State

New York product recalls

73,722 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 73,722 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

28701–28725 of 86677

HighFDA (Devices)·Z-1951-2021·2021-06-30
LEGION Knee Prosthesis Component Recalled for Manufacturing Surface Damage
Smith & Nephew is recalling 5 units of a knee prosthesis component due to surface damage from a manufacturing error. The affected lot was distributed in specific U.S. states.
Product
LEGION Posterior Stabilized OXINIUM Femoral Component, REF 71421216, Size 6, Left, Nonporous Femoral Component, A/P 65.5 MM, M/L 73 MM, For Cemented Use Only, ZR-2.5NB,Sterile. Knee prosthesis component.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1916-2021·2021-06-30
Transducer Cover Lacks FDA 510(k) Clearance for Surgical Use
Exact Medical Manufacturing is recalling 500 ultrasound transducer covers lacking FDA 510(k) clearance for body cavity use. The affected lot was distributed to Florida, Montana, New York, Ohio, Georgia, and Puerto Rico.
Product
Transducer Cover 18x147cm, Kit, VIP Film w/ Bands & EMM Gel- Ultrasonic Transducer Cover Item ID: E6360
Category
Medical Device
Distribution
6 states
HighFDA (Devices)·Z-1914-2021·2021-06-30
Ultrasonic Probe Covers Lack FDA Clearance for Body Use
Exact Medical Manufacturing recalls ultrasonic transducer probe covers marketed without required FDA 510(k) clearance for use in body openings. Approximately 129,600 units distributed to FL, MT, NY, OH, GA, and Puerto Rico.
Product
Probe Cover Elastic Poly 6" x 48"- Ultrasonic Transducer Cover Item ID: E5322N
Category
Medical Device
Distribution
6 states
HighFDA (Devices)·Z-1936-2021·2021-06-30
OneTouch Ultra Blue test strips recalled for temperature exposure damage
Cardinal Health is recalling 5,356 boxes of OneTouch Ultra Blue test strips after units were exposed to freezing temperatures during shipping, which may cause inaccurate glucose readings.
Product
ONETOUCH ULTRA BLUE TEST STRIPS 100 COUNT Item Number: 2990174
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1927-2021·2021-06-30
Cardiac assessment system may display test reports in wrong patient records
GE Healthcare's Case Cardiac Assessment System and CardioSoft diagnostic application may display one patient's cardiac test report in another patient's medical record under certain conditions. No patient injuries have been reported.
Product
Case Cardiac Assessment System for Exercise Testing and CardioSoft Diagnostic System Exercise Stress Testing ECG application
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0686-2021·2021-06-30
Clio Vanilla Greek Yogurt Mini Bars Recalled for Possible Metal Fragments
Clio LLC is recalling Clio Vanilla Greek Yogurt Mini Bars due to the possibility of metal fragments in the product. Consumers should not consume affected yogurt bars.
Product
Clio Vanilla Greek Yogurt Mini Bars wrapped in a Chocolate Coating 6.2oz pouch x 6 pouches per case, UPC: 854021008077
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1932-2021·2021-06-30
AeroChamber PLS Spacer Recalled Due to Temperature Exposure During Shipping
Cardinal Health is recalling AeroChamber PLS spacers exposed to freezing temperatures during shipping, which may cause inaccurate drug delivery results. Affected units shipped between February and March 2021 in Florida, Georgia, and South Carolina.
Product
AEROCHAMBER PLS W/MASK LRG BLU Item Number: 1496033
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1917-2021·2021-06-30
Ultrasonic Probe Cover Recalled for Missing FDA 510(k) Clearance
Exact Medical Manufacturing is recalling ultrasonic probe covers lacking required FDA 510(k) clearance for use in natural or surgical body openings. The 51,300 affected units were distributed across six U.S. states and Puerto Rico.
Product
Probe Cover, 6" x 96", PE, w 3 elastic bands- Ultrasonic Transducer Cover Item ID: E6443N
Category
Medical Device
Distribution
6 states
HighFDA (Food)·F-0693-2021·2021-06-30
Clio Peach Less Sugar Yogurt Bars recalled for possible metal fragments
Clio LLC is recalling Clio Peach Less Sugar Yogurt Bars due to the possible presence of metal fragments in the product. The 10-pack boxes with best buy dates between 2/7/2021 and 6/20/2021 were distributed nationwide.
