State

New York product recalls

73,817 recalls have nationwide distribution and so reach New York. 12,956 additional recalls listed New York specifically in their distribution scope.

What the numbers show

Total: 12,956
Critical: 1,508
Severe: 3,702
Most recent: 2026-11-04

Of the 12,956 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 3,702 (29%) are Severe.

Which agencies issued them

These figures cover only the 12,956 recalls whose distribution notice names New York specifically. The 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

47126–47150 of 86773

ModerateFDA (Drugs)·D-0386-2018·2018-02-21
Sage Products Recalls Oral Cleansing Systems Due to Cross-Contamination
Sage Products Inc. is recalling 25 cases of Oral Cleansing & Suctioning Systems because they were manufactured on equipment shared with non-pharmaceutical products.
Product
Oral Cleansing & Suctioning System with 0.12% Chlorhexidine Gluconate (CHG) Oral Rinse q2, Contains 1 Covered Yankauer and Y-Connector, 2 Untreated Suction Toothbrush packages, 2 Single dose bottles of 0.12% CHG Oral Rinse, 4 Packages Suction Oral Swab with sodium bicarbonate…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0632-2018·2018-02-21
Cook Inc. Recalls Central Venous Catheter Sets Due to Fit Issues
Cook Inc. is recalling 75 central venous catheter sets because they may not fit over a guide wire, potentially causing procedure delays.
Product
Central Venous Catheter Set Heparin Coated Triple Lumen Polyurethane, Catalog Identifiers: C-UTLM-501J-25-6.5-WCE-BH, C-UTLM-501J-BH Product Usage: The central venous catheter is designed for treatment of critically ill patients and is suggested for: 1. Continuous or…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0370-2018·2018-02-21
Sage Products Recalls Toothette Oral Care Suction Toothbrushes
Sage Products Inc. is recalling Toothette Oral Care Suction Toothbrushes due to cross-contamination with non-pharmaceutical products during manufacturing.
Product
Toothette Oral Care Suction Toothbrushes with Antiseptic Oral Rinse and Mouth Moisturizer, Contains 2 Suction Toothbrushes with sodium bicarbonate. 0.25 fl oz/7ml Antiseptic Oral Rinse, 0.07 oz/2g Mouth Moisturizer, Sage Products, Inc., 3909 Three Oaks Road, Cary, IL 60013.…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0410-2018·2018-02-21
Sage Products Recalls Chlorhexidine Skin and Oral Care Kits
Sage Products Inc. is recalling 150 cases of skin antisepsis and oral cleansing kits due to cross-contamination risks from shared manufacturing equipment.
Product
Skin antisepsis and oral cleansing. Contains Three 2-packs of 2% Chlorhexidine Gluconate Cloth Patient Preoperative Skin Preparation and One 7ml Burst Pouch of Corinz Antiseptic Cleansing and Moisturizing Oral Rinse, I Ultra-Soft Toothbrush, 1 Applicator Swab treated with Sodium…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0373-2018·2018-02-21
Sage Products Recalls Q CARE Oral Cleaning System Due to Cross-Contamination
Sage Products is recalling Q CARE q4 Oral Cleaning & Suctioning Systems because oral care solutions were manufactured on equipment shared with non-pharmaceutical products.
Product
Q CARE q4 Oral Cleaning & Suctioning System Contains 1 Covered Yankauer and Y-Connector, 2 Suction Toothbrush packages with Antiplaque solution, 4 Suction Oral Swab packages with Antiseptic Oral Rinse. Sage Products, Inc., 3909 Three Oaks Road, Cary, IL 60013. Product Code 6404…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0379-2018·2018-02-21
Sage Products Recalls Toothette Oral Care Suction Swabs Due to Cross-Contamination
Sage Products Inc. is recalling Toothette Oral Care Suction Swabs because they were manufactured on equipment shared with non-pharmaceutical products, posing a cross-contamination risk.
Product
Toothette Oral Care Suction Swabs with Perox-A-Mint solution and Mouth Moisturizer, Contains 2 Suctino Swabs with sodium bicarbonate, 0.25 fl oz/7ml Perox-A-Mint solution, 0.07 oz/2g Mouth Moisturizer. Sage Products, Inc., 3909 Three Oaks Road, Cary, IL 60013. Product Code 6513
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0401-2018·2018-02-21
Sage Q.Care Oral Cleansing System Recalled for Cross-Contamination Risk
Sage Products Inc. is recalling Q.Care Oral Cleansing & Suctioning Systems because oral care solutions were manufactured on equipment shared with non-pharmaceutical products.
Product
Q.Care Oral Cleansing & Suctioning System with 0.12% Chlorhexidine Gluconate (CHG) Oral Rinse q4. Contains 1 Covered Yankauer and Y-Connector, 2 Untreated Suction Toothbrush packages, 2 Single dose bottles of 0.12% CHG Oral Rinse, 4 Suction Oral Swab packages with Perox-A-Mint…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0350-2018·2018-02-21
