The Recall Desk

Archive

May 2026 recalls

624 recalls were announced in May 2026.

What the numbers show

Critical
6
Severe
174
High
296
Moderate
138
Low
10

Of the 624 recalls this month scored against our rubric, 1% are Critical, 28% are Severe.

301–400 of 624

  • SevereFDA (Devices)·Z-2114-2026·2026-05-13

    Medline Surgical Convenience Kits recalled for sterilization calibration defect

    Medline Industries is recalling multiple surgical convenience kits because equipment used to sterilize and package the devices had calibration issues that may have affected sterility assurance. The devices were processed through validated sterilization cycles but the calibration problems could impact their sterility.

    Product
    See RES for complete list. Medline Convenience Kits: 1) SPINAL CDS, Model Number: CDS940087AG; 2) SPINAL CDS, Model Number: CDS940087AI; 3) TOTAL HIP CDS-LF, Model Number: CDS980832Q; 4) TOTAL HIP CDS-LF, Model Number: CDS980832R; 5) TOTAL HIP CDS-LF, Model Number: CDS980832S; 6)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0700-2026·2026-05-13

    Buttermilk powder recalled over potential Salmonella contamination in bulk bags

    Buttermilk Powder in 25 kg paper bags, packed under the BMP Extra Grade Standard label, is being recalled over potential Salmonella contamination. The action covers 19,841 lbs.

    Product
    Buttermilk Powder - paper bags 25 kg. (packed under 1 label: BMP Extra Grade Standard)
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Drugs)·D-0513-2026·2026-05-13

    DELFLEX Peritoneal Dialysis Solution Recall Due to Potential Sterility Issues

    Fresenius Medical Care is recalling DELFLEX Dextrose Peritoneal Dialysis Solution bags due to potential leaks from bag perforations that could compromise sterility. Affected patients should contact their healthcare provider immediately.

    Product
    DELFLEX, Dextrose Peritoneal Dialysis Solution with attached stay-safe Exchange Set for Intraperitoneal Dialysis Only, 2.5% DEX. LM/LC, 2L 5PK, Part Number 054-20222, Fresenius Medical Care North America, 920 Winter Street, Waltham, MA 02451.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2108-2026·2026-05-13

    Medline Labor and Delivery Kits Recalled for Sterilization Calibration Issues

    Medline Industries is recalling approximately 29,192 labor and delivery kits and OB packs due to calibration issues in sterilization equipment that may impact sterility assurance. The products were exposed to validated sterilization cycles, but the calibration problems potentially compromise sterile status.

    Product
    Medline Convenience Kits: 1) OB KIT, Model Number: DYKM2326; 2) KIT LABOR DELIVERY TUBAL LIGAT, Model Number: DYKMBNDL165; 3) KIT LABOR & DELIVERY D&C/D&E, Model Number: DYKMBNDL31; 4) KIT LABOR & DELIVERY CERCLAGE, Model Number: DYKMBNDL38; 5) KIT LABOR & DELIVERY CERCL
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2091-2026·2026-05-13

    Medline Convenience Kits Recalled for Sterilization Calibration Issues

    Medline is recalling multiple convenience kits used in catheterization labs and surgical procedures due to calibration issues with sterilization equipment that may affect sterility assurance. The affected kits were distributed nationwide.

    Product
    Medline Convenience Kits: 1) ANGIO PROCEDURE PACK, Model Number:00-401824AA; 2) ENDO KIT W/SYRINGE, Model Number:DYKE1743; 3) BGMC ANGIOGRAPHY PACK-LF, Model Number:DYNJ0800934D; 4) GENERAL ENDO PACK-LF, Model Number:DYNJ0842873J; 5) ANGIO PROCEDURE PACK, Model Number:DY
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V309000·2026-05-13

    Lucid Air rear-wheel drive inverters may fail and cut drive power

    Lucid is recalling certain 2024-2025 Air rear-wheel drive vehicles because the Gen 4 inverter may experience internal friction and become damaged, causing a loss of drive power.

    Product
    LUCID — LUCID AIR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1974-2026·2026-05-13

    Halyard CATH LAB Kit Due to Syringe Adapter Disconnection Risk

    AVID Medical is recalling the Halyard CATH LAB kit (Model SACL75-01) due to risk that a Medline syringe rotating adaptor may unwind during use, causing loose or complete disconnection between the syringe and manifold.

    Product
    Halyard CATH LAB kit. Model Number: SACL75-01.
    Category
    Medical Device
    Distribution
    7 states
  • SevereFDA (Devices)·Z-1976-2026·2026-05-13

    Halyard NEURO IR PERIPHERAL kit syringe adapter may disconnect

    AVID Medical is recalling the Halyard NEURO IR PERIPHERAL (PS 64405) kit because the Medline syringe rotating adapter may unwind during use, causing a loose or full disconnection between the syringe and manifold.

    Product
    Halyard NEURO IR PERIPHERAL (PS 64405) kit. Model Number: UINR44-01.
    Category
    Medical Device
    Distribution
    7 states
  • SevereFDA (Food)·H-0764-2026·2026-05-13

    Raw Farm shredded raw cheddar linked to multistate E. coli outbreak

    Raw Farm Raw Cheddar Simply Shredded Original in 8 oz packs is being recalled in connection with a multi-state outbreak of E. coli O157:H7.