Product
Clio Peach Less Sugar Yogurt Bars wrapped in a Chocolate Coating 50g x 10 Clio Retail 10-pack, UPC code: 854021008213
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0690-2021·2021-06-30
Clio Honey Greek Yogurt Bars Recalled for Possible Metal Fragments
Clio LLC is recalling Clio Honey Greek Yogurt Bars due to the possibility of metal fragments in the product. The recall affects 5,423 cases distributed nationwide with best-by dates between March 7, 2021 and July 11, 2021.
Product
Clio Honey Greek Yogurt Bars wrapped in a Chocolate Coating 50g x 10 Clio Retail 10-pack, UPC code: 861703000168
Category
Food
Distribution
Distributed nationwide
HighNHTSA·21V492000·2021-06-30
2021 Volkswagen Jetta Air Bag Control Module Welding Defect Recall
Volkswagen is recalling 2020-2021 Jetta vehicles because the air bag control module was welded in an incorrect position. This can cause air bags to deploy improperly during a crash or deploy unexpectedly, increasing injury risk.
Product
VOLKSWAGEN — VOLKSWAGEN JETTA
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Food)·F-0697-2021·2021-06-30
Clio Greek Yogurt Bars Recalled for Possible Metal Fragments
Clio LLC is recalling Clio Vanilla and Strawberry Club pack Greek Yogurt Bars nationwide due to the possibility of metal fragments in the product. Consumers should not eat the affected bars.
Product
Clio Vanilla / Strawberry Club pack Greek Yogurt Bars wrapped in a Chocolate Coating 50g x 12 , 16pc tray, 24g x 24 (12pc tray), 55g x 16 (8pc tray). UPC codes: 854021008121, 854021008138, and 854021008022
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1906-2021·2021-06-30
SARS-CoV-2 IgG II Calibrator Results Potentially Multiplied by 1000
Beckman Coulter's Access SARS-CoV-2 IgG II Calibrator may return test results inflated by up to 1000-fold due to software errors, potentially misrepresenting patient immune status.
Product
Access SARS-CoV-2 lgG II Calibrator, REF C69058, IVD, CE UDI: (01)15099590742751
Category
Medical Device
Distribution
31 states
HighFDA (Devices)·Z-1912-2021·2021-06-30
Ultrasound Transducer Probe Covers Recalled for Missing FDA Clearance
Exact Medical Manufacturing is recalling ultrasound transducer probe covers due to lack of FDA 510(k) clearance for use in natural or surgical body openings. The covers were distributed across six U.S. states and Puerto Rico.
Product
6" x 48" Elastic Poly Probe Cover, Tele Fold, sq. end,2 band - Ultrasonic Transducer Cover Item ID: A-AU-10- 058N
Category
Medical Device
Distribution
6 states
HighFDA (Food)·F-0692-2021·2021-06-30
Clio Mixed Berry Yogurt Bars Recalled for Possible Metal Fragments
Clio LLC is recalling Clio Mixed Berry Less Sugar Yogurt Bars due to possible metal fragments in the product. Consumers should not eat the affected bars and should contact the company or return them to the retailer.
Product
Clio Mixed Berry Less Sugar Yogurt Bars wrapped in a Chocolate Coating 10 Clio Retail 10-pack, UPC code: 854021008190
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1918-2021·2021-06-30
Hays Ultrasound Kit Recalled for Missing FDA Clearance
Exact Medical Manufacturing recalls 10,020 units of Hays Ultrasound Kit (H1000SE) due to lack of FDA 510(k) clearance for use in body openings. The recall affects units in FL, MT, NY, OH, GA, and Puerto Rico.
Product
Hays Ultrasound kit Item ID: H1000SE
Category
Medical Device
Distribution
6 states
HighFDA (Devices)·Z-1937-2021·2021-06-30
OneTouch Ultrasoft Lancets recalled due to temperature exposure during shipping
Cardinal Health is recalling 531 boxes of OneTouch Ultrasoft Lancets shipped February-March 2021 due to temperature exposure during shipment that may cause inaccurate test results.
