State

New York product recalls

73,737 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 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

31026–31050 of 86692

SevereFDA (Drugs)·D-0165-2021·2020-12-23
Cipla Recalls Azacitidine Injection Vials Due to Sterility Concerns
Cipla is recalling 2,151 vials of Azacitidine for Injection due to potential sterility issues caused by improper sealing.
Product
Azacitidine for Injection 100 mg/vial For Subcutaneous and Intravenous Use Only Single-Dose Vial Manufactured by Shilpa Medicare Limited Jadcherla -509301 INDIA Distributed by: Cipla USA, Inc. 10 Independence Blvd, Suite 300 Warren, NJ 07059 NDC 69097-805-40
Category
Drug
Distribution
Distributed nationwide
SevereCPSC·21058·2020-12-23
Urban Outfitters Recalls Taper Candle Holders Due to Fire Hazard
Urban Outfitters is recalling Swirled and Sofia Taper Candle Holders because they can catch fire if they contact a flame. Consumers should stop using them and return them for a refund.
Product
Swirled Taper and Sofia Taper Candle Holders
Category
Consumer Product
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0572-2021·2020-12-23
DePuy Synthes 10.5mm Reamer Head Recalled for Breakage and Tissue Damage
Synthes (USA) Products LLC is recalling DePuy Synthes 10.5mm Reamer Heads for RIA 2 due to breakage rates exceeding expectations, which can cause tissue and bone damage.
Product
DePuy Synthes 10.5MM REAMER HEAD FOR RIA 2 STERILE-Orthopedic manual surgical instrument Part Code: 03.404.017S
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0584-2021·2020-12-23
DePuy Synthes 16.5mm Reamer Head Recalled for Breakage and Tissue Damage
Synthes (USA) Products LLC is recalling DePuy Synthes 16.5mm reamer heads because breakage exceeds expected rates, causing tissue and bone damage.
Product
DePuy Synthes 16.5MM REAMER HEAD FOR RIA 2 STERILE-Orthopedic manual surgical instrument Part Code: 03.404.029S
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0581-2021·2020-12-23
DePuy Synthes 15.0mm Reamer Head Recalled for Breakage and Tissue Damage
Synthes (USA) Products LLC is recalling DePuy Synthes 15.0mm Reamer Heads for RIA 2 due to breakage rates exceeding expectations, which can cause tissue or bone damage.
Product
DePuy Synthes 15.0MM REAMER HEAD FOR RIA 2 STERILE -Orthopedic manual surgical instrument Part Code: 03.404.026S
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0576-2021·2020-12-23
DePuy Synthes 12.5mm Reamer Head Recalled for Breakage and Tissue Damage
Synthes (USA) Products LLC is recalling DePuy Synthes 12.5mm Reamer Heads for RIA 2 due to breakage exceeding expected rates, which can cause tissue and bone damage.
Product
DePuy Synthes 12.5MM REAMER HEAD FOR RIA 2 STERILE -Orthopedic manual surgical instrument Part Code: 03.404.021S
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·20E093000·2020-12-23
Autosales Recalls Summit Racing 3-Ton Jack Stands Due to Ratchet Bar Failure
Autosales is recalling Summit Racing 3-Ton Jack Stands because the ratchet bar may fail, allowing a vehicle to fall. Owners should stop using the stands and contact Autosales for a refund.
Product
EQUIPMENT:MECHANICAL:ACCESSORY SCISSOR/SCREW/BOTTLE JACK/LIFT:STAND recall
Category
Consumer Product
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0587-2021·2020-12-23
DePuy Synthes 18.0mm Reamer Head Recalled for Breakage and Tissue Damage
Synthes (USA) Products LLC is recalling DePuy Synthes 18.0mm Reamer Heads for RIA 2 due to breakage exceeding expected rates, which can cause tissue and bone damage.
Product
DePuy Synthes 18.0MM REAMER HEAD FOR RIA 2 STERILE-Orthopedic manual surgical instrument Part Code: 03.404.032S
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0622-2021·2020-12-23
Biomet M/H Modular Stem Recalled for Potential Sterile Seal Breach
Biomet, Inc. is recalling 7,428 units of the M/H Modular Stem (Item 13-104756) because a breach in the sterile seal could lead to loss of sterility.
