State

New York product recalls

73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

41776–41800 of 86765

SevereFDA (Food)·F-0922-2019·2019-02-20
Oskri Organic Peanut Butter Recalled for Potential Listeria Contamination
Oskri Corp. is recalling Organic Peanut Spicy Cayenne Butter due to potential Listeria monocytogenes contamination. The recall was expanded to include all Oskri manufactured butters.
Product
Organic Peanut Spicy Cayenne Butter, packaged in 16 oz. Plastic jars UPC 66016-40111, pouches UPC 66016-40164. Oskri, 528 E. Tyranena Park Rd, Lake Mills, WI 53551.
Category
Food
Distribution
21 states
SevereFDA (Drugs)·D-0453-2019·2019-02-20
Promise Pharmacy Recalls Ipamorelin Injections Due to Sterility Concerns
Promise Pharmacy is recalling 416 vials of Ipamorelin 9 mg injection because the product lacks sterility assurance. The affected lots were distributed nationwide.
Product
Ipamorelin, 9 mg injection, Rx Only, Promise Pharmacy Compounding Specialists 31818 US Hwy 19N, Palm Harbor, FL 34684
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0470-2019·2019-02-20
Promise Pharmacy Recalls Myer's Cocktail Vials Due to Sterility Concerns
Promise Pharmacy is recalling 5 vials of Myer's Cocktail due to a lack of sterility assurance. The product was distributed nationwide.
Product
Myer's Cocktail, Pyridoxine/Dexpanthenol/Calcium Gluconate/Niacinamide/Vit B6/Vit B1/Leucine/Vit B5/Riboflavin/Ascorbic Acid/Hydroxycobalamin/Magnesium Chloride, 10ml vial, Rx Only, Promise Pharmacy Compounding Specialists 31818 US Hwy 19N, Palm Harbor, FL 34684
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0464-2019·2019-02-20
Promise Pharmacy Recalls IGF-1-LR3 Injections Due to Sterility Concerns
Promise Pharmacy, LLC is recalling 59 vials of IGF-1-LR3, 3 mg injection due to a lack of sterility assurance. The product was distributed nationwide in the USA.
Product
IGF-1-LR3, 3 mg injection, Rx Only, Promise Pharmacy Compounding Specialists 31818 US Hwy 19N, Palm Harbor, FL 34684
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0434-2019·2019-02-20
Promise Pharmacy Recalls Prednisolone and Gatifloxacin Ophthalmic Solution for Sterility Concerns
Promise Pharmacy is recalling compounded Prednisolone and Gatifloxacin ophthalmic solution due to a lack of sterility assurance.
Product
Prednisolone and Gatifloxacin and Ketorolac Ophthalmic Solution 1%/0.5%/0.5%, Combo Drops: 3 mL Rx Only, Compounded Prescription, Promise Pharmacy 31818 US Hwy 19N, Palm Harbor FL 34684
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0485-2019·2019-02-20
Dr. Reddy's Recalls Levetiracetam Injection Due to Labeling Error
Dr. Reddy's Laboratories is recalling Levetiracetam Injection bags because the primary label incorrectly identifies the product strength and sodium chloride concentration.
Product
LEVETIRACETAM — LEVETIRACETAM (LEVETIRACETAM INJECTION)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0433-2019·2019-02-20
Promise Pharmacy Recalls Prednisolone and Gatifloxacin Eye Drops for Sterility Concerns
Promise Pharmacy is recalling 55 bottles of compounded Prednisolone and Gatifloxacin Ophthalmic Solution due to a lack of sterility assurance.
Product
Prednisolone and Gatifloxacin Ophthalmic Solution 1%/0.5%, Combo Drops 3 mL, Rx Only, Compounded Prescription, Promise Pharmacy 31818 US Hwy 19N, Palm Harbor, FL 34684
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0495-2019·2019-02-20
Tris Pharma Recalls Superpotent Infants' Ibuprofen Suspension
Tris Pharma is recalling 35,280 bottles of Infants' Ibuprofen due to potential higher-than-labeled ibuprofen concentrations.