    Product
    RAW FARM RAW CHEDDAR SIMPLY SHREDDED Original MADE WITH: WHOLE RAW MILK TRULY RAW - NEVER WARMED ABOVE 102F MADE IN THE USA KEEP REFRIGERATED INGREDIENTS: WHOLE RAW MILK, VEGETABLE RENNET, CULTURES, KOSHER SEA SALT Produced By: RAW FARM, LLC www.rawfarmusa.com 8 oz (227g) UPC: 8
    Category
    Food
    Distribution
    10 states
  • SevereFDA (Drugs)·D-0540-2026·2026-05-13

    Lactated Ringers Injection Recalled for Particulate Matter Contamination

    B. Braun Medical Inc. is recalling Lactated Ringer's Injection USP (1000 mL containers) due to the presence of particulate matter. The recall affects 95,412 containers distributed nationwide.

    Product
    LACTATED RINGERS — LACTATED RINGERS (SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, AND CALCIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0837-2026·2026-05-13

    Bulk cheese sauce seasoning may be contaminated with Salmonella

    A bulk seasoning for cheese sauce is being recalled because the product has the potential to be contaminated with Salmonella. The action covers 24,012 lbs.

    Product
    Bulk WN-976-782-1 Seasoning for Cheese Sauce, Net Wt. 43.50 lbs., in a brown kraft bag
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Devices)·Z-1936-2026·2026-05-13

    Beacon Tip Centimeter Sizing Catheter recalled for cracking marker bands

    Cook Incorporated is recalling Beacon Tip Centimeter Sizing Catheters because marker bands may crack or break, which could lead to device fragmentation, prolonged procedures, vessel injury, and in worst-case scenarios, life-threatening harm or death.

    Product
    Beacon Tip Centimeter Sizing Catheter RPN/GPN NR5.0-35-70-P-10S-0-CSC-20 G31213 NR5.0-35-100-P-10S-0-CSC-20 G31214 NR5.0-35-100-P-10S-PIG-CSC-20 G31216 NR5.0-35-70-P-10S-VCF-CSC-20 G31220 NR5.0-35-100-P-10S-VCF-CSC-20 G31221 Sizing catheters are single-use, sterile
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0698-2026·2026-05-13

    Non-fat dried milk powder totes recalled over potential Salmonella contamination

    Low Heat Non-Fat Dried Milk Powder supplied in plastic totes under five labels is being recalled over potential Salmonella contamination. The action covers 1,110,564 lbs.

    Product
    Low Heat Non-Fat Dried Milk Powder - plastic totes (NTE) 2200 lbs. (packed under 5 labels: Off Grade NFDM Variable; Grade A NFDM LH Basic; Grade A NFDM LH Green Loop rBST Free; Grade A NFDM LH Standard NC rBST Free; NFDM LH Variable Standard)
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Devices)·Z-1981-2026·2026-05-13

    Coronary angio packs recalled over Medline syringe rotating adaptor defect

    Coronary angio convenience kits are being recalled because they contain Medline Namic syringes whose rotating adaptor may unwind, risking disconnection from the manifold.

    Product
    Convenience kits containing Medline Namic Angiographic Control Syringes with Rotating Adaptor CORONARY ANGIO PACK Model numbers ANCA80AP ANCA80AQ
    Category
    Medical Device
    Distribution
    1 state
  • SevereFDA (Devices)·Z-1977-2026·2026-05-13

    Halyard PERC TRAY Kit Syringe Adaptor Connection Risk Recall

    The Halyard PERC TRAY kit (models SLPC34-01 and SLPC34-02) is being recalled due to risk that a Medline syringe rotating adaptor may unwind during use, causing a loose or full disconnection between the syringe and manifold.

    Product
    Halyard PERC TRAY kit. Model Numbers: SLPC34-01, SLPC34-02.
    Category
    Medical Device
    Distribution
    7 states
  • SevereFDA (Drugs)·D-0518-2026·2026-05-13

    BD PurPrep Povidone-Iodine Topical Solution Sterility Assurance Recall

    CareFusion 213, LLC is recalling BD PurPrep (povidone-iodine 8.3% with isopropyl alcohol 72.5%) due to lack of assurance of sterility and potential product contamination. Affected lots are distributed nationwide.

    Product
    PURPREP — PURPREP (POVIDONE IODINE AND ISOPROPYL ALCOHOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2106-2026·2026-05-13

    Medline Convenience Kits recalled due to sterilization equipment calibration issues

    Medline Industries is recalling four Convenience Kit models (892 units) nationwide because sterilization and packaging equipment calibration issues may have compromised the sterility assurance level of the devices.

