State

New York product recalls

72,982 recalls have nationwide distribution and so reach New York. 12,905 additional recalls listed New York specifically in their distribution scope.

What the numbers show

Total: 12,905
Critical: 1,501
Severe: 3,135
Most recent: 2026-09-16

Of the 12,905 recalls naming New York we have scored against our rubric, 1,501 (12%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 3,135 (24%) are Severe.

Which agencies issued them

These figures cover only the 12,905 recalls whose distribution notice names New York specifically. The 72,982 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

6426–6450 of 85887

HighFDA (Food)·H-0297-2025·2025-07-23
YoCrunch vanilla yogurt with Twix pieces may contain plastic pieces
YoCrunch Low Fat Yogurt with Toppers, Vanilla with Twix bar pieces, is being recalled because of foreign material in the form of plastic pieces.
Product
YoCrunch Low Fat Yogurt with Toppers, Vanilla with Twix bar pieces, Packaged in the following size containers: 1. Single Serve Cup, 6 oz. (170g) UPC 46675-00113 2. Multipack containing 4-4 oz. cups UPC 46675-01327 Keep Refrigerated. Distributed by Danone US, LLC, White Plai
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2120-2025·2025-07-23
VITROS Performance Verifier I lots can cause quality control drift
VITROS Chemistry Products Performance Verifier I is being recalled because quality control drift can occur with certain cholinesterase slide lots, which could produce erroneous patient results.
Product
Brand Name: VITROS Chemistry Products Product Name: VITROS Chemistry Products Performance Verifier I Model/Catalog Number: 806 7324 Software Version: Not Applicable Product Description: VITROS Chemistry Products Performance Verifier is an assayed control used to monitor perfo
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0534-2025·2025-07-23
Rizatriptan 10 mg tablets exceed the acceptable intake limit for nitrosamine
Rizatriptan Benzoate Tablets USP 10 mg are being recalled after detection of N-nitroso-dimethyl-rizatriptan above the FDA recommended acceptable intake limit.
Product
RIZATRIPTAN BENZOATE — RIZATRIPTAN BENZOATE (RIZATRIPTAN BENZOATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0519-2025·2025-07-23
Levothyroxine sodium 25 microgram bottles of 1000 assayed below specification
Levothyroxine Sodium Tablets, USP 25 mcg in 1000-count bottles from Accord Healthcare are being recalled because the product is subpotent. 2,352 bottles are affected.
Product
LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0525-2025·2025-07-23
Omeprazole capsule bottle contained a foreign divalproex sodium tablet
Omeprazole Delayed-release Capsules USP 20 mg are being recalled because a foreign Divalproex Sodium Extended-Release 250 mg tablet was found in a bottle. 1,476 bottles affected.
Product
OMEPRAZOLE — OMEPRAZOLE (OMEPRAZOLE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2116-2025·2025-07-23
SwabCap disinfecting caps may have an incomplete seal allowing alcohol evaporation
SwabCap Disinfecting Caps for needlefree connectors are being recalled because an incomplete seal may let isopropyl alcohol evaporate, which may result in inadequate disinfection. 1,445,600 units affected.
Product
SwabCap Disinfecting Cap for Needlefree Connectors: SwabSleeve, REF: SCXT3-5-2000; SwabCap, 200-ct. Box, REF: SCXT3-2000
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2119-2025·2025-07-23
NIO+ intraosseous device stabilizer may not release properly after insertion
The NIO Intraosseous Device Adult is being recalled because a manufacturing error means the built-in stabilizer may not be released properly after deployment and insertion. 516 US units affected.
Product
Brand Name: NIO+ Product Name: NIO Intraosseous Device Adult Model/Catalog Number: 105000908 Software Version: N/A Product Description: NIO devices are a spring-based, automatic intraosseous access device supplied Sterile and single use. Indicated for Intraosseous access to t
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0287-2025·2025-07-23
Crumbled cookie bars recalled over potential Listeria monocytogenes contamination
Crumbled Cookie Bar frozen stick novelties are being recalled because of potential Listeria monocytogenes contamination. The action covers 110,292 cases across all affected products.
Product