Sage Products Recalls Toothette Oral Care Perox-A-Mint Solution
Sage Products is recalling Toothette Oral Care Perox-A-Mint Solution packets due to cross-contamination with non-pharmaceutical products during manufacturing.
Product
Toothette Oral Care Perox-A-Mint Solution, Oral Debriding Agent, 1.5 fl. oz./44 mL. packet. Sage Products, Inc., 3909 Three Oaks Road, Cary, IL 60013. Product Code 6065. UPC 6 18029 80018 3
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0414-2018·2018-02-21
FDA Recalls Bull Capsules Tainted with Sildenafil
BYL Solutions Inc. is recalling Bull Capsules marketed without an approved NDA/ANDA and found to be tainted with sildenafil.
Product
Bull Capsules, 1800 mg/grain, 30 count per tin, Hongkong Jiuyuejiu Biology Technology CO., LTD, BYL Solutions, Inc. dba Nutra Labs, Inc., Palmetto, FL
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0575-2018·2018-02-21
B. Braun Recalls Pain Management Trays with Foreign Matter
B. Braun Medical is recalling 460 Pain Management Trays containing 22GA SafetyGlide Needles due to the presence of loose polypropylene foreign matter.
Product
Pain Management Tray. Product Catalog Number: 560602. Local anesthesia of the skin prior to insertion of the regional anesthesia needle.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0623-2018·2018-02-21
Aesculap ELAN 4 Air System Recalled for Premarket Clearance Issues
Aesculap Implant Systems LLC is recalling 167 units of the ELAN 4 Air System because they were released to the market before receiving FDA 510(k) clearance.
Product
The ELAN 4 Air System is intended for high speed cutting, sawing and drilling of bone in fields of Spine, ENT, Neuro, and Maxillofacial Surgery.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0366-2018·2018-02-21
Sage Products Recalls Toothette Oral Care Perox-A-Mint Due to Cross-Contamination
Sage Products Inc. is recalling Toothette Oral Care Perox-A-Mint solution because it was manufactured on equipment shared with non-pharmaceutical products, posing a cross-contamination risk.
Product
Toothette Oral Care Perox-A- Mint solution, Oral Debriding Agent 8 fl oz/237 ml. Sage Products, Inc., 3909 Three Oaks Road, Cary, IL 60013. Product Code 6060 UPC (01)00618029800152
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0634-2018·2018-02-21
Cook Inc. Recalls Spectrum Central Venous Catheter Trays Due to Fit Issues
Cook Inc. is recalling 304 Spectrum Central Venous Catheter Trays because the catheters may not fit over the guide wire, potentially causing procedure delays.
Product
Spectrum Central Venous Catheter Tray Minocycline/Rifampin Antibiotic Impregnated, Catalog Identifiers: C-UTLMY-501J-ABRM-HC-FST and C-UTLMY-501J-ABRM-HC-IHI-FST Usage: The Spectrum Central Venous Catheter is used for the intravenous administration of nutrient fluids…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0796-2018·2018-02-21
Kingston Pharma Recalls Live Better Black Elderberry Syrup Due to Gas Development
Kingston Pharma LLC is recalling 13,536 bottles of Live Better Drug Free Black Elderberry Syrup because gas is developing in the sealed bottles.
Product
Live Better Drug Free Black Elderberry Syrup, 4 FL OZ (118 mL); DIETARY SUPPLEMENT, UPC 050428581186
Category
Food
Distribution
11 states
ModerateFDA (Drugs)·D-0384-2018·2018-02-21
Sage Products Recalls Toothette Oral Care Suction Toothbrush Due to Cross Contamination
Sage Products Inc. is recalling Toothette Oral Care Suction Toothbrush kits because oral care solutions were manufactured on equipment shared with non-pharmaceutical products.
Product
Toothette Oral Care Suction Toothbrush with Perox-A-Mint solution and Mouth Moisturizer. Contains 1 Suction Toothbrush with sodium Bicarbonate, 0.25 fl oz /7ml Perox-A-Mint solution, 0.07 oz/2g Mouth Moisturizer, 1 Applicator Swab, Sage Products, Inc., 3909 Three Oaks Road…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0399-2018·2018-02-21
Sage Q.Care Oral System Recalled for Cross-Contamination Risk
Sage Products is recalling Q.Care Oral Cleansing & Suctioning Systems because oral care solutions were manufactured on equipment shared with non-pharmaceutical products.
Product
Q.Care Oral Cleansing & Suctioning System with 0.12% Chlorhexidine Gluconate (CHG) Oral Rinse q2. Contains 1 Covered Yankauer and Y-Connector, 2 Untreated Suction Toothbrush packages, 2 Single dose bottles of 0.12% CHG Oral Rinse, 4 Suction Oral Swab packages with Perox-A-Mint…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0562-2018·2018-02-21