    Product
    Medline Convenience Kits: 1) CHEST TUBE INSERTION TRAY, Model Number: DYNDA2941A; 2) CHEST/BREAST-LF, Model Number: DYNJ83950; 3) HERNIA REPAIR TOTE, Model Number: DYNJ908337A; 4) HERNIA REPAIR TOTE, Model Number: DYNJ908337C
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2064-2026·2026-05-13

    Endoscopy Pump Tubing/Cap Set water aspiration risk recall

    Erbe Medical is recalling ERBEFLO 2 Endoscopy Pump Tubing/Cap Sets due to a connector design that may allow unintended water flow, potentially leading to water aspiration and serious respiratory conditions.

    Product
    ERBEFLO 2, Endoscopy Pump Tubing/Cap Set, REF: 20325-222
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0709-2026·2026-05-13

    Darkside of the Hive creamed honey may contain metal and plastic

    Darkside of the Hive creamed and whipped honey products are being recalled because they may contain stainless steel dust or flakes and small particles or shreds of plastic.

    Product
    Darkside of the Hive Creamed Honey/Salted Chocolate Creamed Honey 671333101414 *These product labels may also say Whipped Honey instead of Creamed Honey as labels and size were changed in this timeline from 14 oz Creamed Honey to 11 oz Whipped Honey. The UPC codes remained th
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·H-0767-2026·2026-05-13

    Lundberg Family Farms jasmine white rice may contain foreign materials

    Lundberg Family Farms White Rice Jasmine in 32 oz packages is being recalled over potential contamination with foreign materials. 27,324 packages are affected.

    Product
    LUNDBERG FAMILY FAMRS WHITE RICE JASMINE NET WT 32 OZ (2 lb) 907 g Manufactured and Distributed by: Lundberg Family Farms Richvale, CA 95974 UPC: 073416040281
    Category
    Food
    Distribution
    12 states
  • HighFDA (Devices)·Z-2050-2026·2026-05-13

    Prodisc C SK Cervical Implant Size Labeling Mix-Up Recall

    Centinel Spine is recalling Prodisc C SK U.S. cervical disc implants due to a labeling mix-up: 6mm products were labeled as 5mm and 5mm products were labeled as 6mm, creating risk of implanting the wrong size.

    Product
    Prodisc C SK U.S. IMPLANT EXTRA LARGE 5MM. Model: PDSXL5 Total cervical disc replacement.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0719-2026·2026-05-13

    Loard's brownie nut fudge ice cream has five undeclared allergens

    Loard's Brownie Nut Fudge Ice Cream in 32 oz tubs is being recalled because milk, walnuts, eggs, wheat and soy are undeclared on the label. 78 units are affected.

    Product
    Loard's Brownie Nut Fudge Ice Cream - 32 oz
    Category
    Food
    Distribution
    1 state
  • HighNHTSA·26E030000·2026-05-13

    Hale Recalls Weldon UV800 Display Units for Emergency Equipment Failure

    Hale Products Inc is recalling Weldon UV800 Display Units that may fail to power on or respond to touch, preventing the activation of emergency lights and firefighting equipment.

    Product
    EQUIPMENT:EMERGENCY:FIRE SUPRESSION recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2127-2026·2026-05-13

    Medline Arthroscopy Convenience Kits Recalled Due to Sterilization Equipment Calibration

    Medline is recalling five models of arthroscopy convenience kits due to calibration issues with sterilization equipment that may affect the sterility assurance level of the devices.

    Product
    Medline Convenience Kits: 1) ARTHROSCOPY CDS, Model Number: CDS984609B; 2) ARTHROSCOPY TRAYS, Model Number: DYNJ22501G; 3) ARTHROSCOPY PACK, Model Number: DYNJ32715F; 4) CHS ARTHROSCOPY PACK, Model Number: DYNJ50834C; 5) ARTHROSCOPY TRAY-LF, Model Number: DYNJ51069
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0701-2026·2026-05-13

    Fain's blackberry honey spread may contain metal and plastic fragments

    Fain's Blackberry Honey Spread in 12 oz jars is being recalled because it may contain stainless steel dust or flakes and small particles or shreds of plastic.

    Product
    Fain s Blackberry Honey Spread, 12oz net wt., UPC 01832213862
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·H-0708-2026·2026-05-13

    Darkside of the Hive natural creamed honey may contain metal fragments

    Natural Creamed Honey from Darkside of the Hive is being recalled because it may contain stainless steel dust or flakes and small particles or shreds of plastic.

    Product
    Natural Creamed Honey, 671333101377 *These product labels may also say Whipped Honey instead of Creamed Honey as labels and size were changed in this timeline from 14 oz Creamed Honey to 11 oz Whipped Honey. The UPC codes remained the same. Packaged in Glass jars UPC Code: 6
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·H-0706-2026·2026-05-13

    Walker Honey Hatch creamed honey may contain metal and plastic fragments

    Hatch Creamed Honey from Walker Honey Co is being recalled because it may contain stainless steel dust or flakes and small particles or shreds of plastic.

    Product
    Hatch Creamed Honey 671333101339 * These product labels may also say Whipped Honey instead of Creamed Honey as labels and size were changed in this timeline from 14 oz Creamed Honey to 11 oz Whipped Honey. The UPC codes remained the same. Packaged in Glass jars UPC Code: 6
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·H-0753-2026·2026-05-13

    Loard's toasted almond ice cream has undeclared milk and almonds

    Loard's Toasted Almond Ice Cream in 32 oz tubs is being recalled because milk and almonds are undeclared on the label. 656 units are affected.

