State

New York product recalls

73,741 recalls have nationwide distribution and so reach New York. 12,955 additional recalls listed New York specifically in their distribution scope.

What the numbers show

Total: 12,955
Critical: 1,508
Severe: 3,701
Most recent: 2026-10-28

Of the 12,955 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 3,701 (29%) are Severe.

Which agencies issued them

These figures cover only the 12,955 recalls whose distribution notice names New York specifically. The 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

36026–36050 of 86696

SevereFDA (Devices)·Z-0610-2020·2019-12-18
Smiths Medical Medfusion 4000 Syringe Pump Firmware Recall
Smiths Medical is recalling 626 Medfusion 4000 Syringe Pumps due to a firmware anomaly that may disable battery alarms and interrupt therapy.
Product
Medfusion Syringe Pump, Model 4000. The Model 4000 pump is a small, lightweight and portable syringe infusion pump. The pump offers a variety of delivery modes programmable to meet specific patient care needs.
Category
Medical Device
Distribution
3 states
SevereFDA (Drugs)·D-0620-2020·2019-12-18
SCA Pharmaceuticals Recalls Lidocaine Syringes Due to Foreign Material
SCA Pharmaceuticals is recalling Lidocaine HCl 2% syringes because foreign material was found inside the vials.
Product
Lidocaine HCl 2% 5 mL, Syringe, Rx Only, SCA Pharmaceuticals 755 Rainbow Road Windsor, CT 08695 NDC 70004-0723-09
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0587-2020·2019-12-18
Cook CrossCath Support Catheter Recall Due to Manufacturing Error
Cook Inc. is recalling 20 CrossCath Support Catheters because a manufacturing error may cause radiopaque marker bands to be too loose or too tight.
Product
CrossCath Support Catheter, RPN CXC3.0-1.9-14-90-P-NS-0, Order Number G51572 For diagnostic and interventional vascular procedures.
Category
Medical Device
Distribution
20 states
SevereFDA (Food)·F-0238-2020·2019-12-18
Cain Food Industries Recalls Vitamin D2 Blend Due to Salmonella Risk
Cain Food Industries is recalling 2,000 pounds of Vitamin D2 Blend due to possible Salmonella contamination. The product was distributed in seven states.
Product
Vitamin D2 Blend packaged in 50 lb. Multi-wall paper bag with polyethylene liner bags
Category
Food
Distribution
7 states
SevereFDA (Drugs)·D-0590-2020·2019-12-18
Anazao Health Recalls Hydromorphone, Baclofen, and Clonidine Combination Drugs
Coast Quality Pharmacy, LLC dba Anazao Health is recalling Hydromorphone HCL, Baclofen, and Clonidine HCL combination drugs due to fungal contamination found during environmental sampling.
Product
Hydromorphone HCL and Baclofen and Clonidine HCL in all strengths, all doses and all packaging, AnazaoHealth 5710 Hoover Blvd Tampa, FL 33634.
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·19V901000·2019-12-18
Forest River Recalls 2020 Motorhomes Due to Trailer Hitch Bolt Issue
Forest River is recalling 2020 Georgetown and FR3 motorhomes because improperly tightened trailer hitch bolts may loosen, increasing crash risk.
Product
FOREST RIVER — FOREST RIVER GEORGETOWN, FR3
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0636-2020·2019-12-18
AuroMedics Recalls Mirtazapine Tablets Due to Labeling Error
AuroMedics Pharma LLC is recalling Mirtazapine 15 mg tablets because some 500-count bottles are incorrectly labeled as 7.5 mg tablets.
Product
MIRTAZAPINE — MIRTAZAPINE (MIRTAZAPINE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0589-2020·2019-12-18
Cook Inc. Recalls CrossCath Support Catheters Due to Manufacturing Error
Cook Inc. is recalling 43 CrossCath Support Catheters because a manufacturing error may cause radiopaque marker bands to be too loose or too tight.
Product
