Recalls in New York (page 23)

4155 recalls.

• UPC 29259700000 KITCHEN TRAY SUB SANDWICH SS This is recall (Albertsons Companies LLC)
  FoodClass IIReported June 10, 2026 · Contains statement does not declare Pistachio
• UPC 21243500000 KITCHEN SANDWICH ITALIAN SUPER SUB SS COLD This is A recall (Albertsons Companies LLC)
  FoodClass IIReported June 10, 2026 · Contains statement does not declare Pistachio
• UPC 21788400000 Ready Meals SANDWICH TUNA SALAD CROISSANT SS COLD T recall (Albertsons Companies LLC)
  FoodClass IIIReported June 10, 2026 · Contains statement does not declare TUNA
• UPC 21914600000 KITCHEN SANDWICH CROISSANT CHICKEN CASHEW SS This is recall (Albertsons Companies LLC)
  FoodClass IIIReported June 10, 2026 · Contains statement does not declare Cashew
• UPC 25678000000 CROISSANTS DUBAI CHOCOLATE 2CT This is Albertson's recall (Albertsons Companies LLC)
  FoodClass IIReported June 10, 2026 · Contains statement does not declare Pistachio
• UPC 25317100000 CROISSANTS ALMOND RASPBERRY FILLED 4CT This is Albe recall (Albertsons Companies LLC)
  FoodClass IIIReported June 10, 2026 · Contains statement does not declare Almond
• UPC 28586600000 CROISSANT ALMOND UPC 22102100000 CROISSANTS ALMOND 4 CT recall (Albertsons Companies LLC)
  FoodClass IIIReported June 10, 2026 · Contains statement does not declare Almond
• UPC 26911700000 COOKIES OATMEAL RAISIN 10CT This is Albertson's recall (Albertsons Companies LLC)
  FoodClass IIReported June 10, 2026 · Contains statement does not declare Almond
• UPC 22358600000 COOKIES MEXICAN WEDDING 8 CT This is Albertson's store recall (Albertsons Companies LLC)
  FoodClass IIReported June 10, 2026 · Contains statement does not declare Pecan
• UPC 22730900000 COOKIES COWBOY 18CT This is Albertson's store-made recall (Albertsons Companies LLC)
  FoodClass IIReported June 10, 2026 · Contains statement does not declare Pecan
• UPC 25185700000 COOKIE GOURMET DUBAI 1CT This is Alb recall (Albertsons Companies LLC)
  FoodClass IIReported June 10, 2026 · Contains statement does not declare Pistachio.
• UPC 25814700000 CAKE BOSTON CREME DUBAI 5IN recall (Albertsons Companies LLC)
  FoodClass IIReported June 10, 2026 · Contains statement does not declare Pistachio.
• UPC 22749800000 CAKE BOSTON ALMOND recall (Albertsons Companies LLC)
  FoodClass IIIReported June 10, 2026 · Contains statement does not declare Almond.
• UPC 25394400000 CAKE PISTACHIO SHAPED DESSERT 1CT recall (Albertsons Companies LLC)
  FoodClass IIIReported June 10, 2026 · Contains statement does not declare Pistachio.
• UPC 22394700000 Cake Almond Raspberry Pavillions 2-layer recall (Albertsons Companies LLC)
  FoodClass IIIReported June 10, 2026 · Contains statement does not declare Almond.
• UPC 25811100000 CAKE RASPBERRY MOON 8IN 2-layer. This is Albertson's store-made recall (Albertsons Companies LLC)
  FoodClass IIReported June 10, 2026 · Contains statement does not declare Almond.
• UPC 25491700000 Cake Pav Chocolate Lady Madeleines Strawberry. recall (Albertsons Companies LLC)
  FoodClass IIReported June 10, 2026 · Contains statement does not declare Almond.
• UPC 25139500000 Cake Cakerie Strawberry Shortcake Triangle. recall (Albertsons Companies LLC)
  FoodClass IIReported June 10, 2026 · Contains statement does not declare Hazelnut.
