All US Product Recalls

Filters

Clear filters

• 4/5SevereFDA (Devices)·Z-2118-2026·2026-05-13

  Medline Convenience Kits recalled for potential sterility assurance defects

  Medline Industries is recalling six models of medical device convenience kits due to calibration issues with sterilization and packaging equipment that may have reduced sterility assurance levels. The recall affects 553 units distributed nationwide.

  Product

  Medline Convenience Kits: 1) PICC CATHETER INSERTION TRAY, Model Number: CVI4300; 2) OSC SHERMAN KNEE ARTHRO BASIC, Model Number: DYKM1977C; 3) KIT ACES INSERT PEG, Model Number: DYKMBNDL130; 4) KIT ACES INSERT PEG, Model Number: DYKMBNDL130A; 5) KIT ACES INSERT PERCUTAN

  Category

  Medical Device

  Distribution

  Distributed nationwide

• 4/5SevereFDA (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

• 4/5SevereFDA (Drugs)·D-0524-2026·2026-05-13

  TPN Bag Recalled for Missing Insulin Formulation Error

  Central Admixture Pharmacy Services is recalling a patient-specific TPN bag because it did not contain insulin as listed on the label. Patients relying on this product for the labeled insulin dosage may face serious health risks.

  Product

  TPN bag (patient specific), Rx# 11-4909703-0-1, Compound Volume 1660 mL per bag, Rx only, Single Dose Injection, Refrigerated Injection, Central Admixture Pharmacy Services, Los Angeles, 13128 Imperial Hwy, Santa Fe Spr., CA 90670

  Category

  Drug

  Distribution

  1 state

• 4/5SevereFDA (Food)·H-0700-2026·2026-05-13

  Buttermilk Powder Recalled Due to Potential Salmonella Contamination

  California Dairies Inc. is recalling buttermilk powder in 25 kg paper bags due to potential Salmonella contamination. The product was distributed domestically and to Mexico, the Philippines, and the Dominican Republic.

  Product

  Buttermilk Powder - paper bags 25 kg. (packed under 1 label: BMP Extra Grade Standard)

  Category

  Food

  Distribution

  0 states

• 4/5SevereFDA (Devices)·Z-1979-2026·2026-05-13

  Halyard VA Detroit Cath Lab Pack Kit Syringe Adaptor Disconnection Risk

  Halyard VA Detroit Cath Lab Pack kits (Model VMCD029) are being recalled due to a potential risk that the Medline syringe rotating adaptor may unwind during use, causing a loose or full disconnection between the syringe and manifold.

  Product

  Halyard VA DETROIT CATH LAB PACK kit. Model Numbers: VMCD029.

  Category

  Medical Device

  Distribution

  7 states

• 4/5SevereFDA (Drugs)·D-0517-2026·2026-05-13

  PurPrep Povidone-Iodine and Isopropyl Alcohol Solution Recalled for Sterility Assurance

  CareFusion 213, LLC is recalling PurPrep sterile topical solution due to lack of assurance of sterility and potential product contamination. The affected product is a povidone-iodine and isopropyl alcohol solution distributed nationwide.

  Product

  PURPREP — PURPREP (POVIDONE IODINE AND ISOPROPYL ALCOHOL)

  Category

  Drug

  Distribution

  Distributed nationwide

• 4/5SevereFDA (Devices)·Z-1855-2026·2026-05-13

  Intuitive 8 mm SureForm 30 Gray Reloads Incomplete Staple Defect

  Intuitive Surgical is recalling Intuitive 8 mm SureForm 30 Gray Reloads (Reference Numbers 48230M-05 and 48230M-06) because they may produce an incomplete staple line during curved-tipped stapler operations.

  Product

  Intuitive 8 mm SureForm 30 Gray Reloads Reference Numbers: 48230M-05 and 48230M-06

  Category

  Medical Device

  Distribution

  0 states

• 4/5SevereFDA (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

• 4/5SevereFDA (Devices)·Z-1970-2026·2026-05-13

  Halyard Cardiac Cath Pack Kit Syringe Adapter Unwinding Risk

  AVID Medical recalls Halyard Cardiac Cath Pack kits (Models EAMC1000-05, WAFB208-02) due to risk that a Medline syringe rotating adapter may unwind during use, causing loose or full disconnection between the syringe and manifold.

  Product

  Halyard CARDIAC CATH PACK kit. Model Number: EAMC1000-05, WAFB208-02.

  Category

  Medical Device

  Distribution

  7 states

• 4/5SevereFDA (Devices)·Z-1975-2026·2026-05-13

  Halyard HEART CATH SELF REGIONAL kit syringe adapter disconnection hazard

  AVID Medical is recalling the Halyard HEART CATH SELF REGIONAL kit (Model SELF131-05) because the Medline syringe rotating adaptor may unwind during use, causing a loose or full disconnection between the syringe and manifold.

  Product

  Halyard HEART CATH, SELF REGIONAL kit. Model Number: SELF131-05.

  Category

  Medical Device

  Distribution

  7 states

• 4/5SevereFDA (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

• 4/5SevereFDA (Food)·H-0691-2026·2026-05-13

  Costco Service Deli Meatloaf Seasoning Recalled for Potential Salmonella

  Griffith Foods is recalling Costco Service Deli meatloaf seasoning because the nonfat dry milk ingredient may be contaminated with Salmonella. The product was distributed to Costco locations in 15 states.