Product
Infants' Ibuprofen, Concentrated Ibuprofen Oral Suspension, USP, (NSAID), 50 mg per 1.25 mL, Dye Free, Non-staining Berry Flavor, 1 FL OZ (30 mL) bottle, Distributed by: CVS Pharmacy, Inc., One CVS Drive, Woonsocket, RI 02895, UPC 0 50428 39961 3, NDC 50428-1252-4.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0493-2019·2019-02-20
Tris Pharma Recalls Infants' Ibuprofen Due to Higher Concentration
Tris Pharma is recalling specific lots of Infants' Ibuprofen because the medication may contain a higher concentration of ibuprofen than labeled.
Product
Infants' Ibuprofen, Concentrated Ibuprofen Oral Suspension, USP, (NSAID), 50 mg per 1.25 mL, Dye Free, Non-staining Berry Flavor, 0.5 FL OZ (15 mL) bottle, Distributed by: CVS Pharmacy, Inc., One CVS Drive, Woonsocket, RI 02895, UPC 0 50428 39338 3, NDC 59779-925-23.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0472-2019·2019-02-20
Promise Pharmacy Recalls Folic Acid Injection Due to Sterility Concerns
Promise Pharmacy, LLC is recalling Folic Acid Injection, 10 mg/mL, 10mL vials due to a lack of sterility assurance. The affected lots were distributed nationwide.
Product
Folic Acid, Injection, 10 mg/mL, 10mL vial, Rx Only, Promise Pharmacy Compounding Specialists 31818 US Hwy 19N, Palm Harbor, FL 34684
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0824-2019·2019-02-20
Steris ATLAS Loading Car Recalled for Latch Failure Risk
Steris Corporation is recalling 129 ATLAS Loading Cars because the latch may fail to engage when empty, causing the unit to slide or fall.
Product
ATLAS Loading Car
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0882-2019·2019-02-20
RXBAR Chocolate Chip Bars Recalled for Undeclared Peanut Allergen
Chicago Bar Company LLC is voluntarily recalling RXBAR Chocolate Chip bars due to undeclared peanut. Consumers should stop eating the product.
Product
RXBAR: Chocolate Chip, 1.83oz bars, single bar,, 12-count carton, , 5-count carton,, 4-count carton
Category
Food
Distribution
43 states
HighFDA (Food)·F-0888-2019·2019-02-20
RXBAR Mixed Berry Bars Recalled for Undeclared Peanut Allergen
Chicago Bar Company is voluntarily recalling RXBAR Mixed Berry bars due to undeclared peanut. Consumers should stop eating the product and return it to the store.
Product
RXBAR: Mixed Berry, single bar, 12-count carton, UPC 57777 00470, 4-count carton
Category
Food
Distribution
43 states
HighFDA (Devices)·Z-0829-2019·2019-02-20
AtriCure Recalls COBRA FUSION 50 Ablation Systems Due to Thromboembolism Risk
AtriCure is recalling 1,288 COBRA FUSION 50 Ablation Systems because patients may face an elevated risk of thromboembolism during specific off-pump procedures.
Product
COBRA FUSION 50, Ablation System, Catalog # (REF) 700-002
Category
Medical Device
Distribution
37 states
HighFDA (Drugs)·D-0456-2019·2019-02-20
Promise Pharmacy Recalls IGF-1 LR3 Injections Due to Sterility Concerns
Promise Pharmacy is recalling 59 vials of IGF-1 LR3 injections because they lack sterility assurance. The affected products were distributed nationwide.
Product
IGF-1 LR3, 620 mcg injection, Rx Only, Promise Pharmacy Compounding Specialists 31818 US Hwy 19N, Palm Harbor, FL 34684
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0612-2019·2019-02-20
Philips CombiDiagnost R90 X-ray System Recalled for Radiation Dose Risk
Philips is recalling 146 CombiDiagnost R90 X-ray systems because a software defect may cause patients to receive increased radiation doses.
Product
Stationary Fluoroscopic X-ray System CombiDiagnost R90, Model 709030 Stationary Fluoroscopic X-ray System
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0892-2019·2019-02-20
RXBAR Pumpkin Spice Bars Recalled for Undeclared Peanut Allergen
Chicago Bar Company LLC is voluntarily recalling RXBAR Pumpkin Spice bars due to undeclared peanut allergen.