Crumbled Cookie Bar (85200), stick novelties 3 FL. Oz (89mL)., Individually packaged in a plastic bag. Master case that consists of 4 packers with 24 units in each packer, total 96 units in a master case. Keep Frozen.
Category
Food
Distribution
23 states
HighFDA (Devices)·Z-2121-2025·2025-07-23
VITROS Performance Verifier II lots can cause quality control drift
VITROS Chemistry Products Performance Verifier II is being recalled because quality control drift can occur with certain cholinesterase slide lots, which could produce erroneous patient results.
Product
Brand Name: VITROS Chemistry Products Product Name: VITROS Chemistry Products Performance Verifier II Model/Catalog Number: 8231474 Software Version: N/A Product Description: VITROS Chemistry Products Performance Verifier is an assayed control used to monitor performance on V
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2123-2025·2025-07-23
VITROS CHE slides sold in Japan can cause quality control drift
VITROS Chemistry Products CHE Slides supplied in Japan are being recalled because quality control drift can occur with certain Performance Verifier lots, which could produce erroneous patient results.
Product
VITROS Chemistry Products CHE Slides (Japan); Catalog Numbers: (1) 684 4074 (90 slides), (2) 684 4138 (300 slides);
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0288-2025·2025-07-23
Orange Cream bars recalled over potential Listeria monocytogenes contamination
Orange Cream Bar frozen stick novelties are being recalled because of potential Listeria monocytogenes contamination. The action covers 110,292 cases across all affected products.
Product
Orange Cream Bar (86010), stick novelties 2.5 FL. Oz (74mL)., Individually packaged in a plastic bag. Master case that consists of 4 packers with 24 units in each packer, total 96 units in a master case. Keep Frozen.
Category
Food
Distribution
23 states
HighFDA (Food)·H-0303-2025·2025-07-23
YoCrunch Snickers and Twix yogurt packages may contain plastic pieces
YoCrunch Lowfat Yogurt with Toppers two-product packages containing vanilla yogurt with Snickers and Twix pieces are being recalled because of foreign material in the form of plastic pieces.
Product
YoCrunch Lowfat Yogurt with Toppers. Two-product package. Contains 8-6oz (170g) cups of Vanilla Yogurt with Snickers pieces (cup UPC 46675-00112), and 8-6oz (170g) cups of Vanilla Yogurt with Twix bar pieces (cup UPC 46675-00113). Two-Pack UPC 46675-02614. Keep Refrigerat
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·H-0285-2025·2025-07-23
Strawberry Shortcake bars recalled over potential Listeria monocytogenes contamination
Strawberry Shortcake Bar frozen stick novelties are being recalled because of potential Listeria monocytogenes contamination. The action covers 110,292 cases across all affected products.
Product
Strawberry Shortcake Bar (85050), stick novelties 3 FL. Oz (89mL)., Individually packaged in a plastic bag. Master case that consists of 4 packers with 24 units in each packer, total 96 units in a master case. Keep Frozen.
Category
Food
Distribution
23 states
HighFDA (Food)·H-0296-2025·2025-07-23
YoCrunch vanilla yogurt with Snickers pieces may contain plastic pieces
YoCrunch Low Fat Yogurt with Toppers, Vanilla with Snickers pieces, is being recalled because of foreign material in the form of plastic pieces.
Product
YoCrunch Low Fat Yogurt with Toppers, Vanilla with Snickers pieces, Packaged in the following size containers: 1. Single Serve Cup, 6 oz. (170g) UPC 46675-00112 2. Multipack containing 4-4 oz. cups UPC 46675-01326 Keep Refrigerated. Distributed by Danone US, LLC, White Pla
Category
Food
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0523-2025·2025-07-23
Levothyroxine sodium 150 microgram tablets assayed below the approved specification
Levothyroxine Sodium Tablets, USP 150 mcg from Accord Healthcare are being recalled because the product is subpotent, with an assay below the approved specification. 4,921 bottles affected.
Product
LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·25V482000·2025-07-23
Hyundai IONIQ 5 battery bus bar may be improperly tightened
Hyundai is recalling certain 2025 IONIQ 5 vehicles because the high voltage battery may contain an improperly tightened bus bar that can short circuit. Owners are told to park outside until repaired.
Product
HYUNDAI — HYUNDAI IONIQ 5
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Food)·H-0290-2025·2025-07-23
Cotton Candy Twirl bars recalled over potential Listeria monocytogenes contamination