CrossCath Support Catheter, RPN CXC3.4-2.2-18-135-P-NS-0, Order Number G51583 For diagnostic and interventional vascular procedures.
Category
Medical Device
Distribution
20 states
SevereFDA (Devices)·Z-0590-2020·2019-12-18
Cook Inc. Recalls CrossCath Support Catheters Due to Marker Band Fit Issues
Cook Inc. is recalling 58 CrossCath Support Catheters because a manufacturing error may cause radiopaque marker bands to be too loose or too tight.
Product
CrossCath Support Catheter, RPN CXC3.4-2.2-18-150-P-NS-0, Order Number G51577 For diagnostic and interventional vascular procedures.
Category
Medical Device
Distribution
20 states
SevereFDA (Devices)·Z-0675-2020·2019-12-18
Cognision Subject Kit Recalled for Potential B. cepacia Contamination
Neuronetrix Solutions is recalling 3,108 units of the Cognision Subject Kit (Clinical Grade) due to potential contamination with Burkholderia cepacia.
Product
Cognision, Subject Kit (Clinical Grade), Model 3000- containing Hydro Dot brand Wave Prep cups-electroconductive cream for use with external electrodes. Order No. D5000, Part No. PN-1720 - Product Usage: An electroconductive cream for use with external electrodes to reduce the…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0599-2020·2019-12-18
Anazao Health Recalls Compounded Sufentanil Syringes Due to Fungal Contamination
Coast Quality Pharmacy, LLC dba Anazao Health is recalling compounded sufentanil, clonidine, and bupivacaine syringes because environmental sampling detected Talaromyces rotundus.
Product
Sufentanil Citrate PF 90 mcg/mL/Clonidine HCL PF 500 mcg/mL/Bupivacaine HCL PF 12.8 mg/mL, Compounded, 20 mL Syringe, AnazaoHealth 5710 Hoover Blvd Tampa, FL 33634.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0587-2020·2019-12-18
Anazao Health Recalls Fentanyl and Morphine Compounded Drugs Due to Fungal Contamination
Anazao Health is recalling compounded fentanyl and morphine drugs after environmental sampling detected Talaromyces rotundus fungi.
Product
Fentanyl Citrate and Bupivacaine HCl and Morphine Sulfate in all strengths, all doses and all packaging, AnazaoHealth 5710 Hoover Blvd Tampa, FL 33634.
Category
Drug
Distribution
Distributed nationwide
SevereUSDA FSIS·120-2019·2019-12-18
Montpak Recalls Veal and Lamb Products Lacking Import Inspection
Montpak International Inc. is recalling approximately 4,365 pounds of veal and lamb products that were imported into the U.S. without the benefit of import re-inspection.
Product
Montpak International Inc. Recalls Veal and Lamb Products Produced Without Benefit of Import Inspection
Category
Food
Distribution
3 states
SevereFDA (Food)·F-0330-2020·2019-12-18
Breakstones Cottage Cheese Recalled for Potential Plastic and Metal Contamination
Kraft Heinz is recalling Breakstones 4% Milkfat Small Curd Cottage Cheese due to the potential presence of red plastic and metal pieces introduced during production.
Product
Breakstones 4% Milkfat Small Curd Cottage Cheese, in 24 oz. Plastic Tub, with UPC 0 21000 12284 4, 12 packages per case
Category
Food
Distribution
Distributed nationwide
SevereCPSC·20041·2019-12-18
Hillsdale Furniture Recalls Five-Drawer Chests Due to Tip-Over and Entrapment Hazards
Hillsdale Furniture is recalling Chadwick and Bailey five-drawer chests because they can tip over or entrap children if not anchored to the wall.
Product
Chadwick and Bailey five-drawer chests
Category
Consumer Product
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0602-2020·2019-12-18
Anazao Health Recalls Baclofen, Clonidine, and Morphine Sulfate Due to Fungal Contamination
Anazao Health is recalling Baclofen, Clonidine HCL, and Morphine Sulfate products due to the detection of Talaromyces rotundus fungi during environmental sampling.
Product
