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Consumer Product Recalls
127,244 recalls from the U.S. Consumer Product Safety Commission, newest first.
May 13, 2026Medical DevicesFDA
Intuitive Surgical, Inc. recalls Brand Name: Da Vinci X and Da Vinci Xi Product Name: da Vinci X, Xi Surgical System Model/Catalog Number: IS4000; IS4
Hazard: Due to manipulator containing screws with in the arm sub-assembly that my be susceptible to breaking.
May 13, 2026Medical DevicesFDA
Medical Action Industries, Inc. 306 recalls Medical Action Industries Inc. Pack Cath BHH, REF: BHCA49K, Sterile EO, Rx Only, QTY: 5/Case
Hazard: Convenience kit contains a syringe in which the rotating adapter may unwind during use, resulting in a loose connection and/or full disconnection between the syringe and manifold"
May 13, 2026Medical DevicesFDA
American Contract Systems Inc recalls Convenience kits containing Medline Namic Angiographic Control Syringes with Rotating Adaptor CORONARY ANGIO PACK Mo
Hazard: Impacted kits contain syringes recalled by Medline Industries. Syringe rotating adaptor may unwind during use, which may result in a loose connection or full disconnection between the syringe and manifold. Potential risk for biohazard exposure, blood loss, infection, or air embolism.
May 13, 2026Medical DevicesFDA
AVID Medical, Inc. recalls Halyard VA DETROIT CATH LAB PACK kit. Model Numbers: VMCD029.
Hazard: Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
May 13, 2026Medical DevicesFDA
AVID Medical, Inc. recalls Halyard SAMMC ANGIOGRAPHY kit. Model Numbers: SAMM066-15.
Hazard: Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
May 13, 2026Medical DevicesFDA
AVID Medical, Inc. recalls Halyard PERC TRAY kit. Model Numbers: SLPC34-01, SLPC34-02.
Hazard: Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
May 13, 2026Medical DevicesFDA
AVID Medical, Inc. recalls Halyard NEURO IR PERIPHERAL (PS 64405) kit. Model Number: UINR44-01.
Hazard: Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
May 13, 2026Medical DevicesFDA
AVID Medical, Inc. recalls Halyard HEART CATH, SELF REGIONAL kit. Model Number: SELF131-05.
Hazard: Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
May 13, 2026Medical DevicesFDA
AVID Medical, Inc. recalls Halyard CATH LAB kit. Model Number: SACL75-01.
Hazard: Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
May 13, 2026Medical DevicesFDA
AVID Medical, Inc. recalls Halyard CATH LAB kit. Model Number: SACL75AM.
Hazard: Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
May 13, 2026Medical DevicesFDA
AVID Medical, Inc. recalls Halyard CARDIAC CATH TRAY SHANDS JAX kit. Model Number: SHND401-04, SHND401-05.
Hazard: Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
May 13, 2026Medical DevicesFDA
AVID Medical, Inc. recalls Halyard CARDIAC CATH PACK SAN23CARDQ kit. Model Number: DRCC36.
Hazard: Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
May 13, 2026Medical DevicesFDA
AVID Medical, Inc. recalls Halyard CARDIAC CATH PACK kit. Model Number: EAMC1000-05, WAFB208-02.
Hazard: Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
May 13, 2026Medical DevicesFDA
Ventec Life Systems, Inc. recalls VOCSN V+Pro package, REF: PRT-01198-000; VOCSN V+Pro unit, REF: PRT-01185-000
Hazard: Respiratory system intended to provide continuous/intermittent ventilator support, may not have been evaluated under all intended high-pressure conditions during production testing, so an oxygen leak condition could occur that may lead to reduced below intended levels of fraction of inspired oxygen delivery prior to and during ventilation and this oxygen-enriched environment may increase fire risk
May 13, 2026Medical DevicesFDA
Cook Incorporated recalls 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
Hazard: Marker bands may be at an increased risk of cracking/breakage. Potential adverse events that may result include increased procedural time, harms associated with device fragmentation/separation, and vessel injury. In a worst-case scenario, device fragmentation and separation may cause life-threatening harm or death.
May 13, 2026Medical DevicesFDA
Cook Incorporated recalls Aurous Centimeter Sizing Catheter RPN N5.0-35-100-P-10S-PIG-CSC-20-01 GPN G47308 Sizing catheters are single-use, s
Hazard: Marker bands may be at an increased risk of cracking/breakage. Potential adverse events that may result include increased procedural time, harms associated with device fragmentation/separation, and vessel injury. In a worst-case scenario, device fragmentation and separation may cause life-threatening harm or death.