Philips Ingenuity TF PET/CT Software Recall for Reconstruction Failures
Philips is recalling 24 Ingenuity TF PET/CT systems due to a software defect that causes intermittent PET reconstruction failures, rendering acquired data unusable.
Product
Ingenuity TF PET/CT (model 882442) running software version 4.0.2 This device is a diagnostic imaging system that combines Positron Emission Tomography (PET) and X-ray Computed Tomography (CT) systems. The CT subsystem produces cross-sectional images of the body by computer…
Category
Medical Device
Distribution
5 states
ModerateFDA (Drugs)·D-0403-2018·2018-02-21
Sage Q.Care Oral Cleansing System Recalled for Cross-Contamination
Sage Products is recalling Q.Care Oral Cleansing & Suctioning Systems because oral care solutions were manufactured on equipment shared with non-pharmaceutical products.
Product
Q.Care Oral Cleansing & Suctioning System Suction Toothbrush Compatible with Chlorhexidine Gluconate (CHG) Oral Rinse q2. Contains 1 Covered Yankauer and Y-Connector, 2 Untreated, CHG Compatible Suction Toothbrush packages, 4 Suction Oral Swab packages with Perox-A-Mint…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0567-2018·2018-02-21
B. Braun Recalls Perifix Anesthesia Kits Due to Foreign Matter
B. Braun Medical is recalling Perifix Continuous Epidural Anesthesia Trays because they contain needles with loose polypropylene foreign matter.
Product
Perifix Continuous Epidural Anesthesia Tray. Product Catalog Numbers: 332075, 332266. Local anesthesia of the skin prior to insertion of the regional anesthesia needle.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0389-2018·2018-02-21
Sage Products Recalls Toothette Oral Care Systems Due to Cross-Contamination
Sage Products Inc. is recalling Toothette Oral Care Q Care & Suctioning Systems because oral care solutions were manufactured on equipment shared with non-pharmaceutical products.
Product
Toothette Oral Care Q Care & Suctioning System. Contains 1 Covered Yankauer, Suction Handle and Y-Connector, 2 Suction Toothbrush packages with Perox-A-Mint solution, 10 Suction Oral Swab packages with Perox-A-Mint solution, 4 Oropharyngeal Suction Catheter packages. Sage…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0421-2018·2018-02-21
BonaDur For Men Lidocaine Spray Recalled for Manufacturing Deviations
Webrx dba RxPalace.com is recalling BonaDur For Men lidocaine spray because it was not manufactured according to current good manufacturing practices.
Product
BonaDur For Men (lidocaine) spray, 10 mg per spray, Net Contents .25 fl. oz. (7.4 mL) spray bottles, Manufactured by WebRx Pharmacy Palace, Sarasota, FL 34232; NDC 70582-999-74
Category
Drug
Distribution
1 state
ModerateFDA (Devices)·Z-0574-2018·2018-02-21
B. Braun Recalls Epidural Anesthesia Kits Due to Foreign Matter
B. Braun Medical is recalling 120 units of Customer Epidural Anesthesia Trays because they contain needles with loose polypropylene foreign matter.
Product
Customer Epidural Anesthesia Tray. Product Catalog Number: 555234. Local anesthesia of the skin prior to insertion of the regional anesthesia needle.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0400-2018·2018-02-21
Sage Products Recalls Q.Care Oral Cleansing System Due to Cross-Contamination
Sage Products Inc. is recalling Q.Care Oral Cleansing & Suctioning Systems because oral care solutions were manufactured on equipment shared with non-pharmaceutical products.
Product
Q.Care Oral Cleansing & Suctioning System with 0.12% Chlorhexidine Gluconate (CHG) Oral Rinse q4. Contains 1 Covered Yankauer and Y-Connector, 2 Untreated Suction Toothbrush packages, 2 Single dose bottles of 0.12% CHG Oral Rinse, 4 Suction Oral Swab packages with Perox-A-Mint…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0354-2018·2018-02-21
Sage Products Recalls QCare RX Oral Cleansing System Due to Cross-Contamination
Sage Products is recalling 9,006 cases of QCare RX Oral Cleansing Systems because they were manufactured on equipment shared with non-pharmaceutical products.
Product
QCare RX Q2 Oral Cleansing & Suctioning System with 0.12% Chlorhexidine Gluconate (CHG) Oral Rinse Corinz. Contains 1 Covered Yankauer and Y-Connector, 2 Untreated Suction Toothbrush packages, 2 Single dose bottles of 0.12% CHG Oral Rinse, 10 Suction Oral Swab packages with…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0615-2018·2018-02-21
Pentax Video Cystoscopes Recalled for Lack of FDA Clearance
Pentax of America Inc is recalling 24 Video Cystoscopes because they lack required FDA premarket notification clearance.
Product
Video Cystoscope models ECY-1570 and ECY-1570K
Category
Medical Device
Distribution
9 states