State

New York product recalls

73,218 recalls have nationwide distribution and so reach New York. 12,939 additional recalls listed New York specifically in their distribution scope.

What the numbers show

Total: 12,939
Critical: 1,511
Severe: 3,148
Most recent: 2026-09-30

Of the 12,939 recalls naming New York we have scored against our rubric, 1,511 (12%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 3,148 (24%) are Severe.

Which agencies issued them

These figures cover only the 12,939 recalls whose distribution notice names New York specifically. The 73,218 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

15976–16000 of 86157

SevereFDA (Food)·F-1629-2023·2023-10-04
Sorbet Cake Products Recalled Due to Listeria Contamination Risk
Ice Cream House is recalling 8' and Mini Sorbet Cake products in strawberry/mango flavors due to potential Listeria monocytogenes contamination. Affected products were distributed in Ohio, New Jersey, and New York.
Product
8' Sorbet Cake Strawberry/Mango; parve; 1 PACK; UPC: 0-91404-15429-1 and Mini Sorbet Cake Strawberry / Mango; parve; 1 PACK; UPC: 0-91404-15132-0
Category
Food
Distribution
3 states
SevereFDA (Food)·F-1667-2023·2023-10-04
Mini Sorbet Recalled Due to Listeria Monocytogenes Contamination
Mini Sorbet products distributed in Ohio, New Jersey, and New York may be contaminated with Listeria monocytogenes. Consumers should not consume these products and should return them to the retailer.
Product
Mini Sorbet; parve; 9 PACK / SINGLE; UPC: 0-91404-15408-6
Category
Food
Distribution
3 states
SevereFDA (Food)·F-1649-2023·2023-10-04
10-Inch Cherry Sorbet Cake Recalled Due to Listeria
Ice Cream House recalls its 10-inch cherry sorbet cake (UPC 0-91404-15111-5) distributed in Ohio, New Jersey, and New York due to potential Listeria monocytogenes contamination.
Product
10'' Sorbet Cake cherry; parve; 1 PACK; UPC: 0-91404-15111-5
Category
Food
Distribution
3 states
SevereFDA (Food)·F-1630-2023·2023-10-04
Sorbet Layer Cake Recalled for Potential Listeria Contamination
ICE CREAM HOUSE recalled a 10'' Sorbet 4 Layer Cake for potential Listeria monocytogenes contamination. Distribution was in Ohio, New Jersey, and New York.
Product
10'' Sorbet 4 Layer Cake; parve; 1 PACK; UPC: 0-91404-15111-5
Category
Food
Distribution
3 states
SevereFDA (Food)·F-1659-2023·2023-10-04
Mini Cone ice cream recalled for potential Listeria monocytogenes contamination
ICE CREAM HOUSE is recalling Mini Cone ice cream products due to potential Listeria monocytogenes contamination. Affected products were distributed in Ohio, New Jersey, and New York.
Product
Mini Cone; dairy / parve; 6 PACK / SINGLE; UPC: 0-91404-15220-4
Category
Food
Distribution
3 states
SevereFDA (Food)·F-1647-2023·2023-10-04
Sorbet Product Recalled for Listeria monocytogenes Contamination Risk
Check'ice board Sorbet Pre-Cut is being recalled due to potential Listeria monocytogenes contamination. The product was distributed in Ohio, New Jersey, and New York.
Product
Check'ice board Sorbet Pre-Cut 12 Slices Straw/Mango/Van; parve; 1 PACK / SINGLE; UPC: 0-91404-15144-3
Category
Food
Distribution
3 states
SevereFDA (Food)·F-1684-2023·2023-10-04
Mini Sorbet Dippers Recalled for Potential Listeria Contamination
ICE CREAM HOUSE is recalling Mini Sorbet Dippers because they may be contaminated with Listeria monocytogenes. The affected products were distributed in Ohio, New Jersey, and New York.
Product
Mini Sorbet Dippers; parve; 6 PACK / SINGLE; UPC: 0-91404-15303-4
Category
Food
Distribution
3 states
SevereFDA (Food)·F-1660-2023·2023-10-04
Mini Ice Cream Lollies Recalled for Potential Listeria Contamination
Ice Cream House is recalling Mini Ice Cream Lollies because they may be contaminated with Listeria monocytogenes. The recalled products were distributed in Ohio, New Jersey, and New York.
Product
Mini Ice Cream Lollies; dairy / parve; 12 PACK / SINGLE; UPC: 0-91404-15110-8
Category
Food
Distribution
3 states
SevereFDA (Food)·F-1669-2023·2023-10-04
Mini Chocolate Sorbet Tarts Recalled for Listeria Contamination
Ice Cream House is recalling Mini Chocolate Sorbet Tarts (UPC 0-91404-15411-6) due to potential Listeria monocytogenes contamination. Products were distributed in Ohio, New Jersey, and New York.