Cotton Candy Twirl Bar frozen stick novelties are being recalled because of potential Listeria monocytogenes contamination. The action covers 110,292 cases across all affected products.
Product
Cotton Candy Twirl Bar (86260), stick novelties 2.5 FL. Oz (74mL)., Individually packaged in a plastic bag. Master case that consists of 4 packers with 24 units in each packer, total 96 units in a master case. Keep Frozen.
Category
Food
Distribution
23 states
HighFDA (Drugs)·D-0532-2025·2025-07-23
Lisinopril and hydrochlorothiazide bottle contained a foreign antiretroviral tablet
Lisinopril and Hydrochlorothiazide Tablets 20 mg/12.5 mg are being recalled after a complaint that a sealed bottle contained a foreign tablet identified as atazanavir and ritonavir. 58,968 bottles affected.
Product
LISINOPRIL AND HYDROCHLOROTHIAZIDE — LISINOPRIL AND HYDROCHLOROTHIAZIDE (LISINOPRIL AND HYDROCHLOROTHIAZIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·H-0302-2025·2025-07-23
YoCrunch strawberry two-product yogurt packages may contain plastic pieces
YoCrunch Lowfat Yogurt with Toppers two-product packages containing strawberry yogurt with M&Ms and with Oreo pieces are being recalled because of foreign material in the form of plastic pieces.
Product
YoCrunch Lowfat Yogurt with Toppers. Two-product package. Contains 8-6oz (170g) cups of Strawberry Yogurt with milk chocolate M&Ms pieces (cup UPC 46675-00084), and 8-6oz (170g) cups of Strawberry Yogurt with Oreo pieces (cup UPC46675-00083). Two-Pack UPC 46675-02613. Kee
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2113-2025·2025-07-23
BLS PURE laser projectors shipped without a working remote interlock connector
BLS laser light show projectors, models PURE 5000 and PURE 10000, are being recalled because the remote interlock connector required by federal regulation was not installed or was not wired. 3 units affected.
Product
Laser light show projectors manufactured by BLS, Model PURE 5000/10000.
Category
Other
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2112-2025·2025-07-23
BLS laser show projectors shipped without a working remote interlock connector
BLS laser light show projectors, models CLUB 1000, 2000 and 4000, are being recalled because the remote interlock connector required by federal regulation was not installed or was not wired. 12 units affected.
Product
Laser light show projectors manufactured by BLS, Model CLUB 1000/2000/4000.
Category
Other
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0520-2025·2025-07-23
Levothyroxine sodium 50 microgram tablets assayed below the approved specification
Levothyroxine Sodium Tablets, USP 50 mcg from Accord Healthcare are being recalled because the product is subpotent, with an assay below the approved specification. 54,227 bottles affected.
Product
LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2122-2025·2025-07-23
VITROS CHE slides can cause quality control drift with performance verifiers
VITROS Chemistry Products CHE Slides are being recalled because quality control drift can occur with certain Performance Verifier lots, which could produce erroneous patient results.
Product
VITROS Chemistry Products CHE Slides; Catalog Numbers: (1) 191 4605 (300 slides), (2) 800 4707 (90 slides);
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2126-2025·2025-07-23
EMPOWR 3D knee tibial inserts were packaged with the wrong implant
EMPOWR 3D Knee Tibial Insert E-PLUS units are being recalled because of a packaging discrepancy in which incorrect tibial inserts were packaged. 20 units are affected.
Product
Brand Name: EMPOWR 3D KNEE TIBIAL INSERT - E-PLUS Product Name: EMPOWR 3D KNEETM INS, 11L 12MM, VE Model/Catalog Number: 341-12-711 Software Version: NA Product Description: Enovis" knee devices are intended for treatment of patients who are candidates for knee arthroplasty p
Category
Medical Device
Distribution
18 states
HighFDA (Food)·H-0284-2025·2025-07-23
Chocolate crunch cake bars recalled over potential Listeria monocytogenes contamination
Chocolate Crunch Cake Bar frozen stick novelties are being recalled because of potential Listeria monocytogenes contamination. The action covers 110,292 cases across all affected products.
Product
Chocolate Crunch Cake Bar (85000), stick novelties 3 FL. Oz (89mL)., Individually packaged in a plastic bag. Master case that consists of 4 packers with 24 units in each packer, total 96 units in a master case. Keep Frozen.
Category
Food
Distribution
23 states