Product
M/H MODULAR STEM, Item number 13-104756 - Product Usage: intended for use in limb salvage procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0619-2021·2020-12-23
Biomet Reverse Shoulder System Recalled for Potential Sterile Seal Breach
Biomet is recalling specific lots of the Comprehensive Reverse Shoulder System because a breach in the sterile seal could lead to loss of sterility.
Product
Comprehensive Reverse Shoulder System, Item numbers 115394, 115395, 115396, 115398, 180550, 180551, 180552, 180553, 180554, 180555, 180556, 180557, 180558, 180559, 180560, 180562 - Product Usage: indicated for use in patients whose shoulder joint has a grossly deficient…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0627-2021·2020-12-23
Biomet Ringloc Acetabular System Screws Recalled for Sterile Seal Breach
Biomet is recalling specific lots of Ringloc Acetabular System self-tapping bone screws because a breach in the sterile seal could lead to loss of sterility.
Product
RINGLOC ACETABULAR SYSTEM Self-tapping bone screws, Item numbers 103531, 103533, 103534, 103535 - Product Usage: Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented; Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented; Prosthesis, Hip, Semi-Constrained…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0630-2021·2020-12-23
Biomet Recalls Titanium IFS Devices Due to Potential Sterile Seal Breach
Biomet, Inc. is recalling 7,428 units of Titanium IFS devices (Item 909680) because a breach in the sterile seal could lead to loss of sterility.
Product
Titanium IFS, Item number 909680 - Product Usage: Bone to bone fixation.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0618-2021·2020-12-23
Biomet Cannulated Screw System Recalled for Potential Sterile Seal Breach
Biomet is recalling specific lots of cannulated screw systems because a breach in the sterile seal could lead to loss of sterility.
Product
6.5/8.0mm Cannulated Screw System, BCS Cannulated Screw System (3.0, 4.0/5.0, 6.5/8.0mm), Item numbers 110009929, 110009934, 110009935, 110009936, 110009993, 110009994, 110009996, 110009998, 110010000, 110010003, 110010029, 110010030, 110010032, 110010099 - Product Usage…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0625-2021·2020-12-23
Biomet Phoenix Interlocking Screws Recalled for Potential Sterile Seal Breach
Biomet is recalling specific lots of Phoenix interlocking screws because a breach in the sterile seal could lead to loss of sterility.
Product
PHOENIX, Interlocking screw for IM nail, Item numbers 14-405040, 14-405042, 14-405044, 14-405070 - Product Usage: Fracture fixation of small bones, small bone fragements and long bones.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0626-2021·2020-12-23
Biomet RapidFire Clip Recall Due to Potential Sterile Seal Breach
Biomet is recalling specific lots of RapidFire Clips used for craniofacial bone fixation because a breach in the sterile seal could lead to loss of sterility.
Product
RapidFire Clip, Item Number 95-0154 - Product Usage: Fixation of Craniofacial bone.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0631-2021·2020-12-23
Biomet RingLoc+ Drill Bits Recalled for Potential Sterile Seal Breach
Biomet is recalling specific lots of RingLoc+ Quick Connect Drill Bits because a breach in the sterile seal could lead to loss of sterility.
Product
RingLoc+ Quick Connect Drill Bit, Item numbers 31-323215, 31-323220, 31-323230, 31-323240 - Product Usage: Bit, Drill.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0616-2021·2020-12-23
Biomet Recalls Cannulated Screw Systems Due to Potential Sterile Seal Breach
Biomet is recalling specific lots of cannulated screw systems because a breach in the sterile seal could lead to loss of sterility.
Product
3.0mm Cannulated Screw System, BCS Cannulated Screw System (3.0, 4.0/5.0, 6.5/8.0mm), Item numbers 110009787 110009790, 110009794, 110009796, 110009798, 110009800 - Product Usage: Fracture fixationof small bones, small bone fragements and long bones.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0624-2021·2020-12-23
Biomet Oxford Fixed Lateral Knee Implants Recalled for Sterile Seal Breach
Biomet is recalling specific lots of Oxford Fixed Lateral knee implants because a breach in the sterile seal could lead to loss of sterility.
