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.

35251–35275 of 86696

SevereFDA (Food)·F-0635-2020·2020-02-12
Pizza Hut Garlic Dipping Sauce Recalled for Metal Fragments
Golden State Foods is recalling Pizza Hut Garlic Dipping Sauce due to metal fragments in a starch ingredient.
Product
Pizza Hut Garlic Dipping Sauce; 144 1.50 oz. cups Net Weight: 13.5 lbs. /6.12 kg Supplier ID: 0005320-01 GSF Product # 01918; Customer Product #: 0072917 Packed exclusively for use by Pizza Hut and its franchisees and licensees. Pizza hut, Plano, TX
Category
Food
Distribution
19 states
SevereFDA (Devices)·Z-1011-2020·2020-02-12
Cardinal Health Recalls Surgical Gowns Due to Unknown Contamination Levels
Cardinal Health is recalling AAMI 3 Royalsilk Surgical Gowns because they contain unknown levels of bioburden, microbiological flora, and particulate contamination.
Product
AAMI 3 ROYALSILK SURGGOWN BNS L, Gown. Item Code 9518NC
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1040-2020·2020-02-12
Cardinal Health Recalls Surgical Gowns Due to Unknown Contamination
Cardinal Health is recalling AAMI 3 surgical gowns because they contain unknown levels of bioburden, microbiological flora, and particulate contamination.
Product
AAMI 3 FABREINF SURG GOWN LARGE, Item Code 9511
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1003-2020·2020-02-12
Cardinal Health Recalls Surgical Gowns Due to Unknown Contamination
Cardinal Health is recalling AAMI 3 non-reinforced surgical gowns because they contain unknown levels of bioburden, microbiological flora, and particulate contamination.
Product
AAMI 3 NON-REINF SURG GOWN 2XL BNS, Item Code 9575NB
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1028-2020·2020-02-12
Cardinal Health Recalls Surgical Gowns Due to Unknown Contamination
Cardinal Health is recalling AAMI 3 Non-Reinf Surgical Gowns because they contain unknown levels of bioburden, microbiological flora, and particulate contamination.
Product
AAMI 3 NON-REINF SURGICAL GOWN XXL, Item Code 9575
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0916-2020·2020-02-12
King Vision Video Adapter Recalled for Reversed Image Display
King Systems Corp. is recalling King Vision Video Adapters because the display shows a reversed image, causing left and right actions to be inverted.
Product
King Vision Video Adapter Size 1/2. Laryngoscope used to examine and visualize a patients upper airway and aid in the placement of a tracheal tube. Model Number: KVLVA12
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1025-2020·2020-02-12
Cardinal Health Recalls Surgical Gowns Due to Unknown Contamination Levels
Cardinal Health is recalling AAMI 3 fabric-reinforced surgical gowns because they contain unknown levels of bioburden, microbiological flora, and particulate contamination.
Product
AAMI 3 FABRIC REINF SURG GOWN XL, Item Code 9541
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1020-2020·2020-02-12
Cardinal Health Recalls Surgical Gowns Due to Unknown Contamination Levels
Cardinal Health is recalling specific surgical gowns because they contain unknown levels of bioburden, microbiological flora, and particulate contamination.
Product
AAMI 3 NONRNF SURG GWN 2XL XLNG BNS, Item Code 9575ELNA
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1009-2020·2020-02-12
Cardinal Health recalls surgical gowns due to unknown contamination levels
Cardinal Health is recalling AAMI 3 Royalsilk surgical gowns because they contain unknown levels of bioburden, microbiological flora, and particulate contamination.
Product
AAMI 3 ROYALSILK SCRBNURGOWN BNS L, Gown. Item Code 90280NC
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1097-2020·2020-02-12
Stryker SafeAir Telescopic Smoke Evacuation Pencil Recalled for Burn Risk
Stryker is recalling SafeAir Telescopic Smoke Evacuation Pencils because hairline fractures in a component could allow electrical current to arc, potentially causing burns to patients or users.
Product
SafeAir Telescopic Smoke Evacuation Pencil, Product No. 0703 046 004. The product is a Bovie pencil that is 75 inches long compressed, with a telescoping shaft. UDI GTIN 37613327466332
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-0633-2020·2020-02-12
Ducktrap River of Maine Herring in Wine Sauce Recalled for Undeclared Milk
Ducktrap River of Maine LLC is recalling 12-ounce cans of Herring Center Cuts in Wine Sauce because the product contains undeclared milk.
Product
Ducktrap River of Maine Herring Center Cuts in Wine Sauce, 12 oz.
Category
Food
Distribution
14 states
SevereFDA (Devices)·Z-1035-2020·2020-02-12
Cardinal Health Recalls Surgical Gowns Due to Unknown Contamination
Cardinal Health is recalling specific lots of AAMI 3 surgical gowns because they contain unknown levels of bioburden, microbiological flora, and particulate contamination.
Product
AAMI 3 FABRNF SURG GWN XL 2 TOWELS, Gown. Item Code ASG9541
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0991-2020·2020-02-12
Cardinal Health Genius 3 Tympanic Thermometer Recalled for Accuracy Drift
Cardinal Health is recalling Genius 3 tympanic thermometers because readings may drift upward over time, potentially exceeding the stated accuracy range.
