a complaint of a bird foot found in the product.
Product
Ne-Mo's Red Velvet Cake Square with Cream Cheese Icing, item 408-6; Net Wt. 3 oz. Case UPC: 2007606404086 7 Display pk 6 ea/pk UPC: 10076064040860 0 Individual unit UPC: 07606400408 7 Frozen product has a shelf life of 365 days from the date of production Refrigerated…
Category
Food
Distribution
20 states
HighFDA (Devices)·Z-1040-2019·2019-03-27
Fujifilm FDR Go PLUS Mobile X-Ray System Recalled for Braking Defect
Fujifilm is recalling 56 mobile X-ray systems because the braking mechanism may fail to engage when the handle is released.
Product
Fujifilm FDR Go PLUS, Mobile X-Ray System Product Usage: This device is intended to be used to take a film, CR or general radiography of patients in the hospital who cannot move and/or of outpatients in emergency. Exposure can be captured on film, CR or Digital Radiography…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·19V240000·2019-03-27
Thor Motor Coach Recalls 2018-2020 Models Due to Reversed Backup Camera Image
Thor Motor Coach is recalling 110 motorhomes because the backup camera image may reverse, increasing crash risk. Dealers will install a harness to fix the issue.
Product
THOR MOTOR COACH — THOR MOTOR COACH FOUR WINDS, CHATEAU, MAGNITUDE, OMNI
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1036-2019·2019-03-27
ConvaTec Recalls Feeding Tubes Due to Potential Sterile Barrier Breach
ConvaTec is recalling specific lots of Feeding Tube Metric devices because an internal assessment found a potential breach in the sterile barrier.
Product
Feeding Tube Metric, disposable, sterile, 100 eaches per sales unit. Labeled as: xray CH05/40CM and xray CH08/40CM Product Usage: Duodenal and Stomach Gastroenterology Tubes are sterile disposable devices which may be inserted through the nose or mouth via the esophagus into…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1019-2019·2019-03-27
AAP Implantate Lambotte Chisel Recalled for Potential Breakage at Welded Parts
AAP Implantate AG is recalling 25 units of the 20 mm Lambotte chisel due to a potential risk of breaking at the welded piece parts of the chisel body and knocking plate.
Product
aap Implante AG, Lambotte chisel, 20 mm, REF IU 3000-20 Product Usage: Surgical instruments are intended to aid in the insertion of bone plates and screws as well as for reduction and support during orthopedic surgeries. If not otherwise specified, instruments are intended…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1021-2019·2019-03-27
Advanced Pharma Recalls Glycopyrrolate Syringes Due to Sterility Concerns
Advanced Pharma Inc. is recalling 2,580 syringes of Glycopyrrolate Injectable Solution nationwide due to a lack of assurance of sterility.
Product
Glycopyrrolate Injectable Solution 1 mg/5 mL (0.2 mg per mL), Sterile single use syringe, NDC: 42852-828-67 Avella of Houston 9265 Kirby Dr., Houston, TX 77054 (877) 794-0404
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·19V243000·2019-03-27
Osco Recalls Emergency Vehicles With Faulty Brake Light Wiring
Osco Tank & Truck Sales is recalling 16,342 emergency vehicles built on 2012 Kenworth T440 and 2018 Peterbilt 348 chassis because brake lights may illuminate without the pedal being pressed.
Product
KENWORTH — KENWORTH, PETERBILT T440, 348
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·19V244000·2019-03-27
Toyota Recalls 2019 Models Due to Illegible Load Capacity Labels
Toyota is recalling specific 2019 models because the load capacity label text may become illegible, potentially leading to vehicle overload and increased crash risk.
Product
TOYOTA — TOYOTA CAMRY, AVALON, PRIUS, RAV4
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·19V241000·2019-03-27
Volkswagen Recalls 2019 Tiguan LWB for Inaccurate Tire Information Label
Volkswagen is recalling 2019 Tiguan LWB vehicles because the tire information label contains inaccurate dimension and pressure specifications, which may increase crash risk.
Product
VOLKSWAGEN — VOLKSWAGEN TIGUAN
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Food)·F-1175-2019·2019-03-27
Jansal Valley Chocolate Covered Almonds Recalled for Undeclared Sesame
Friendly Fruit Market is recalling Jansal Valley Cocoa Dusted Chocolate Covered Almonds because the product contains undeclared sesame seeds.
Product
JANSAL VALLEY Cocoa Dusted Chocolate Covered Almonds, Net Weight: 6 OZ (170 G), packed in a plastic clamshell, UPC: 7 08152 32988 7
Category
Food
Distribution
8 states
HighFDA (Devices)·Z-1037-2019·2019-03-27
ConvaTec Recalls Nelaton Urinary Catheters Due to Sterile Barrier Breach Risk
ConvaTec is recalling Nelaton Urinary Catheters because an internal assessment found a potential breach in the sterile barrier, which could compromise the device's sterility.
