State

New York product recalls

73,509 recalls have nationwide distribution and so reach New York. 12,945 additional recalls listed New York specifically in their distribution scope.

What the numbers show

Total: 12,945
Critical: 1,511
Severe: 3,698
Most recent: 2026-10-14

Of the 12,945 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 3,698 (29%) are Severe.

Which agencies issued them

These figures cover only the 12,945 recalls whose distribution notice names New York specifically. The 73,509 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

23226–23250 of 86454

ModerateFDA (Devices)·Z-1351-2022·2022-07-20
Philips LAS-100 Laser System may not operate due to detected hardware failure
Spectranetics' Philips LAS-100 Laser System (105 units) may fail to start if the device detects an inoperable hardware component during power-up, requiring manual error code clearing before operation.
Product
Philips Laser System, REF LAS-100, Intermittent Operation, Duty cycle dependent upon device in use 100 - 240 VAC, 50/60HZ, 16 AM
Category
Medical Device
Distribution
27 states
ModerateFDA (Devices)·Z-1375-2022·2022-07-20
Cathcart Hip Ball prosthesis recalled for missing surgical technique specification
DePuy Orthopaedics is recalling Modular Cathcart Hip Ball prostheses (sizes 41-60mm) because the Instructions for Use and Surgical Technique Guide did not document a +5mm offset specification. Updated guides now clarify this for hemi-hip arthroplasty procedures.
Product
MODULAR CATHCART FRACTURE HEAD HIP BALL, sizes 41mm to 60mm inclusive; metallic femoral head prosthesis, Product No. 136341000, 136342000, 136343000, 136344000, 136345000, 136346000, 136347000, 136348000, 136349000, 136350000, 136351000, 136352000, 136353000, 136354000…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1348-2022·2022-07-20
CoolCurve ZELTIQ vacuum applicators withdrawn due to increased Paradoxical Hyperplasia complaints
Zeltiq Aesthetics is removing 703 CoolCurve ZELTIQ vacuum applicators due to increased complaints of Paradoxical Hyperplasia reported between 2019 and 2021.
Product
CoolCurve ZELTIQ Vaccum Applicator REF BRZ-AP1-062-000
Category
Medical Device
Distribution
52 states
ModerateFDA (Devices)·Z-1384-2022·2022-07-20
Anti-FITC-AP CISH Kit Label Bears Incorrect Expiration Date
Agilent Technologies is recalling 63 Anti-FITC-AP CISH Accessory Kits due to incorrect expiration dates on substrate vial labels, which may result in the use of expired materials.
Product
Kit Label: Anti-FITC-AP CISH Accessory Kit (Dako Omnis), Box A REF K589911-2 Anti-FITC-AP CISH Accessory Kit (Dako Omnis), Box A REF K589911-21 Vial Labels: Mat. No K589911-21512
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-1418-2022·2022-07-20
AloePro Aloe Vera Dietary Supplement Recalled Nationwide for Product Spoilage
Premier Research Labs is recalling AloePro Aloe Vera dietary supplement nationwide due to product spoilage visible when opened. Consumers should discontinue use.
Product
AloePro Dietary Supplement Made With Organic ALOE VERA LIQUID 16 FL Oz. (475 mL) PREMIER RESEARCH LABS UPC Code: 80773500137 packaged in plastic HDPW bottles
Category
Food
Distribution
Distributed nationwide
SevereNHTSA·22E060000·2022-07-19
Cummins Recalls BP74E Battery Packs for Transit Bus Fire Risk
Cummins is recalling BP74E battery packs used in transit buses because internal coolant leaks can cause short circuits and increase fire risk.
Product
ELECTRICAL SYSTEM:PROPULSION SYSTEM:TRACTION BATTERY recall
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·22V510000·2022-07-19
Thomas Built Buses Recalling School Buses Due to Seat Frame Cracking
Daimler Trucks North America is recalling 2014-2023 Thomas Built Buses HDX and 2014-2022 EFX school buses because passenger seat frames may crack and rotate.
Product
THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER HDX, SAF-T-LINER EFX