Product
Genius 3 Tympanic Thermometer- electric thermometer Item Code: 303013
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0963-2020·2020-02-12
Cook Inc. Recalls Roadrunner Hydrophilic PC Wire Guides Due to Loading Error
Cook Inc. is recalling Roadrunner Hydrophilic PC Wire Guides because they may be incorrectly loaded, causing the stiff tip to be introduced into patients instead of the flexible tip.
Product
Roadrunner Hydrophilic PC Wire Guide, Guidewire, Global Product Number G18629, G17866
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0933-2020·2020-02-12
Datascope Recalls Reinforced Introducer Sets Due to Sterility Concerns
Datascope is recalling specific lots of Reinforced Introducer Sets because breached pouches may have compromised sterility.
Product
Reinforced Introducer Sets Maquet 7.5 Fr., Part Number: 068400040305. It is an accessory to be used for percutaneous insertion of MAQUET IntraAortic Balloon Catheters.
Category
Medical Device
Distribution
36 states
HighFDA (Drugs)·D-0828-2020·2020-02-12
Ascend Recalls Olmesartan Medoxomil Tablets Due to cGMP Deviations
Ascend Laboratories is recalling 192 bottles of Olmesartan Medoxomil 20 mg tablets because they were released in error with an alternate API source before approval.
Product
OLMESARTAN MEDOXOMIL — OLMESARTAN MEDOXOMIL (OLMESARTAN MEDOXOMIL)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0936-2020·2020-02-12
B. Braun Recalls Y-Type Blood Sets Due to Leakage Risk
B. Braun Medical is recalling 1,050 Y-Type Blood Sets because they may leak at the joint between the blood filters and tubing.
Product
Y-Type Blood Set, Catalog Number 490293
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0966-2020·2020-02-12
Cook Inc. Recalls Angled Tip Ureteral Catheter Sets Due to Loading Error
Cook Inc. is recalling 13,388 Angled Tip Ureteral Catheter Sets because the wire guide may load incorrectly, causing the stiff tip to enter the patient instead of the flexible tip.
Product
Angled Tip Ureteral Catheter Set with Bentson PTFE Wire Guide, Ureteral Catheter, Global Product No. G19108 G14587 G15302 G14326
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0973-2020·2020-02-12
Cook Inc. Recalls C-Flex Double Pigtail Ureteral Stent Sets
Cook Inc. is recalling C-Flex Double Pigtail Ureteral Stent Sets because the wire guide may be incorrectly loaded, causing the stiff tip to be introduced into the patient instead of the flexible tip.
Product
C-Flex Double Pigtail Ureteral Stent Set, Global Product No. G14364 G14365 G14367
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1091-2020·2020-02-12
Centurion ENT Snuffer Kit Recalled for Incomplete Sterile Package Seals
Centurion Medical Products is recalling 146 units of ENT Snuffer Kits due to incomplete seals that may compromise sterility.
Product
Centurion- ENT SNUF3 SNUFFER KIT Y
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1067-2020·2020-02-12
Centurion Medical Products Recalls Sterile Pathology Containers Due to Seal Defects
Centurion Medical Products Corporation is recalling specific sterile pathology containers and kits because incomplete seals may compromise sterility. The products were distributed nationwide and in Ghana.
Product
Centurion- Pathology Container 1150ST STERILE GRADUATED CONTAINER, 32 OZ. 17070 AI OR CARDIAC STERILE KIT 3703ST STERILE PATHOLOGY CONTAINER 3706ST STERILE CONTAINER 165 OZ.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1088-2020·2020-02-12
Centurion OR2020 Basin Set Recalled for Incomplete Sterile Seals
Centurion Medical Products is recalling 188 units of the OR2020 Basin Set because incomplete seals may compromise sterility.
Product
Centurion- OR2020 BASIN SET
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1044-2020·2020-02-12
Centurion Neonatal PICC Trays Recalled for Incomplete Sterile Package Seals
Centurion Medical Products is recalling 957 Neonatal PICC Trays due to incomplete seals that may compromise sterility. The units were distributed nationwide and to Ghana.
Product
Centurion Neonatal PICC Tray: CVI2310 NEONATAL PICC INSERTION TRAY CVI2550 NEONATAL PICC INSERTION TRAY CVI2550 NEONATAL PICC INSERTION TRAY CVI2550 NEONATAL PICC INSERTION TRAY CVI2550 NEONATAL PICC INSERTION TRAY CVI3650 PEDS PICC INSERTION TRAY CVI3730 NEONATAL PICC…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1060-2020·2020-02-12
Centurion Blood Culture Collection Kit Recalled for Incomplete Seals
Centurion Medical Products Corporation is recalling blood culture collection kits due to incomplete seals that may compromise sterility.
Product
Centurion-BLOOD CULTURE COLLECTION KIT BP115 BLOOD CULTURE COLLECTION KIT
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1049-2020·2020-02-12
Centurion Medical Products Recalls Sterile Dressing Change Kits Due to Seal Defects
Centurion Medical Products is recalling various sterile dressing change kits and trays because incomplete seals may compromise sterility.
Product
Centurion- Dressing Change Kits DYNDC1182B PICC INSERTION TRAY DYNDC1251D CENTRAL LINE TRAY DYNDC1251D CENTRAL LINE TRAY DYNDC1586C CENTRAL LINE DRESSING NGE TRAY DYNDC1597A CVC DRESSING CHANGE TRAY DYNDC1796C TRAY, CENTRAL LINE DYNDC1796C TRAY, CENTRAL LINE DYNDC1800…
Category
Medical Device
Distribution
Distributed nationwide