    Product
    Loard's Toasted Almond Ice Cream - 32 oz
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·H-0723-2026·2026-05-13

    Loard's caramel cashew ice cream has undeclared milk, cashews and soy

    Loard's Caramel Cashew Ice Cream in 32 oz tubs is being recalled because milk, cashews, soy and sulfites are undeclared on the label. 332 units are affected.

    Product
    Loard's Caramel Cashew Ice Cream - 32 oz
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·H-0715-2026·2026-05-13

    Loard's black raspberry marble ice cream has undeclared milk and colors

    Loard's Black Raspberry Marble Ice Cream in 32 oz tubs is being recalled because milk, Red #40 and Blue #1 are undeclared on the label. 362 units are affected.

    Product
    Loard's Black Raspberry Marble Ice Cream - 32 oz
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·H-0741-2026·2026-05-13

    Loard's mocha chip ice cream recalled over undeclared milk

    Loard's Mocha Chip Ice Cream in 32 oz and 56 oz tubs is being recalled because milk is undeclared on the label.

    Product
    Loard's Mocha Chip Ice Cream - 32 oz; 56 oz
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·H-0734-2026·2026-05-13

    Loard's green tea ice cream has undeclared milk and Yellow #5

    Loard's Green Tea Ice Cream in 32 oz tubs is being recalled because milk and Yellow #5 are undeclared on the label. 436 units are affected.

    Product
    Loard's Green Tea Ice Cream - 32 oz
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-2093-2026·2026-05-13

    Medline Cardiac Surgery Kits Recalled Due to Sterilization Equipment Calibration Issues

    Medline Industries is recalling cardiac surgery convenience kits because sterilization and packaging equipment calibration issues may have affected the sterility assurance level of the devices.

    Product
    See RES for complete list. Medline Convenience Kits: 1) OPEN HEART CDS, Model Number:CDS840015AQ; 2) OPEN HEART CDS, Model Number:CDS840015AQ; 3) OPEN HEART CDS, Model Number:CDS840023T; 4) OFF PUMP CABG CDS, Model Number:CDS840087AI; 5) OFF PUMP CABG CDS, Model Number:CDS840087A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2116-2026·2026-05-13

    Medline Basic Nerve Block Tray sterilization calibration issue

    Medline is recalling Basic Nerve Block Trays due to calibration issues with sterilization equipment that may have compromised the sterility assurance level of the devices.

    Product
    Medline Convenience Kits: 1) BASIC NERVE BLOCK TRAY W/LINEN, Model Number:PAIN0150C
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2067-2026·2026-05-13

    BioFire Joint Infection Panel diagnostic test kit contamination recall

    BioFire Diagnostics is recalling its Joint Infection (JI) Panel diagnostic test kits due to contamination that may produce false positive results.

    Product
    BioFire Joint Infection (JI) Panel REF: RFIT-ASY-0138, 30 test Kit.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2124-2026·2026-05-13

    Medline Convenience Kits recalled due to sterilization calibration issues

    Medline Industries is recalling two models of Convenience Kits because calibration problems with sterilization and packaging equipment may have compromised the sterility of the products.

    Product
    Medline Convenience Kits: 1) DRAPE PACK, Model Number: DYNJ35363A; 2) SICK KIDS-GENERAL CUSTOM SPLIT, Model Number: SPTPCD10005
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2125-2026·2026-05-13

    Medline Convenience Kits recalled due to sterilization equipment calibration issues

    Medline Industries is recalling three models of medical trays due to calibration issues with sterilization equipment that may affect sterility assurance. The recall affects LVAD Driveline Trays and Central Line Dressing Change Trays distributed nationwide.

    Product
    Medline Convenience Kits: 1) LVAD DRIVELINE TRAY, Model Number: DM1035; 2) LVAD DRIVELINE TRAY, Model Number: DM1035A; 3) CENTRAL LINE DRESSING CHANGE TRAY, Model Number: DT8670A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2081-2026·2026-05-13

    BioFire Spotfire Respiratory/Sore Throat Panel Recall for False Negatives

    BioFire Diagnostics, LLC is recalling the Spotfire Respiratory/Sore Throat Panel due to false negative test results and control failures that may not accurately detect infections.

    Product
    Biofire Spotfire Respiratory/Sore Throat Panel REF: 423485
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2110-2026·2026-05-13

    Medline Convenience Kits for C-Section and Obstetric Procedures

    Medline Industries is recalling 12,529 units of sterile surgical convenience kits used in cesarean section and obstetric procedures worldwide due to equipment calibration issues that may compromise sterilization assurance.

    Product
    Medline Convenience Kits: 1) C-SECTION PACK, Model Number: CDS820080N; 2) C-SECTION CDS, Model Number: CDS983523G; 3) C-SECTION, Model Number: CDSCCR611O; 4) C-SECTION, Model Number: CDSCCR611P; 5) LUD C-SECTION-LF, Model Number: DYNJ0101616I; 6) C-SECTION TRAY, Model
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0694-2026·2026-05-13

    Woodstock organic shelled edamame may contain metal pieces

    Woodstock Organic Shelled Edamame in 10 oz and 48 oz bags is being recalled because the product may contain metal pieces. 7,160 cases are affected.