Baclofen and Clonidine HCL and Morphine Sulfate in all strengths, all doses and all packaging, AnazaoHealth 5710 Hoover Blvd Tampa, FL 33634.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0608-2020·2019-12-18
FDA Recalls Anazao Health Hydromorphone, Clonidine, and Fentanyl Combination Drugs
Anazao Health is recalling specific lots of hydromorphone, clonidine, and fentanyl combination drugs due to fungal contamination found during environmental sampling.
Product
Hydromorphone HCL and Clonidine HCL and Fentanyl Citrate in all strengths, all doses and all packaging, AnazaoHealth 5710 Hoover Blvd Tampa, FL 33634.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-0242-2020·2019-12-18
Cain Food Industries Recalls CDC-2010 Due to Salmonella Contamination Risk
Cain Food Industries is recalling 600 pounds of CDC-2010 packaged in 50 lb. bags due to possible Salmonella contamination. The product was distributed in seven states.
Product
CDC-2010 packaged in 50 lb. Multi-wall paper bag with polyethylene liner
Category
Food
Distribution
7 states
SevereFDA (Drugs)·D-0637-2020·2019-12-18
AuroMedics Recalls Mirtazapine Tablets Due to Labeling Error
AuroMedics Pharma LLC is recalling Mirtazapine 15 mg tablets that were incorrectly labeled as 7.5 mg. The error affects 500-count bottles distributed nationwide.
Product
MIRTAZAPINE — MIRTAZAPINE (MIRTAZAPINE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-0239-2020·2019-12-18
Cain Food Industries Recalls ASCORBO 150 Powder for Salmonella Risk
Cain Food Industries is recalling ASCORBO 150 Powder due to possible Salmonella contamination. The product was distributed in seven states.
Product
ASCORBO 150 POWDER packaged in 50 lb. Multi-wall paper bag with polyethylene liner
Category
Food
Distribution
7 states
SevereFDA (Food)·F-0244-2020·2019-12-18
Cain Food Industries Recalls OXIBAKE YF for Possible Salmonella Contamination
Cain Food Industries is recalling 1,000 pounds of OXIBAKE YF due to possible Salmonella contamination. The product was distributed in seven states.
Product
OXIBAKE YF packaged in 50 lb. Multi-wall paper bag with polyethylene liner
Category
Food
Distribution
7 states
SevereFDA (Drugs)·D-0576-2020·2019-12-18
Jubilant Cadista Recalls Amantadine Hydrochloride Tablets Due to Foreign Object
Jubilant Cadista Pharmaceuticals is recalling 1,824 bottles of Amantadine Hydrochloride Tablets because a foreign object was found in a single tablet.
Product
Amantadine Hydrochloride Tablets, 100 mg, 100-count bottle, Rx only, Manufactured by: Jubilant Generics Ltd., Roorkee-247661, India; Marketed by: Jubilant Cadista Pharmaceuticals Inc., Salisbury, MD 21801, USA; NDC 59746-699-01.
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·19T024000·2019-12-18
Cooper Tire Recalls Specific Tires Due to Sidewall Defect
Cooper Tire is recalling specific Evolution Tour, Mastercraft, Hercules, Starfire, and Stratus tires due to an improper sidewall component that may cause tire deflation and tread separation.
Product
TIRES:SIDEWALL recall
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Food)·F-0245-2020·2019-12-18
Cain Food Industries Recalls SLB-R Powder for Salmonella Contamination
Cain Food Industries is recalling 2,000 pounds of SLB-R Powder due to possible Salmonella contamination. The product was distributed in seven states.
Product
SLB-R POWDER packaged in 50 lb. Multi-wall paper bag with polyethylene liner
Category
Food
Distribution
7 states
SevereFDA (Food)·F-0241-2020·2019-12-18
Cain Food Industries Recalls BETA P-130 for Possible Salmonella Contamination
Cain Food Industries is recalling 2,200 pounds of BETA P-130 due to possible Salmonella contamination. The product was distributed in seven states.
Product
BETA P-130 packaged in 50 lb. Multi-wall paper bag with polyethylene liner
Category
Food
Distribution
7 states