Product
Mini Chocolate Sorbet Tarts; parve; 12 PACK / SINGLE; UPC: 0-91404-15411-6
Category
Food
Distribution
3 states
HighNHTSA·23E075000·2023-10-04
Dorman Recalls Front Suspension Ball Joints Due to Steering Loss Risk
Dorman Products is recalling specific front suspension ball joints because the ball stud may separate, leading to loss of steering control and increased crash risk.
Product
SUSPENSION:FRONT:CONTROL ARM:LOWER BALL JOINT recall
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2644-2023·2023-10-04
B.Braun NORM-JECT Luer Lock Solo 10ml Syringe Sterility Recall
B.Braun NORM-JECT Luer Lock Solo 10ml sterile syringes are being recalled because the sterile blister packaging may be damaged, potentially compromising sterility. The recall affects 604,800 units distributed nationwide.
Product
B.Braun NORM-JECT Luer Lock Solo, 10 ml, Sterile-Intended to be used to deliver (inject) or withdraw an accurate metered dose of a fluid to/from the body. Distributed by: Air-Tite Products Co., Inc, 565 Central Drive, Virginia Beach, VA 23454. REF: NJ-4606728-02
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2643-2023·2023-10-04
B. Braun NORM-JECT Sterile Syringes Recalled Due to Packaging Damage
B. Braun NORM-JECT Luer Solo 10 ml sterile syringes are recalled because blister packaging may be damaged, potentially compromising sterility. Approximately 534,000 units are affected; lot numbers 22M28C8 and 23A09C8 are included.
Product
B. Braun NORM-JECT Luer Solo, 10 ml, Sterile-Intended to be used to deliver (inject) or withdraw an accurate metered dose of a fluid to/from the body. Distributed by: Air-Tite Products Co., Inc, 565 Central Drive, Virginia Beach, VA 23454. REF: NJ-4606108-02
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1657-2023·2023-10-04
Mini Cigars Recalled for Potential Listeria Monocytogenes Contamination
Mini Cigars from Ice Cream House are recalled due to potential Listeria monocytogenes contamination. The products were distributed in Ohio, New Jersey, and New York.
Product
Mini Cigars; dairy / parve; 10 PACK / SINGLE; UPC: 0-91404-15120-7
Category
Food
Distribution
3 states
HighFDA (Devices)·Z-2640-2023·2023-10-04
3M Attest Biological Indicators Cap May Melt During Sterilization
3M is recalling 77,280 Attest biological indicators due to caps that may melt, deform, or crack during steam sterilization cycles, potentially compromising process validation.
Product
3M Attest Super Rapid 5 Steam-Plus Steam Challenge Pack, REF 41482VF; designed to qualify and monitor dynamic-air removal steam sterilization processes
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1673-2023·2023-10-04
Triangle Up Ice Cream Recalled for Potential Listeria Contamination
Ice Cream House is recalling Triangle Up Strawberry Mango Vanilla ice cream sold in Ohio, New Jersey, and New York due to potential Listeria monocytogenes contamination. No illnesses have been reported.
Product
Triangle Up Strawberry Mango Vanilla; parve; 6 PACK / SINGLE; UPC: 0-91404-15308-9
Category
Food
Distribution
3 states
HighFDA (Devices)·Z-2633-2023·2023-10-04
exoplan 3.1 Dental Software Filtering Error Affects Surgical Guide Planning
Dental planning software exoplan 3.1 contains a filtering error that may display all surgical guide options instead of only supported ones, potentially causing patient injury.
Product
exoplan version 3.1 Rijeka Software -A medical software, intended to support the pre-operative planning of dental implants using the visualization of the implant placement within images of the patents anatomy.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2629-2023·2023-10-04
Aquilex Fluid Control System May Cause Fluid Overload During Hysteroscopy
The Aquilex Fluid Control System (Models AQL-100PBS, AQL-100P) display may freeze at maximum volume (30,000 ml) during long procedures, causing inaccurate fluid monitoring and potential fluid overload.
Product
Aquilex Fluid Control System-Intended to provide fluid distension of the uterus during diagnostic and operative hysteroscopies and to monitor the volume differential between the irrigation fluid flowing into and out of the uterus. Models AQL-100PBS and AQL-100P