    Product
    Woodstock Organic Shelled Edamame 10 oz. and 48 oz.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0742-2026·2026-05-13

    Loard's orange sherbert has undeclared milk and Yellow #5

    Loard's Orange Sherbert in 32 oz tubs is being recalled because milk and Yellow #5 are undeclared on the label. 150 units are affected.

    Product
    Loard's Orange Sherbert - 32 oz
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-2107-2026·2026-05-13

    Medline Neurosurgical Convenience Kits Sterilization Calibration Defect

    Medline is recalling 52 models of neurosurgical convenience kits due to calibration issues with sterilization equipment that may have compromised the sterility assurance level of the products.

    Product
    Medline Convenience Kits: 1) NEURO SHUNT- CODMAN, Model Number: CDS860018G; 2) NEURO SHUNT- CODMAN, Model Number: CDS860018I; 3) KIT NEUR FUS LUM POST CRANDALL, Model Number: DYKMBNDL138; 4) KIT NEURO FUS LUM POST SANSUR, Model Number: DYKMBNDL142; 5) KIT NEURO FUS LUM P
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0747-2026·2026-05-13

    Loard's pumpkin ice cream has undeclared milk and Yellow #6

    Loard's Pumpkin Ice Cream in 32 oz tubs is being recalled because milk and Yellow #6 are undeclared on the label. 294 units are affected.

    Product
    Loard's Pumpkin Ice Cream - 32 oz
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·H-0710-2026·2026-05-13

    Hatch green chile creamed honey may contain metal and plastic fragments

    Hatch Green Chile Creamed Honey from Darkside of the Hive is being recalled because it may contain stainless steel dust or flakes and small particles or shreds of plastic.

    Product
    Hatch Green Chile Creamed Honey 671333101339 * These product labels may also say Whipped Honey instead of Creamed Honey as labels and size were changed in this timeline from 14 oz Creamed Honey to 11 oz Whipped Honey. The UPC codes remained the same. Packaged in Glass jars
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·H-0735-2026·2026-05-13

    Loard's horchata ice cream has undeclared milk and soy

    Loard's Horchata Ice Cream in 32 oz tubs is being recalled because milk and soy are undeclared on the label. 450 units are affected.

    Product
    Loard's Horchata Ice Cream - 32 oz
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·H-0731-2026·2026-05-13

    Loard's coffee ice cream recalled over undeclared milk

    Loard's Coffee Ice Cream in 32 oz tubs is being recalled because milk is undeclared on the label. 790 units are affected.

    Product
    Loard's Coffee Ice Cream - 32 oz
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·H-0690-2026·2026-05-13

    Montebianco vegan base recalled over milk above acceptable allergen levels

    Montebianco Base Vegan is being recalled because the milk allergen present was found to exceed acceptable levels despite the product carrying only a "May contain milk" statement.

    Product
    Montebianco, 113542 Base Vegan, 2 Kg (4.41 Lb) Bag, packed 8 bags per master case of 2 Kg (4.41 lb) each total case weight,16 Kg / 35.27 lb
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-2051-2026·2026-05-13

    Prodisc C SK cervical disc implant labeling mix-up recalled

    Centinel Spine is recalling Prodisc C SK U.S. Implant Extra Large cervical disc replacement devices due to a labeling mix-up where 6mm implants were labeled as 5mm and 5mm implants were labeled as 6mm.

    Product
    Prodisc C SK U.S. IMPLANT EXTRA LARGE 6MM. Model Number: PDSXL6. Total cervical disc replacement.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2092-2026·2026-05-13

    Medline Convenience Kits sterilization and packaging calibration issues recalled

    Medline Industries is recalling multiple Convenience Kit models used in cardiac, vascular, and surgical procedures due to calibration issues with sterilization and packaging equipment that could impact sterility assurance. Approximately 39,341 units distributed worldwide may be affected.

    Product
    Medline Convenience Kits: 1) ANGIO PROCEDURE PACK, Model Number:00-401824AB; 2) OR ARTERIOGRAM, Model Number:CDS985094F; 3) INTRAVASOR CATH KIT, Model Number:DYK1060193I; 4) KIT SURG ONC LAP DIAG/CV CATH, Model Number:DYKMBNDL153; 5) KIT ACES INSERT PERCUTANEOUS T, Model
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2121-2026·2026-05-13

    Medline Convenience Kits General Closure sterilization calibration issue

    Medline Industries is recalling Convenience Kits (Model DYKMBNDL200A) due to calibration issues in sterilization equipment that may have compromised sterility assurance. The kits were distributed nationwide.

    Product
    Medline Convenience Kits: 1) KIT GENERAL CLOSURE, Model Number: DYKMBNDL200A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2063-2026·2026-05-13

    ERBEFLO CleverCap Endoscope Tubing Sets Recalled for Water Aspiration Risk

    Erbe Medical is recalling ERBEFLO CleverCap hybrid tubing and cap sets for endoscopes due to a connector configuration that may allow unintended water flow, potentially leading to water aspiration and serious respiratory complications.