• UPC 22253500000 Cake Bar Artisan White Strawberry Small. recall (Albertsons Companies LLC)
  FoodClass IIReported June 10, 2026 · Contains statement does not declare Almond.
• UPC 22418000000 Platter Catering Loaf Cake Slice. Th recall (Albertsons Companies LLC)
  FoodClass IIReported June 10, 2026 · Contains statement does not declare Walnut.
• UPC 25216200000 Cheesecake Slice Colossal Dubai. This is A recall (Albertsons Companies LLC)
  FoodClass IIReported June 10, 2026 · Contains statement does not declare pistachio.
• UPC 28848900000 Cake Yellow Fudge Pecan 1/2 8IN This is Alberts recall (Albertsons Companies LLC)
  FoodClass IIIReported June 10, 2026 · Contains statement does not declare pecan.
• UPC 28832500000 Cake Yellow Caramel Pecan 1/2 8IN UPC 28831600000 Cake Ye recall (Albertsons Companies LLC)
  FoodClass IIIReported June 10, 2026 · Contains statement does not declare pecan.
• UPC 22679400000 CAKE CRAVIN CARROT 8IN 1-layer This is Albertson's recall (Albertsons Companies LLC)
  FoodClass IIReported June 10, 2026 · Contains statement does not declare pecan.
• UPC 22655200000 CAKE CARROT 8IN 2-Layer UPC 27813200000 CAKE recall (Albertsons Companies LLC)
  FoodClass IIReported June 10, 2026 · Contains statement does not declare pecan or walnut.
• SECOND NATURE KETO CRUNCH SMART MIX recall (SECOND NATURE BRAND)
  FoodClass IIReported June 10, 2026 · The product may contain undeclared allergens (cashews, pistachios), and dried cherries.
• Yunker recall (Sato Pharmaceutical Inc.)
  FoodClass IIIReported June 10, 2026 · Product does not meet label claim for Vitamin E.
• a2 Platinum Premium infant formula Milk-based Powder with Iron 31.7oz recall (The a2 Milk Company)
  FoodClass IReported June 10, 2026 · Possible contamination with Cereulide toxin.
• Xyvona recall (SUN PHARMACEUTICAL INDUSTRIES INC)
  DrugClass IIReported June 10, 2026 · Labeling: Not Elsewhere Classified. This recall has been initiated in response to the denial by FDA of marketing the product under the proprietary name Xyvona
• Xyvona recall (SUN PHARMACEUTICAL INDUSTRIES INC)
  DrugClass IIReported June 10, 2026 · Labeling: Not Elsewhere Classified. This recall has been initiated in response to the denial by FDA of marketing the product under the proprietary name Xyvona
• Niacin Extended-release Tablets recall (Lannett Company Inc.)
  DrugClass IIReported June 10, 2026 · Failed Dissolution Specifications: during 12M LT stability testing OOS low for Stage 3 dissolution at the 24-hour timepoint.
• TopCare health recall (Guardian Drug Co. Inc.)
  DrugClass IIReported June 10, 2026 · Presence of foreign substance: small metallic particles in chewable tablets.
• TopCare health recall (Guardian Drug Co. Inc.)
  DrugClass IIReported June 10, 2026 · Presence of foreign substance: small metallic particles in chewable tablets.
• EQUALINE ultra strength recall (Guardian Drug Co. Inc.)
  DrugClass IIReported June 10, 2026 · Presence of foreign substance: small metallic particles in chewable tablets.
• EQUALINE extra strength recall (Guardian Drug Co. Inc.)
  DrugClass IIReported June 10, 2026 · Presence of foreign substance: small metallic particles in chewable tablets.
• GOODSENSE Ultra Strength recall (Guardian Drug Co. Inc.)
  DrugClass IIReported June 10, 2026 · Presence of foreign substance: small metallic particles in chewable tablets.