Product
Oxford Fixed Lateral, Item numbers 154330, 154370, 154373 154376 - Product Usage: indicated for use in the lateral compartment and intended to be implanted with bone cement.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0564-2021·2020-12-23
FDA Recalls Tempus LS Manual Defibrillators Due to Software Error
Remote Diagnostic Technologies is recalling 175 Tempus LS manual defibrillators because a software error may delay therapy by disrupting ECG calibration.
Product
Tempus LS - Manual Defibrillator, Model Number: 00-3020 Software Version: 1.3.4 - Product Usage: The device is intended to be used in the following environmental: - Primarily in pre-hospital care and transport applications (including ambulances, fixed and rotary wing aircraft).
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0590-2021·2020-12-23
Enterix Recalls InSure ONE Test Strips Due to Potential False Positives
Enterix, Inc. is recalling InSure ONE Test Strips because they may produce false positive results, potentially leading to unnecessary medical procedures.
Product
InSure ONE Test Strips (25 pack) vials-fecal immunochemical test (FIT) qualitatively detects human hemoglobin from blood in fecal samples Model 12045.01.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0589-2021·2020-12-23
RaySearch Recalls RayStation and RayPlan Software Due to Treatment Plan Errors
RaySearch is recalling RayStation and RayPlan software versions due to potential errors in treatment plan reports, including incorrect dose information and couch angles.
Product
RayStation 4, 4.5, 4.7, 4.9, 5, 6, 7, 8A, 8B, 9A, 9B, RayPlan 1, 2, 7, 8A, 8B, 9A, 9B, including all service packs. RayStation 10A and RayPlan 10A are also affected, but not the 10A service pack. (Model No. 4.0, 4.5, 4.7, 4.9, 5.0, 6.0, 6.1, 6.2, 6.3, 7.0, 8.0, 8.1, 9.0, 9.1…
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·21057·2020-12-23
GSK Recalls Five Excedrin Brands Due to Child-Resistant Packaging Defects
GSK Consumer Healthcare is recalling five Excedrin brands because some bottles have holes in the bottom, posing a risk of poisoning to children.
Product
Excedrin Migraine Caplets, Excedrin Migraine Geltabs, Excedrin Extra Strength Caplets, Excedrin PM Headache Caplets, and Excedrin Tension Headache Caplets
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0569-2021·2020-12-23
Ra Medical Systems Recalls DABRA Laser Due to Footswitch Defect
Ra Medical Systems is recalling 36 DABRA Laser devices because the footswitch may fail to protect against liquid ingress, potentially causing the laser to remain on.
Product
DABRA Laser (RA-308 Excimer Laser) Intended Use: For use in ablating a channel in occlusive peripheral vascular disease. Indications: For crossing chronic total occlusions in patients with symptomatic infrainguinal lower extremity vascular disease.
Category
Medical Device
Distribution
16 states
HighFDA (Devices)·Z-0623-2021·2020-12-23
Biomet OSS Polyethylene Tibial Bushing Recalled for Sterile Seal Breach
Biomet is recalling specific lots of OSS Polyethylene Tibial Bushings because a breach in the sterile seal could lead to loss of sterility.
Product
OSS Polyethylene Tibial Bushing, Item number 150476 - Product Usage: intended for use in limb salvage.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0613-2021·2020-12-23
Carl Zeiss Meditec VISULENS 550 Recalled for Electrical Shock Risk
Carl Zeiss Meditec is recalling VISULENS 550 refractive power measurement devices due to a defective communication board that may cause electrical shocks.
Product
Carl Zeiss Meditec Ag VISULENS 550 REF 2268-038 - Product Usage: is a device for measuring the refractive power of contact lenses and spectacle lenses and displaying measurement values for sphere, cylinder and prism.
Category
Medical Device
Distribution
Distributed nationwide