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·22V509000·2022-07-19
2022 Kia Sorento and Telluride recalled for spare tire brake defect
Kia is recalling 2022 Sorento and Telluride vehicles with an incorrect spare tire that can impair the anti-lock braking and traction control systems. These defects increase the risk of a crash.
Product
KIA — KIA SORENTO, TELLURIDE
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·22E059000·2022-07-18
Besser Pro Recalls Trailer Axles Due to Weld Defects
Besser Pro is recalling 7000 lb Tubular Straight Axle assemblies for trailers because improper welds may cause cracking or separation, increasing crash risk.
Product
EQUIPMENT:RECREATIONAL VEHICLE/TRAILER recall
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·22V507000·2022-07-15
Arcimoto hybrid electric vehicles high voltage connector latch defect
Arcimoto is recalling certain 2019-2022 model year hybrid electric vehicles with a high voltage connector defect that may detach, causing sudden loss of power steering and drive power.
Product
ARCIMOTO — ARCIMOTO ROADSTER, FUV, DELIVERATOR, RAPID RESPONDER
Category
Vehicle
Distribution
Distributed nationwide
SevereUSDA FSIS·021-2022·2022-07-15
Ready Dough Pizza Recalls Pepperoni, Ham, and Bacon Products
Ready Dough Pizza Inc. is recalling approximately 8,018 pounds of pizza products produced without federal inspection and containing undeclared allergens.
Product
Ready Dough Pizza Inc. Recalls Pepperoni Pizza Products Produced Without Benefit of Inspection and also Due to Misbranding and Undeclared Allergens
Category
Food
Distribution
Distributed nationwide
SevereNHTSA·22E058000·2022-07-15
Engineered Controls Recalls Propane Service Valves for Leak Risk
Engineered Controls International is recalling specific propane service valves for recreational vehicles due to incorrect thread depth that may cause leaks.
Product
EQUIPMENT:RECREATIONAL VEHICLE/TRAILER:LPG SYSTEMS recall
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V508000·2022-07-15
Isuzu Recalls 2022 FTR and FVR Trucks Due to Engine Braking Defect
Isuzu is recalling 2022 FTR and FVR trucks because a software error disables engine braking, potentially increasing stopping distances and crash risk.
Product
ISUZU — ISUZU FTR, FVR
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·22V504000·2022-07-14
2022 Chrysler and Dodge vehicles recalled for tire pressure monitoring sensor failure
Chrysler and Dodge are recalling certain 2022 vehicles because TPMS sensors may fail prematurely, causing them to stop alerting drivers to low tire pressure. This can lead to tire failure and increase crash risk.
Product
CHRYSLER — CHRYSLER, DODGE 300, CHARGER, CHALLENGER
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·22758·2022-07-14
Westfield Outdoor Recalls Outfitter and Big Horn Tents for Smoke Inhalation Hazard
Westfield Outdoor is recalling approximately 5,050 Cabela's Outfitter and Big Horn camping tents because the stove jack ring can deteriorate under heat and create smoke inside the tent, posing a smoke inhalation risk.
Product
Outfitter and Big Horn tents
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·22E057000·2022-07-14
Chrysler Recalls Mopar Tire Pressure Sensors Due to Battery Failure
Chrysler is recalling Mopar Tire Air Pressure Sensors because the battery may fail prematurely. This can cause the system to stop working, increasing the risk of a crash.
Product
TIRES:PRESSURE MONITORING AND REGULATING SYSTEMS recall
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V505000·2022-07-14
Blue Bird Recalls School Buses Due to Electrical Grounding Defect
Blue Bird is recalling 2018-2022 school buses with Cummins electric drivetrains because an improperly grounded air compressor poses an electric shock risk.
Product
BLUE BIRD — BLUE BIRD VISION SCHOOL BUS, ALL AMERICAN SCHOOL BUS, ALL AMERICAN, VISION
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V506000·2022-07-14