    Product
    ERBEFLO CleverCap: Hybrid Tubing/Cap Set for Olympus Scopes, 20325-201; ERBEFLO CleverCap Hybrid Tubing/Cap Set for Fujifilm Scopes, REF: 20325-203;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2065-2026·2026-05-13

    Physio-Control Defibrillators May Lack Required Performance Inspection

    Physio-Control defibrillators (LIFEPAK 15, 1000, 35, and 20e models) serviced between July 2023 and November 2025 may not have undergone required Performance Inspection Procedures, potentially preventing therapy delivery.

    Product
    LIFEPAK 15, REF: 99577-000025, 99577-000047, 99577-001256, 99577-001217, 99577-001241, 99577-001255, 99577-001219, 99577-001957, 99577-001935, 99577-001964, 99577-001955, 99577-001956, 99577-001588, 99577-001958, 99577-001950, 99577-001962, 99577-002178, 99577-001372, 99577-00193
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2119-2026·2026-05-13

    Medline Convenience Kits medical devices recalled due to sterilization calibration issues

    Medline is recalling Convenience Kits (Model DYNJ50806L) because equipment calibration issues may have affected the sterility assurance level of the devices. The products were exposed to sterilization and packaging cycles but the calibration problems could impact their sterility.

    Product
    Medline Convenience Kits: 1) WMC I D PACK-LF, Model Number: DYNJ50806L
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0754-2026·2026-05-13

    Loard's ube ice cream has undeclared milk and four colors

    Loard's Ube Ice Cream in 32 oz tubs is being recalled because milk, Red #3, Red #40, Blue #1 and Blue #2 are undeclared on the label. 1,568 units are affected.

    Product
    Loard's Ube Ice Cream - 32 oz
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-2101-2026·2026-05-13

    Medline Medical Device Convenience Kits Sterilization Calibration Recall

    Medline Industries is recalling multiple Convenience Kit medical devices due to calibration issues in sterilization and packaging equipment that may affect sterility assurance. The devices were distributed nationwide.

    Product
    See RES for complete list. Medline Convenience Kits: 1) DRAWER 6-IV FLUIDS GLOVES, Model Number: ACC010326; 2) DRAWER 6-IV FLUIDS GLOVES, Model Number: ACC010326A; 3) DRAWER 6-IV FLUIDS GLOVES, Model Number: ACC010326B; 4) DRAWER #5, Model Number: ACC010475; 5) DRAWER 1 NEURO CAR
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2095-2026·2026-05-13

    Medline Convenience Kits recalled due to sterilization calibration issues

    Medline Industries is recalling multiple convenience kits used in surgical and biopsy procedures due to calibration issues with sterilization equipment that may affect sterility assurance. The recall affects 4,064 units distributed nationwide.

    Product
    Medline Convenience Kits: 1) KIT SURG ONC EXCISION BREAST, Model Number:DYKMBNDL84A; 2) KIT SURG ONC EXPLORATORY LAP, Model Number:DYKMBNDL87A; 3) CT BIOPSY TRAY, Model Number:DYNDH1143C; 4) BIOPSY SPECIALS PACK, Model Number:DYNDH1873; 5) BIOPSY SPECIALS PACK, Model Num
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2123-2026·2026-05-13

    Medline Triple Lumen Insertion Kits Recalled for Sterilization Calibration

    Medline Industries is recalling Triple Lumen Insertion Kits (Model DYNDM1031A) due to calibration issues with sterilization equipment that may have compromised the sterility assurance level of the products.

    Product
    Medline Convenience Kits: 1) KIT TRIPLE LUMEN INSERTION, Model Number: DYNDM1031A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2103-2026·2026-05-13

    Medline Convenience Kits Recalled Over Sterilization Calibration Issues

    Medline is recalling three models of medical convenience kits (central line, LVAD driveline, and surgical oncology) distributed nationwide due to calibration issues in sterilization equipment that may have reduced sterility assurance.

    Product
    Medline Convenience Kits: 1) CENTRAL LINE UNIVERSAL INSERTI, Model Number: CVI3780; 2) LVAD DRIVELINE TRAY, Model Number: DM1035; 3) KIT SURG ONC INSERT CENT.VENOU, Model Number: DYKMBNDL43
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2104-2026·2026-05-13

    Medline PPE Kit recalled for sterilization calibration issues

    Medline is recalling Convenience Kits (PPE Kit, Model DYK1011945P) due to calibration issues with sterilization and packaging equipment that may compromise sterility assurance. The product was distributed nationwide.

    Product
    Medline Convenience Kits: 1) PPE KIT, Model Number: DYK1011945P
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2113-2026·2026-05-13

    Medline Convenience Kits Surgical Packaging Sterilization Calibration Issue

    Medline Industries is recalling over 7,700 surgical convenience kits due to calibration issues with sterilization and packaging equipment that may affect the sterility assurance level of the products.