• GOODSENSE Extra Strength recall (Guardian Drug Co. Inc.)
  DrugClass IIReported June 10, 2026 · Presence of foreign substance: small metallic particles in chewable tablets.
• H.E.B Extra Strength Calcium Carbonate Antacid Tablets recall (Guardian Drug Co. Inc.)
  DrugClass IIReported June 10, 2026 · Presence of foreign substance: small metallic particles in chewable tablets.
• HyVee recall (Guardian Drug Co. Inc.)
  DrugClass IIReported June 10, 2026 · Presence of foreign substance: small metallic particles in chewable tablets.
• HyVee recall (Guardian Drug Co. Inc.)
  DrugClass IIReported June 10, 2026 · Presence of foreign substance: small metallic particles in chewable tablets.
• Harris Teeter recall (Guardian Drug Co. Inc.)
  DrugClass IIReported June 10, 2026 · Presence of foreign substance: small metallic particles in chewable tablets.
• FAMILY WELLNESS recall (Guardian Drug Co. Inc.)
  DrugClass IIReported June 10, 2026 · Presence of foreign substance: small metallic particles in chewable tablets.
• FAMILY WELLNESS recall (Guardian Drug Co. Inc.)
  DrugClass IIReported June 10, 2026 · Presence of foreign substance: small metallic particles in chewable tablets.
• DISCOUNT drug mart recall (Guardian Drug Co. Inc.)
  DrugClass IIReported June 10, 2026 · Presence of foreign substance: small metallic particles in chewable tablets.
• CAREone recall (Guardian Drug Co. Inc.)
  DrugClass IIReported June 10, 2026 · Presence of foreign substance: small metallic particles in chewable tablets.
• CAREone recall (Guardian Drug Co. Inc.)
  DrugClass IIReported June 10, 2026 · Presence of foreign substance: small metallic particles in chewable tablets.
• MARKET BASKET ANTACID Calcium Carbonate 1000 mg recall (Guardian Drug Co. Inc.)
  DrugClass IIReported June 10, 2026 · Presence of foreign substance: small metallic particles in chewable tablets.
• 24/7 life BY 7-ELEVEN recall (Guardian Drug Co. Inc.)
  DrugClass IIReported June 10, 2026 · Presence of foreign substance: small metallic particles in chewable tablets.
• Extra strength Antacid Calcium Carbonate 750 mg recall (Guardian Drug Co. Inc.)
  DrugClass IIReported June 10, 2026 · Presence of foreign substance: small metallic particles in chewable tablets.
• Good Neighbor Pharmacy recall (Guardian Drug Co. Inc.)
  DrugClass IIReported June 10, 2026 · Presence of foreign substance: small metallic particles in chewable tablets.
• Good Neighbor Pharmacy recall (Guardian Drug Co. Inc.)
  DrugClass IIReported June 10, 2026 · Presence of foreign substance: small metallic particles in chewable tablets.
• HALEON CALCIUM CARBONATE TUMS ANTACID recall (Guardian Drug Co. Inc.)
  DrugClass IIReported June 10, 2026 · Presence of foreign substance: small metallic particles in chewable tablets.
• HALEON CALCIUM CARBONATE TUMS ANTACID recall (Guardian Drug Co. Inc.)
  DrugClass IIReported June 10, 2026 · Presence of foreign substance: small metallic particles in chewable tablets.
• KIRKLAND Signature recall (Guardian Drug Co. Inc.)
  DrugClass IIReported June 10, 2026 · Presence of foreign substance: small metallic particles in chewable tablets.
• Amlodipine and Olmesartan Medoxomil Tablets recall (Ascend Laboratories, LLC)
  DrugClass IIReported June 10, 2026 · Failed Dissolution Specifications: Olmesartan Medoxomil content below specifications
• Duloxetine DR Capsules recall (Asclemed USA Inc.)
  DrugClass IIReported June 10, 2026 · CGMP Deviations; presence of Nitrosamine Drug Substance Related Impurity (NDSRI), N-nitroso-duloxetine, above the FDA acceptable intake limit.