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2628-2023·2023-10-04
Ambu aView 2 Advance Monitor Recalled Due to Battery Combustion Risk
Ambu Inc. is recalling the aView 2 Advance Monitor because multiple impacts can cause the device to short-circuit and potentially combust the lithium-ion battery, resulting in smoke and flames.
Product
Ambu aView 2 A Monitor-The Ambu aView 2 Advance is intended to display live imaging data from compatible Ambu visualization devices, portable endoscopy system. Catalog No: 405011000
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2645-2023·2023-10-04
Stryker Recalls Expired Cinchlock SS Knotless Anchor Inserter Units
Stryker Corporation is recalling 96 units of the expired Cinchlock SS Knotless Anchor Inserter (Part Number CAT02462, Lot 19175AE2) distributed nationwide. Expired surgical devices may not perform reliably during use.
Product
Cinchlock SS Knotless Anchor Inserter, Part Number CAT02462
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2634-2023·2023-10-04
Medical devices recalled due to potential rodent exposure and temperature excursion
Inmar Supply Chain Solutions recalled various medical devices nationwide due to potential rodent exposure and temperature excursions. Affected products include bandages, tampons, condoms, blood glucose monitors, adult diapers, COVID-19 test kits, and pregnancy tests.
Product
Various Medical Products stored on pallets, including but not limited to bandages, tampons, condoms, blood glucose monitors, adult diapers, COVID-19 test kits, and pregnancy tests.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2638-2023·2023-10-04
3M Attest Biological Indicators Recalled for Defective Caps
3M is recalling specific lots of Attest biological indicators used in steam sterilization monitoring. Certain lots have caps that may melt, deform, or crack at sterilization temperatures of 132°C and 135°C, potentially compromising sterilization process verification.
Product
3M Attest Super Rapid Readout Steam Challenge Pack, REF 1496V; designed to qualify and monitor dynamic-air removal steam sterilization processes
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2639-2023·2023-10-04
3M Attest Sterilization Indicator Caps May Melt or Crack
3M is recalling 172,464 units of Attest biological indicators used to validate steam sterilization because caps may melt, deform, or crack during sterilization at 132°C and 135°C.
Product
3M Attest Super Rapid 5 Steam-Plus Steam Challenge Pack, REF 41482V; designed to qualify and monitor dynamic-air removal steam sterilization processes
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2635-2023·2023-10-04
Ivenix Infusion System Software Startup Delays in Certain Flow Rate Ranges
Fresenius Kabi USA has recalled Ivenix Infusion System Large Volume Pump software versions 5.0.0 and 5.0.1 due to startup time delays that may exceed 6 minutes at flow rates between 50-200 ml/hr.
Product
Ivenix Infusion System (IIS), Large Volume Pump (LVP) Software: 5.0.0 and 5.0.1 Part Number: LVP-SW-0004. Indicated for use in a hospital and in outpatient care environments for the controlled administration of fluids through clinically accepted routes of administration.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·23V672000·2023-10-04
2023 Harley-Davidson FLTRXSE Motorcycles Recalled for Brake Line Defect
Harley-Davidson is recalling 2023 FLTRXSE and FLHXSE motorcycles due to improperly secured rear brake line clamps. The brake line may chafe against the exhaust pipe, causing fluid leaks that reduce braking ability.
Product
HARLEY-DAVIDSON — HARLEY-DAVIDSON FLTRXSE, FLHXSE
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2632-2023·2023-10-04
Palindrome Chronic Catheter Kit recalls devices with incorrect length labeling
Covidien LP is recalling Palindrome Chronic Catheter Kit devices where some catheters labeled as 23 cm implant length actually contain 28 cm devices. The mislabeling could affect proper catheter placement.
Product
Palindrome Chronic Catheter Kit Symmetrical Tip14.5 Fr/Ch(4.8mm)x23cm
Category
Medical Device
Distribution
Distributed nationwide