    Product
    Medline Convenience Kits: 1) KIT OPHTHALMIC RUPTURE GLOBE, Model Number: DYKMBNDL104; 2) KIT OPHTHALMIC RUPTURE GLOBE, Model Number: DYKMBNDL104A; 3) KIT OPHTHALMOLOGY CORNEAL TRAN, Model Number: DYKMBNDL159; 4) KIT OPHTHALMOLOGY CATARACT, Model Number: DYKMBNDL180; 5) K
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2098-2026·2026-05-13

    Medline Surgical Convenience Kits Recalled for Sterilization Calibration Issues

    Medline Industries is recalling 114,778 surgical convenience kits due to calibration issues with sterilization equipment that may affect the sterility assurance level of the products. No illnesses or injuries have been reported.

    Product
    See RES for complete list. Medline Convenience Kits: 1) MAJOR LAPAROTOMY CDS, Model Number: CDS860015U; 2) MAJOR LAPAROTOMY CDS, Model Number: CDS860015V; 3) MAJOR LAPAROTOMY CDS, Model Number: CDS860015W; 4) MAJOR LAPAROTOMY CDS, Model Number: CDS860015X; 5) MINOR LAPAROTOMY CDS
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0776-2026·2026-05-13

    Publix bran flakes cereal recalled over plastic foreign material

    Publix Bran Flakes Wheat Cereal in 18 oz boxes is being recalled because of foreign material, specifically plastic. 13,824 units are affected.

    Product
    Publix Bran Flakes, Wheat Cereal. Net Wt 18oz (1 lb 2 oz) 510g. UPC 0 41415-24305 7. Distributed by Publix Super Markets, Inc. Lakeland, FL 33802.
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·H-0752-2026·2026-05-13

    Loard's strawberry ice cream has undeclared milk and Red #40

    Loard's Strawberry Ice Cream in 32 oz and 56 oz tubs is being recalled because milk and Red #40 are undeclared on the label.

    Product
    Loard's Strawberry Ice Cream - 32 oz; 56 oz
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·H-0704-2026·2026-05-13

    Darkside of the Hive cinnamon creamed honey may contain metal fragments

    Cinnamon Creamed Honey from Darkside of the Hive is being recalled because it may contain stainless steel dust or flakes and small particles or shreds of plastic.

    Product
    Cinnamon Creamed Honey 671333101360 * These product labels may also say Whipped Honey instead of Creamed Honey as labels and size were changed in this timeline from 14 oz Creamed Honey to 11 oz Whipped Honey. The UPC codes remained the same. Packaged in Glass jars UPC: 6713
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·H-0760-2026·2026-05-13

    Chocolate Showers ice cream recalled over undeclared soy

    Chocolate Showers Ice Cream, sold under five store labels, is being recalled because soy is undeclared on the label. 1,396 units are affected.

    Product
    Chocolate Showers Ice Cream - 32 oz (5 labels: Mollie Stone's; Dehoff's; Farmer Joe's, Piazza's Fine Foods, and Berkeley Bowl) UPC: 8-12017-00918
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·H-0744-2026·2026-05-13

    Loard's pecan praline ice cream has undeclared milk and pecans

    Loard's Pecan Praline Ice Cream in 32 oz tubs is being recalled because milk and pecans are undeclared on the label. 875 units are affected.

    Product
    Loard's Pecan Praline Ice Cream - 32 oz
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·H-0703-2026·2026-05-13

    Darkside of the Hive blackberry creamed honey may contain metal fragments

    Blackberry Creamed Honey from Darkside of the Hive is being recalled because it may contain stainless steel dust or flakes and small particles or shreds of plastic.

    Product
    Blackberry Creamed Honey 671333101308 * These product labels may also say Whipped Honey instead of Creamed Honey as labels and size were changed in this timeline from 14 oz Creamed Honey to 11 oz Whipped Honey.The UPC codes remained the same. Packaged in Glass jars UPC Code:
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·H-0755-2026·2026-05-13

    Loard's Vanilla Ice Cream Recalled for Undeclared Milk

    Loard's Vanilla Ice Cream in 32 oz and 56 oz containers is being recalled because it contains milk that is not listed on the label.

    Product
    Loard's Vanilla Ice Cream - 32 oz; 56 oz
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·H-0702-2026·2026-05-13

    Walker Honey raspberry creamed honey may contain metal fragments

    Raspberry Creamed Honey from Walker Honey Co is being recalled because it may contain stainless steel dust or flakes and small particles or shreds of plastic.

    Product
    Raspberry Creamed Honey 671333101322 ¿ These product labels may also say Whipped Honey instead of Creamed Honey as labels and size were changed in this timeline from 14 oz Creamed Honey to 11 oz Whipped Honey, UPC Code: 671333101322
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·H-0737-2026·2026-05-13

    Loard's lime sherbert has undeclared milk, wheat, soy and colors

    Loard's Lime Sherbert in 32 oz tubs is being recalled because milk, wheat, soy, Yellow #5 and Green #3 are undeclared on the label. 110 units are affected.