• Lidocaine HCl Injection USP recall (Spectra Medical Devices, Llc)
  DrugClass IIReported June 10, 2026 · Lack of Assurance of Sterility
• Lidocaine HCl Injection recall (Eugia US LLC)
  DrugClass IIIReported June 10, 2026 · Labeling: Not Elsewhere Classified: The label wrap covers the barcode, making it hard to scan
• Sharpoint 2.2MM recall (SSC- Surgical Specialties Corporation)
  Medical deviceClass IIReported June 10, 2026 · 3.0mm surgical knives labeled and packaged as 2.2mm surgical knives.
• TITANIUM/FLUOROPLASTIC PISTON 0.6MM DIA X 3.75MM L Model/Catalog Number: 409-375 ... recall (Grace Medical, Inc.)
  Medical deviceClass IIReported June 10, 2026 · Due to incorrect functional length on device labeling.
• Aligned Medical AMS16835 Fluids Kit RX recall (Windstone Medical Packaging, Inc.)
  Medical deviceClass IIReported June 10, 2026 · Lidocaine Hydrochloride Injection, USP, which was recalled by a supplier for quality issues, was included in custom convenience kits.
• MAC 5 A4 Resting ECG Analysis System 855001-001 recall (GE Medical Systems China Co., Ltd.)
  Medical deviceClass IIReported June 10, 2026 · Software in development inadvertently made available for customer use. Use of this software version can result in clinical information being associated with...
• DeRoyal Industries Inc. Ref 46-406 recall (DeRoyal Industries Inc)
  Medical deviceClass IIReported June 10, 2026 · Sterile wound dressing, lacks sterility assurance
• BD Pyxis MedBank Mini REF: 1147-00 Medication cabinet recall (CareFusion 303, Inc.)
  Medical deviceClass IIReported June 10, 2026 · Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
• BD Pyxis MedBank Tower REF: 1145-00 Medication cabinet recall (CareFusion 303, Inc.)
  Medical deviceClass IIReported June 10, 2026 · Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
• BD Pyxis MedStation ES Tower REF: 352 Medication cabinet recall (CareFusion 303, Inc.)
  Medical deviceClass IIReported June 10, 2026 · Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
• BD Pyxis Mini Main REF: 349 Medication cabinet recall (CareFusion 303, Inc.)
  Medical deviceClass IIReported June 10, 2026 · Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
• BD Pyxis Anesthesia Station 4000 REF: 338 Medication cabinet recall (CareFusion 303, Inc.)
  Medical deviceClass IIReported June 10, 2026 · Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
• BD Pyxis Anesthesia Station ES REF: 327 Medication cabinet recall (CareFusion 303, Inc.)
  Medical deviceClass IIReported June 10, 2026 · Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
• BD Pyxis MedStation ES REF: 323 Medication cabinet recall (CareFusion 303, Inc.)
  Medical deviceClass IIReported June 10, 2026 · Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
• BD Pyxis MedStation 4000 REF: 303 Medication cabinet recall (CareFusion 303, Inc.)
  Medical deviceClass IIReported June 10, 2026 · Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
• Phothera 200 recall (Daavlin Distributing Company)
  Medical deviceClass IIReported June 10, 2026 · Some of the Calibration/Output Certificates had the outputs reversed.
• Brand Name: HiResolution" Bionic Ear System Product Name: HiRes Ultra 3D CI HiFocus... recall (Advanced Bionics, LLC)
  Medical deviceClass IIReported June 10, 2026 · Due to incorrect shelf-life expiration date.
• Neptune Smart Docking Station recall (Stryker Corporation)
  Medical deviceClass IIReported June 10, 2026 · It has been identified that the impacted docking station (SN 2521008873) was not product released from manufacturing and may not have completed required...