Blue Bird Recalls One 2022 All American Transit Bus for Electrical Defect
Blue Bird is recalling one 2022 All American transit bus because an improperly grounded air compressor can cause electric shock.
Product
BLUE BIRD — BLUE BIRD ALL AMERICAN TRANSIT BUS
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·22185·2022-07-14
Sakar International Recalls Tony Hawk Silver Helmets Due to Head Injury Risk
Sakar International is recalling about 12,655 Tony Hawk Silver Metallic multi-purpose helmets sold at Walmart from March to June 2022. The helmets do not meet federal safety standards for positional stability and retention, and may fail to protect in a crash.
Product
Tony Hawk Silver Helmets
Category
Consumer Product
Distribution
Distributed nationwide
CriticalFDA (Food)·F-1402-2022·2022-07-13
Prairie City Bakery Peanut Butter Chocolate Chip Cakes Recalled for Salmonella
Prairie City Bakery is recalling Peanut Butter Chocolate Chip Ooey Gooey Butter Cakes due to Salmonella contamination from recalled Jif peanut butter ingredient. Products were distributed to gas stations and convenience stores nationwide.
Product
Prairie City Bakery Peanut Butter Chocolate Chip Ooey Gooey Butter Cake 2oz. individual UPC: 7-9788436718-2; 10 individual units per display unit; 6 display units per wholesale case.
Category
Food
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-1319-2022·2022-07-13
Palindrome HSI Chronic Catheter Recalled for Potential Hub Leaking
Covidien is recalling Palindrome HSI Chronic Catheters due to a potential leaking condition in the catheter hub that may cause unanticipated fluid return during dialysis. Approximately 13,526 units distributed worldwide are affected.
Product
Palindrome HSI Chronic Catheter, Sterile, Single Use, Rx Only. For acute and chronic hemodialysis, apheresis, and infusion.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1312-2022·2022-07-13
Palindrome Precision Chronic Dialysis Catheter Hub Leak Risk
Palindrome Precision Chronic Catheters used for dialysis may leak due to a flaw in the hub component, potentially allowing unintended fluid to escape during treatment.
Product
Palindrome Precision Chronic Catheter, Sterile, Single Use, Rx Only. For vascular access for acute and chronic hemodialysis, apheresis, and infusion.
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·22V503000·2022-07-13
2022 CAN-AM Ryker Motorcycles: Handlebar Stem Bolt Breakage Recall
CAN-AM is recalling 2022 Ryker motorcycles due to handlebar stem bolts that may break unexpectedly, causing sudden loss of steering control and crash risk.
Product
CAN-AM — CAN-AM RYKER
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Food)·F-1411-2022·2022-07-13
Built Bar Banana Cream Pie Puffs Protein Bars Recalled for Potential E. coli Contamination
Built Brands LLC is recalling approximately 4,196 individual Banana Cream Pie Puffs Protein Bars sold nationwide due to potential Escherichia coli contamination.
Product
Built Bar, Banana Cream Pie Puffs Protein Bar, 1.41 oz. (40 g) net wt., packaged in individual wrapper, Built Brands, LLC, 600 E Quality Dr., American Fork, UT 84003. SKU 30000318. Product sold as part of a paperboard 12-count mixed box. Each box contains 4 affected bars. UPC 8…
Category
Food
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1175-2022·2022-07-13
CVS Health Magnesium Citrate Laxative Recalled for Bacterial Contamination
CVS Health Magnesium Citrate SALINE LAXATIVE Oral Solution (1.745 g, Lemon Flavor, 10 FL OZ) is being recalled due to microbial contamination with Gluconacetobacter Liquefaciens. Approximately 98,958 bottles distributed nationwide are affected.
Product
CVS Health Magnesium Citrate SALINE LAXATIVE, Oral Solution, 1.745 g, Lemon Flavor, 10 FL OZ (296 mL), Distributed by: CVS Pharmacy, Inc., One CVS Drive, Woonsocket, RI 02895, UPC 0 50428 30594 2.
Category
Drug
Distribution
Distributed nationwide