    Product
    Loard's Lime Sherbert - 32 oz
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·H-0718-2026·2026-05-13

    Loard's blueberry cheesecake ice cream has undeclared milk and colors

    Loard's Blueberry Cheesecake Ice Cream in 32 oz tubs is being recalled because milk, Red #40 and Blue #1 are undeclared on the label. 200 units are affected.

    Product
    Loard's Blueberry Cheesecake Ice Cream - 32 oz
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·H-0714-2026·2026-05-13

    Loard's banana ice cream has undeclared milk and Yellow #5

    Loard's Banana Ice Cream in 32 oz and 56 oz tubs is being recalled because milk and Yellow #5 are undeclared on the label.

    Product
    Loard's Banana Ice Cream - 32 oz; 56 oz
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-2090-2026·2026-05-13

    Medline Convenience Kits recalled for potential sterilization compromise

    Medline Industries is recalling eight models of Convenience Kits due to calibration issues with sterilization equipment that may have affected the sterility assurance level of the devices.

    Product
    Medline Convenience Kits: 1) SCC RF PAIN MGMT, Model Number:DYNJ56436A; 2) SCC RF PAIN MGMT, Model Number:DYNJ56436B; 3) SCC RF PAIN MGMT, Model Number:DYNJ56436C; 4) CPNB SETUP TRAY, Model Number:DYNJRA1979; 5) CPNB SETUP TRAY, Model Number:DYNJRA1979A; 6) CPNB SETUP
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2046-2026·2026-05-13

    da Vinci X and Xi Surgical Systems Recalled for Manipulator Arm Screw Breakage

    Intuitive Surgical is recalling certain Universal Surgical Manipulator arm sub-assemblies in da Vinci X and Xi Surgical Systems due to screws that may be susceptible to breaking during use.

    Product
    Brand Name: Da Vinci X and Da Vinci Xi Product Name: da Vinci X, Xi Surgical System Model/Catalog Number: IS4000; IS4200 Software Version: N/A Product Description: he da Vinci Xi, X Surgical systems each consist of three main components: the Surgeon Console (SC), the Vision
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0716-2026·2026-05-13

    Loard's black raspberry ice cream has undeclared milk and colors

    Loard's Black Raspberry Ice Cream in 32 oz tubs is being recalled because milk, Red #40 and Blue #1 are undeclared on the label. 446 units are affected.

    Product
    Loard's Black Raspberry Ice Cream - 32 oz
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·H-0738-2026·2026-05-13

    Loard's mango ice cream has undeclared milk and Yellow #5

    Loard's Mango Ice Cream in 32 oz and 56 oz tubs is being recalled because milk and Yellow #5 are undeclared on the label.

    Product
    Loard's Mango Ice Cream - 32 oz; 56 oz
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·H-0717-2026·2026-05-13

    Loard's black walnut ice cream has undeclared milk and walnuts

    Loard's Black Walnut Ice Cream in 32 oz and 56 oz tubs is being recalled because milk and walnuts are undeclared on the label.

    Product
    Loard's Black Walnut Ice Cream - 32 oz; 56 oz
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·H-0761-2026·2026-05-13

    Good & Gather teriyaki chicken has undeclared sesame and soy

    Good & Gather Sesame Teriyaki Chicken with Rice sold at Target is being recalled because sesame and soy are undeclared allergens. 558 units are affected.

    Product
    Good & Gather Fresh from Our Deli. Sesame Teriyaki Chicken with Rice. Net Wt 18.0 oz (1.125lb). Keep Refrigerated. DPCI # 878-02-0227. UPC (01) 00250086000009 (3922) 00999. Distributed by SuperTarget Mpls, MN 55403.
    Category
    Food
    Distribution
    22 states
  • HighFDA (Food)·H-0748-2026·2026-05-13

    Loard's rainbow sherbert has undeclared milk, soy and three colors

    Loard's Rainbow Sherbert in 32 oz tubs is being recalled because milk, soy, Yellow #5, Red #40 and Green #3 are undeclared on the label. 252 units are affected.

    Product
    Loard's Rainbow Sherbert - 32 oz
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·H-0749-2026·2026-05-13

    Loard's raspberry sherbert has undeclared milk and Red #40

    Loard's Raspberry Sherbert in 32 oz tubs is being recalled because milk and Red #40 are undeclared on the label. 132 units are affected.

    Product
    Loard's Raspberry Sherbert - 32 oz
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·H-0725-2026·2026-05-13

    Loard's cherry vanilla ice cream has undeclared milk and Red #40

    Loard's Cherry Vanilla Ice Cream in 32 oz tubs is being recalled because milk and Red #40 are undeclared on the label. 484 units are affected.

    Product
    Loard's Cherry Vanilla Ice Cream - 32 oz
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-2096-2026·2026-05-13

    Medline Convenience Kits Recalled for Sterilization Equipment Calibration

    Medline is recalling certain Dental Pack and Surgical Pack convenience kits due to calibration issues with sterilization equipment that may affect sterility assurance. Approximately 3,508 units were distributed nationwide.

    Product
    Medline Convenience Kits: 1) DYNDA3003, Model Number: DENTAL PACK; 2) DYNJ87157, Model Number: GULLO SURGICAL PACK
    Category
    Medical Device
    Distribution
    Distributed nationwide

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