• Covidien EndoStitch" Polysorb Single Use Loading Unit recall (Covidien, LP)
  Medical deviceClass IIReported June 10, 2026 · The presence of holes in the pouch may compromise the package s ability to maintain the sterile barrier and protect the product from environmental exposure.
• CASE v7.0 Cardiac Testing System Model no. 3031234-001 Product Code SU3 recall (GE Medical Systems Information Technologies Inc)
  Medical deviceClass IIReported June 10, 2026 · Electrical sparking may occur at the printer head. If the Electrostatic Discharge (ESD) printer brush becomes dislodged, electrical sparking at the printer...
• Design Options Spinal Tray Spinal Needle Anesthesia procedure kits: Material Description recall (B Braun Medical Inc)
  Medical deviceClass IReported June 10, 2026 · These procedure kits contain Bupivacaine Hydrochloride in Dextrose Injection, USP. The manufacturer of the Bupivacaine, Huons Co, Ltd., has issued a voluntary...
• Spinocan Spinal Needle procedure kits: Material Description recall (B Braun Medical Inc)
  Medical deviceClass IReported June 10, 2026 · These procedure kits contain Bupivacaine Hydrochloride in Dextrose Injection, USP. The manufacturer of the Bupivacaine, Huons Co, Ltd., has issued a voluntary...
• Spinal Needle procedure kits: Material Description recall (B Braun Medical Inc)
  Medical deviceClass IReported June 10, 2026 · These procedure kits contain Bupivacaine Hydrochloride in Dextrose Injection, USP. The manufacturer of the Bupivacaine, Huons Co, Ltd., has issued a voluntary...
• The Large Volume Pump recall (Fresenius Kabi USA, LLC)
  Medical deviceClass IIReported June 10, 2026 · Potential for the Cassette Loading Lever to break.
• Brand Name: B. BRAUN MEDICAL INC. Product Name: SESK UPMC DOUBLE CATHETER TRAY ... recall (B Braun Medical Inc)
  Medical deviceClass IIReported June 10, 2026 · B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL¿ Liquid Adhesive, that they have issued a voluntary recall...
• Brand Name: B. BRAUN MEDICAL INC. Product Name: CESK SHANDS JACKSONVILLE 20055717 ... recall (B Braun Medical Inc)
  Medical deviceClass IIReported June 10, 2026 · B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL¿ Liquid Adhesive, that they have issued a voluntary recall...
• Brand Name: B. BRAUN MEDICAL INC. Product Name: CESK RIVERSIDE HEALTH SYSTEM ... recall (B Braun Medical Inc)
  Medical deviceClass IIReported June 10, 2026 · B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL¿ Liquid Adhesive, that they have issued a voluntary recall...
• Brand Name: B. BRAUN MEDICAL INC. Product Name: LYNDON B JOHNSON HOSPITAL SPINAL EPID... recall (B Braun Medical Inc)
  Medical deviceClass IIReported June 10, 2026 · B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL¿ Liquid Adhesive, that they have issued a voluntary recall...
• Brand Name: B. BRAUN MEDICAL INC. Product Name: CESK HARRIS METHODIST Model/Catalog... recall (B Braun Medical Inc)
  Medical deviceClass IIReported June 10, 2026 · B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL¿ Liquid Adhesive, that they have issued a voluntary recall...
• Brand Name: B. BRAUN MEDICAL INC. Product Name: NES1725KFXL SPINAL EPID CLOSED TIP... recall (B Braun Medical Inc)
  Medical deviceClass IIReported June 10, 2026 · B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL¿ Liquid Adhesive, that they have issued a voluntary recall...
• Brand Name: B. BRAUN MEDICAL INC. Product Name: BPSK recall (B Braun Medical Inc)
  Medical deviceClass IIReported June 10, 2026 · B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL¿ Liquid Adhesive, that they have issued a voluntary recall...
• Brand Name: B. BRAUN MEDICAL INC Product Name: CESK NORTHSIDE ANESTHESIA TRAY ... recall (B Braun Medical Inc)
  Medical deviceClass IIReported June 10, 2026 · B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL¿ Liquid Adhesive, that they have issued a voluntary recall...