Product
Nelaton Urinary Catheter, disposable, sterile, 100 eaches per sales unit. Labeled as: CH16/40CM and CH14/40CM Product Usage: Urinary Catheters are sterile disposable devices intended to provide an intermittent pathway for drainage of fluids from the bladder. They are…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1177-2019·2019-03-27
Horizon Food Group Recalls Ne-Mo's Chocolate Cake Squares Due to Foreign Object
Horizon Food Group is recalling Ne-Mo's Chocolate Cake Squares with Cream Cheese Icing after a complaint of a bird foot found in the product.
Product
Ne-Mo's Chocolate Cake Square with Cream Cheese Icing, item 104; Net Wt. 3 oz. Case UPC: 2007606401046 4; Display pk 6 ea/pk UPC: 10076064010460 7 Individual unit UPC: 07606400104 8 Frozen product has a shelf life of 365 days from the date of production Refrigerated…
Category
Food
Distribution
20 states
HighCPSC·19091·2019-03-27
Cambridge Elevating Recalls Home Elevators Due to Fall Hazard
Cambridge Elevating is recalling approximately 680 home elevators because the landing door can unlock without the elevator present, posing a fall hazard.
Product
Home elevators
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Food)·F-1179-2019·2019-03-27
Horizon Food Group Recalls Ne-Mo's Birthday Cake Squares Due to Foreign Object
Horizon Food Group is recalling Ne-Mo's Birthday Cake Squares with Buttercream Icing after a complaint that a bird foot was found in the product.
Product
Ne-Mo's Birthday Cake Square with Buttercream Icing, item 506-6; Net Wt. 3 oz. Case UPC: 2007606405066 8 Display pk 6 ea/pk UPC: 10076064050660 1 Individual unit UPC: 07606405066 4 Frozen product has a shelf life of 365 days from the date of production Refrigerated…
Category
Food
Distribution
20 states
HighFDA (Devices)·Z-1027-2019·2019-03-27
CP Medical Recalls Sterile Surgical Sutures Due to Potential Sterility Compromise
CP Medical Inc is recalling Plain and Chromic Gut Absorbable Surgical Sutures because routine endotoxin testing showed an out-of-limit result, potentially compromising sterility.
Product
Plain and Chromic Gut Absorbable Surgical Sutures, sterile. 12 sutures per box. Product Usage: Plain Gut Sutures are indicated for use in general soft tissue approximation and/or ligation, including use in ophthalmic procedures, but not for use in cardiovascular and neural…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1020-2019·2019-03-27
FDA Recalls 850 Units of Covidien Force TriVerse Electrosurgical Devices
The FDA is recalling 850 units of the Covidien Force TriVerse electrosurgical device due to potential sterile packaging compromise.
Product
Covidien Force TriVerse electrosurgical device 10 cord-Intended as electrosurgical energy to cut and/or coagulate tissue. Product Usage: Single-use device intended for use in open procedures (such as general, urologic, thoracic, plastic and reconstructive, gynecologic) and…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1015-2019·2019-03-27
Siemens Dimension Vista 1500 Analyzer Recall Due to Water Module Contamination
Siemens is recalling 5,373 Dimension Vista 1500 analyzers because specific water purification modules may cause falsely elevated triglyceride results.
Product
Dimension Vista 1500, Analyzer, chemistry Model no. 10444801
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1033-2019·2019-03-27
ACell Recalls Gentrix Surgical Matrix Thick Due to Tensile Strength Failure
ACell, Inc. is recalling one lot of Gentrix Surgical Matrix Thick because a sample failed to meet tensile strength specifications.
Product
Gentrix Surgical Matrix Thick, 20 x 30cm, Catalog Number PSMT2030, Lot 013948 - Product Usage: Gentrix Surgical Matrix Thick is intended for implantation to reinforce soft tissue where weakness exists in patients requiring gastroenterological or plastic and reconstructive…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1014-2019·2019-03-27
Siemens Dimension Vista 500 Analyzer Recall for Water Module Contamination
Siemens is recalling 5,373 Dimension Vista 500 analyzers because specific Millipore water purification modules may cause falsely elevated triglyceride results.
Product
Dimension Vista 500, Analyzer, chemistry Model no. 10284473
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1011-2019·2019-03-27
Akorn Recalls Hydrocortisone and Acetic Acid Otic Solution Due to Low Potency
Akorn Inc is recalling Hydrocortisone and Acetic Acid Otic Solution because routine stability testing revealed the drug was sub-potent.
Product
Hydrocortisone and Acetic Acid Otic Solution, USP, 10 mL per dropper bottle, Rx only, Hi-Tech Pharmacal Co, Inc., Amityville, NY 11701. NDC: 50383-901-10
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1038-2019·2019-03-27
ConvaTec Recalls FilterFlow Suction Handles Due to Sterile Barrier Breach Risk
ConvaTec is recalling 124,000 FilterFlow Suction Handles because an internal assessment found a potential breach in the sterile barrier.
Product
FilterFlow Suction Handle CH24, 20 eaches per sales unit. Product Usage: Filter Flow is designed for orthopedic surgery and combines suctioning function with filtering. The device is intended for orthopedic surgical procedures to remove and collect debris and bone fragments…
Category
Medical Device
Distribution
Distributed nationwide