Product
ONETOUCH ULTRASOFT LANCETS 100 COUNT Item Number: 3007788
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·21157·2021-06-30
Children's Nightgowns Recalled for Flammability Standard Violation
About 4,900 Booph children's nightgowns sold on Amazon from March through June 2021 are being recalled because they fail to meet federal flammability standards for sleepwear, posing a burn risk to children.
Product
Children's Nightgowns
Category
Consumer Product
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0638-2021·2021-06-30
Mephyton Phytonadione 5 mg Tablets Recall for Failed Impurity Specifications
Bausch Health Companies is recalling Mephyton (Phytonadione) 5 mg tablets nationwide because certain lots failed impurities and degradation specifications. Affected consumers should contact their healthcare provider.
Product
Mephyton (Phytonadione) 5 mg tablets, 100-count tablets, Rx Only, Manufactured for: Valeant Pharmaceuticals North America, LLC, Bridgewater, NJ, 08807, USA, NDC 0187-1704-05.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0702-2021·2021-06-30
Favorite Day Caramel Cashew Trail Mix Recalled for Plastic Contamination
John B. Sanfilippo & Son Inc. is recalling Favorite Day Caramel Cashew Trail Mix nationwide because the product may contain stringy pieces of flexible plastic.
Product
favorite day caramel cashew Trail Mix, Product Number 04312. Milk Chocolate caramel balls, cashews, M&M'S milk chocolate candies and Peanuts. Net Wt 14 oz. (396g), UPC 85239-15671
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1922-2021·2021-06-30
Ultrasonic Transducer Probe Covers Recalled Due to Missing FDA Clearance
Exact Medical Manufacturing recalled 36,000 ultrasonic transducer probe covers due to missing FDA 510k premarket notification clearance. The affected units were distributed to Florida, Montana, New York, Ohio, Georgia, and Puerto Rico.
Product
Probe Cover 6"x48"- Ultrasonic Transducer Cover Item ID: SH29
Category
Medical Device
Distribution
6 states
ModerateFDA (Devices)·Z-1945-2021·2021-06-30
Medical Action Industries Hemostats Recalled for Flaking Metal Defects
Medical Action Industries is recalling Mosquito Hemostats due to potential flaking metal and brown spots on the devices. The recall affects 23 boxes of surgical instruments distributed nationwide.
Product
Medical Action INDUSTRIES INC., Disposable Instrument Pack Mosquito Hemostat, REF 56220
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1907-2021·2021-06-30
Ultrasonic Probe Covers Recalled for Missing FDA Clearance
Exact Medical Manufacturing is recalling ultrasonic probe covers due to missing FDA 510(k) clearance for use in natural or surgical body openings. The recall affects 8,800 units distributed to Florida, Montana, New York, Ohio, Georgia, and Puerto Rico.
Product
Probe Cover 6" x 48" regular PE w/ 2 Elastic Bands-Ultrasonic Transducer Cover Bulk Non-sterile Item ID: A-AU-0776NA
Category
Medical Device
Distribution
6 states
ModerateFDA (Devices)·Z-1942-2021·2021-06-30
Blood Glucose Test Strips Recalled for Temperature Exposure During Shipping
Cardinal Health is recalling ACCU-CHEK SMARTVIEW 100 test strips distributed in Florida, Georgia, and South Carolina due to temperature excursions during shipping that may cause inaccurate glucose readings.
Product
ACCU-CHEK SMARTVIEW 100 TEST STRIPS Item Number: 4742862
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0636-2021·2021-06-30
Diflorasone Diacetate Ointment recalled for foreign particles
Teligent Pharma is recalling Diflorasone Diacetate Ointment USP 0.05% due to the presence of foreign particles found during routine stability testing. The recall affects 6,240 tubes distributed nationwide.
Product
Diflorasone Diacetate Ointment USP, 0.05%, packaged in a)15 g (NDC 52565-063-15) and b) 30 g (NDC 52565-063-30) tubes, Rx only, Manufactured by: Teligent Pharma, Inc, Buena, NJ 08310.
Category
Drug
Distribution
Distributed nationwide