  Product

  Costco Service Deli Department 63 MEATLOAF SEASONING MORE FLV Pack Size: 4-5lb. Bags Net Weight: 20lbs Allergy Information: CONTAINS: MILK, WHEAT Packed BY: Griffith Foods STONECREST, GA 30058

  Category

  Food

  Distribution

  15 states

• 4/5SevereFDA (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

• 4/5SevereFDA (Devices)·Z-2062-2026·2026-05-13

  ERBEFLO CleverCap CO2 Tubing and Cap Sets for Endoscopes

  Erbe Medical is recalling ERBEFLO CleverCap CO2 hybrid tubing and cap sets used with endoscopes because the distal connector may allow unintended water flow, potentially leading to water aspiration and serious respiratory complications.

  Product

  ERBEFLO CleverCap CO2: Hybrid CO2 Tubing/Cap Set for Olympus Scopes & CO2 Sources, REF: 20325-239; Hybrid CO2 Tubing/Cap Set for Olympus Scopes & UCR, REF: 20325-240; Hybrid CO2 Tubing/Cap Set for Olympus Scopes, REF: 20325-206; Hybrid CO2 Tubing/Cap Set for Pentax Scopes, REF: 2

  Category

  Medical Device

  Distribution

  Distributed nationwide

• 4/5SevereFDA (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

• 4/5SevereFDA (Devices)·Z-1971-2026·2026-05-13

  Halyard CARDIAC CATH PACK SAN23CARDQ Kit Syringe Adapter Risk

  AVID Medical is recalling Halyard CARDIAC CATH PACK SAN23CARDQ kits (Model DRCC36) due to a Medline syringe rotating adapter that may unwind during use, potentially causing loose or full disconnection between the syringe and manifold.

  Product

  Halyard CARDIAC CATH PACK SAN23CARDQ kit. Model Number: DRCC36.

  Category

  Medical Device

  Distribution

  7 states

• 4/5SevereFDA (Devices)·Z-1973-2026·2026-05-13

  Halyard CATH LAB Kit Recalled for Syringe Adapter Disconnection Risk

  AVID Medical is recalling the Halyard CATH LAB kit (Model SACL75AM) because the syringe rotating adapter may unwind during use, causing a loose or full disconnection between the syringe and manifold.

  Product

  Halyard CATH LAB kit. Model Number: SACL75AM.

  Category

  Medical Device

  Distribution

  7 states

• 4/5SevereFDA (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

• 4/5SevereFDA (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

• 4/5SevereFDA (Devices)·Z-1942-2026·2026-05-13

  VOCSN V+Pro Ventilator System Respiratory Device Safety Recall

  Ventec Life Systems is recalling VOCSN V+Pro ventilator units because they may not have been fully tested for high-pressure conditions, which could cause oxygen leaks and increase fire risk during use.

  Product

  VOCSN V+Pro package, REF: PRT-01198-000; VOCSN V+Pro unit, REF: PRT-01185-000

  Category

  Medical Device

  Distribution

  4 states

• 4/5SevereFDA (Food)·H-0698-2026·2026-05-13

  Low Heat Non-Fat Dried Milk Powder Recalled for Salmonella Risk

  California Dairies Inc. is recalling Low Heat Non-Fat Dried Milk Powder due to potential Salmonella contamination. The recall affects approximately 1.11 million pounds distributed across the United States, Mexico, Philippines, and Dominican Republic.

  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

• 4/5SevereFDA (Devices)·Z-2007-2026·2026-05-13

  Medical Action Industries Pack Cath BHH Catheter Kit Recall

  Medical Action Industries is recalling Pack Cath BHH catheter kits because the rotating adapter may unwind during use, causing a loose or full disconnection between the syringe and manifold.

  Product

  Medical Action Industries Inc. Pack Cath BHH, REF: BHCA49K, Sterile EO, Rx Only, QTY: 5/Case

  Category

  Medical Device

  Distribution

  1 state

• 4/5SevereFDA (Food)·H-0766-2026·2026-05-13

  Raw Farm Original Raw Cheddar Cheese Recalled for E. coli O157

  Raw Farm LLC is recalling Raw Farm Original Raw Cheddar 80 oz bulk cheese due to a multi-state outbreak of E. coli O157:H7.

  Product

  RAW FARM ORIGINAL RAW CHEDDAR 80 OZ [BULK ITEM] UPC: 835204001160

  Category

  Food

  Distribution

  10 states

• 4/5SevereFDA (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

• 4/5SevereFDA (Devices)·Z-1972-2026·2026-05-13

  Halyard Cardiac Catheterization Tray Kits Recalled for Connection Risk

  AVID Medical is recalling Halyard CARDIAC CATH TRAY SHANDS JAX kits due to a defect in the Medline syringe rotating adaptor that may unwind during use, causing a loose or full disconnection between the syringe and manifold.

  Product

  Halyard CARDIAC CATH TRAY SHANDS JAX kit. Model Number: SHND401-04, SHND401-05.

  Category

  Medical Device

  Distribution

  7 states