• COVIDIEN Shiley Tracheostomy Tube Cuffed with Inner Cannula REF 6FEN UDI-DI code:... recall (Covidien LLC)
  Medical deviceClass IIReported June 10, 2026 · Due to customer complaint regarding incorrect display box labeling.
• LVP software of the Ivenix Infusion System recall (Fresenius Kabi USA, LLC)
  Medical deviceClass IReported June 10, 2026 · Potential software anomaly that can cause the pump to report a false battery-health value (typically 69%) and trigger a battery-depletion alarm that will shut...
• Pediatric care bed recall (KAYSERBETTEN GMBH & CO. KG)
  Medical deviceClass IReported June 10, 2026 · If the adjustment functions of the hand control, as instructed in the Manual, are not locked with the provided key when the patient (child) is unattended...
• Vornado Air Recalls SRTH Small Room Tower Heaters Due to Fire Hazard
  Consumer productReported June 5, 2026 · The recalled heater's fan blade can detach from the motor shaft, which can cause the fan to slow or stop, leading to overheating and melting of the enclosure...
• SUNS International Recalls Residential Elevator Interlock Switches Due to Fall and Crushing Hazard; Risk of Death or Serious Injury
  Consumer productReported June 5, 2026 · The affected interlock switches can become stuck in a retracted position, allowing the exterior door to remain unlocked, posing a risk of death or serious...
• TOMY Recalls Boon NURSH 8 oz Reusable Baby Bottles Due to Choking Hazard; Sold at Walmart
  Consumer productReported June 5, 2026 · The hard plastic outer shell can bubble or partially peel off, resulting in loose pieces of film-like plastic that pose a choking hazard to young children.
• Pool Drain Covers Recalled Due to Risk of Serious Injury or Death from Entrapment and Drowning Hazards; Violates Virginia Graeme Baker Pool & Spa Safety Act; Sold on Amazon by Broqixin
  Consumer productReported June 5, 2026 · The recalled drain covers violate the entrapment protection standards of the Virginia Graeme Baker Pool and Spa Safety Act (VGBA), posing deadly entrapment and...
• Bicycle Helmets Recalled Due to Risk of Serious Injury or Death from Head Injury; Violates Mandatory Standard for Bicycle Helmets; Sold on Amazon by Gudook Outdoor Sports
  Consumer productReported June 5, 2026 · The recalled helmets violate the mandatory safety standard for bicycle helmets because the helmets do not comply with the impact attenuation and certification...
• Crenlux Pool Drain Covers Recalled Due to Risk of Serious Injury or Death from Entrapment and Drowning Hazards; Violates Virginia Graeme Baker Pool & Spa Safety Act; Sold on Amazon by Eicong
  Consumer productReported June 5, 2026 · The recalled drain covers violate the entrapment protection standards of the Virginia Graeme Baker Pool and Spa Safety Act (VGBA), posing deadly entrapment and...
• Tiny Land Children's Play Tents Recalled Due to Risk of Injury from Irritation to Skin and Eyes
  Consumer productReported June 5, 2026 · The recalled tents' fiberglass poles can shed fibers, posing an injury risk of skin and eye irritation.
• Little Grape Land Recalls Nursing Pillows Due to Risk of Serious Injury or Death from Suffocation; Violate Mandatory Standards for Nursing Pillows and Infant Support Cushions
  Consumer productReported June 5, 2026 · The recalled nursing pillows advertised for infant feeding and tummy time violate the mandatory safety standards for nursing pillows and infant support...
• Wyze Labs Recalls Solar Cam Pan Security Cameras Due to Risk of Serious Injury from Fire and Burn Hazards
  Consumer productReported June 5, 2026 · The recalled Wyze Solar Cam Pan security cameras' incorrect assembly instructions can lead consumers to accidentally puncture the lithium ion battery's metal...

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