Product
RXBAR: Pumpkin Spice, single bar, 12-count carton, 4-count carton, 1.83 oz bars
Category
Food
Distribution
43 states
HighFDA (Food)·F-0891-2019·2019-02-20
RXBAR Recalls Kids Chocolate Chip Bars Due to Undeclared Peanut
RXBAR is voluntarily recalling Kids Chocolate Chip bars because they contain undeclared peanut, a major food allergen.
Product
KIDS Chocolate Chip, 1.16 oz. bars, single bar, 16-count carton, 5-count carton
Category
Food
Distribution
43 states
HighFDA (Food)·F-0895-2019·2019-02-20
RXBAR Recalls 12-Bar Variety Packs Due to Undeclared Peanut Allergen
Chicago Bar Company LLC is voluntarily recalling RXBAR 12-Bar Variety Packs because they contain undeclared peanut, a major food allergen.
Product
RXBAR: 12-Bar Variety Pack (Blueberry, Chocolate Sea Salt, Mixed Berry, Peanut Butter, Peanut Butter Chocolate), See Best By Date on individual bars as noted in other 12-bar pack, 1.83 oz. per bar
Category
Food
Distribution
43 states
HighNHTSA·19V112000·2019-02-20
Porsche Recalls One 2019 Cayenne Turbo for Shock Absorber Defect
Porsche is recalling one 2019 Cayenne Turbo because shock absorber forks may allow the shock absorbers to loosen, potentially impairing steering.
Product
PORSCHE — PORSCHE CAYENNE
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Food)·F-0889-2019·2019-02-20
RXBAR Recalls Apple Cinnamon Raisin Bars Due to Undeclared Peanut
Chicago Bar Company LLC is voluntarily recalling RXBAR KIDS Apple Cinnamon Raisin bars because they contain undeclared peanut.
Product
RXBAR: KIDS Apple Cinnamon Raisin, 1.16oz bars, single bar, 16-count carton, 5-count carton
Category
Food
Distribution
43 states
HighFDA (Food)·F-0880-2019·2019-02-20
RXBAR Apple Cinnamon Bars Recalled for Undeclared Peanut Allergen
Chicago Bar Company LLC is voluntarily recalling RXBAR Apple Cinnamon bars due to undeclared peanut. Consumers should check Best By dates and stop eating the product.
Product
RXBAR: Apple Cinnamon,1.83oz bars, single bar, 12-count carton,
Category
Food
Distribution
43 states
HighFDA (Devices)·Z-0831-2019·2019-02-20
AtriCure Recalls COBRA FUSION 150 Ablation System Due to Thromboembolism Risk
AtriCure is recalling 175 units of the COBRA FUSION 150 Ablation System because patients may face an elevated risk of thromboembolism during specific off-pump procedures.
Product
COBRA FUSION 150 Ablation System, Catalog # (REF) 700-001S
Category
Medical Device
Distribution
37 states
HighFDA (Food)·F-0890-2019·2019-02-20
RXBAR Recalls KIDS Berry Blast Bars Due to Undeclared Peanut Allergen
Chicago Bar Company LLC is voluntarily recalling KIDS Berry Blast bars because they contain undeclared peanut, a major food allergen.
Product
KIDS Berry Blast, 1.16 oz. bars, single bar, 16-count carton, 5-count carton
Category
Food
Distribution
43 states
HighFDA (Drugs)·D-0475-2019·2019-02-20
Promise Pharmacy Recalls Pyridoxine HCl Injection Due to Sterility Concerns
Promise Pharmacy, LLC is recalling 8 vials of Pyridoxine HCl Injection due to a lack of sterility assurance. The product was distributed nationwide in the USA.
Product
Pyridoxine HCl, 100 mg/mL Injection, 10ml vial, Rx Only, Promise Pharmacy Compounding Specialists 31818 US Hwy 19N, Palm Harbor, FL 34684
Category
Drug
Distribution
Distributed nationwide