May 13, 2026Medical DevicesFDA
Cook Incorporated recalls Centimeter Sizing Catheter RPN N5.0-35-100-P-10S-PIG-CSC-20 GPN G11916 Catheters for use in angiographic procedures
Hazard: Marker bands may be at an increased risk of cracking/breakage. Potential adverse events that may result include increased procedural time, harms associated with device fragmentation/separation, and vessel injury. In a worst-case scenario, device fragmentation and separation may cause life-threatening harm or death.
May 13, 2026Medical DevicesFDA
Intuitive Surgical, Inc. recalls Intuitive 8 mm SureForm 30 Gray Reloads Reference Numbers: 48230M-05 and 48230M-06
Hazard: Reloads for curved-tipped stapler may potentially produce an incomplete staple line.
May 13, 2026Food & BeverageFDA
Givaudan Flavors Corp recalls Bulk WN-976-782-1 Seasoning for Cheese Sauce, Net Wt. 43.50 lbs., in a brown kraft bag
Hazard: Product has the potential to be contaminated with Salmonella.
May 13, 2026Food & BeverageFDA
Post Consumer Brands, LLC recalls Publix Bran Flakes, Wheat Cereal. Net Wt 18oz (1 lb 2 oz) 510g. UPC 0 41415-24305 7. Distributed by Publix Super Mar
Hazard: Foreign Material (plastic)
May 13, 2026Food & BeverageFDA
Wehah Farms recalls LUNDBERG FAMILY FAMRS WHITE RICE JASMINE NET WT 32 OZ (2 lb) 907 g Manufactured and Distributed by: Lundberg Family Far
Hazard: Potential contamination with foreign materials.
May 13, 2026Food & BeverageFDA
Raw Farm LLC recalls RAW FARM ORIGINAL RAW CHEDDAR 80 OZ [BULK ITEM] UPC: 835204001160
Hazard: Multi-state outbreak of E. coli O157:H7.
May 13, 2026Food & BeverageFDA
Raw Farm LLC recalls RAW FARM SHREDDED RAW CHEDDAR 80 OZ [BULK ITEM] UPC: 835204000194
Hazard: Multi-state outbreak of E. coli O157:H7.
May 13, 2026Food & BeverageFDA
Raw Farm LLC recalls RAW FARM RAW CHEDDAR SIMPLY SHREDDED Original MADE WITH: WHOLE RAW MILK TRULY RAW - NEVER WARMED ABOVE 102F MADE IN THE
Hazard: Multi-state outbreak of E. coli O157:H7.
May 13, 2026Food & BeverageFDA
Raw Farm LLC recalls RAW FARM RAW CHEDDAR Jalapeno NEVER WARMED ABOVE 102F (TRULY RAW) MADE WITH WHOLE RAW MILK MADE IN USA KEEP REFRIGERATED
Hazard: Multi-state outbreak of E. coli O157:H7.
May 13, 2026Food & BeverageFDA
Raw Farm LLC recalls RAW FARM RAW CHEDDAR Original NEVER WARMED ABOVE 102F (TRULY RAW) MADE WITH WHOLE RAW MILK MADE IN USA KEEP REFRIGERATED
Hazard: Multi-state outbreak of E. coli O157:H7.
May 13, 2026Food & BeverageFDA
Target Corporation recalls Good & Gather Fresh from Our Deli. Sesame Teriyaki Chicken with Rice. Net Wt 18.0 oz (1.125lb). Keep Refrigerated. D
Hazard: Undeclared allergens (sesame and soy)
May 13, 2026Food & BeverageFDA
Silver Moon LP dba Loard's Ice Cream recalls Chocolate Showers Ice Cream - 32 oz (5 labels: Mollie Stone's; Dehoff's; Farmer Joe's, Piazza's Fine Foods, and Berkeley
Hazard: Undeclared Soy (with mitigating circumstances)
May 13, 2026Food & BeverageFDA
Silver Moon LP dba Loard's Ice Cream recalls Peppermint Ice Cream - 32 oz (4 labels: Mollie Stone's; Dehoff's; Farmer Joe's, Piazza's Fine Foods) UPC: 8-12017-00933
Hazard: Undeclared Red #40
May 13, 2026Food & BeverageFDA
Silver Moon LP dba Loard's Ice Cream recalls Chocolate Mint Ice Cream - 32 oz (4 labels: Mollie Stone's; Dehoff's; Farmer Joe's, Piazza's Fine Foods) UPC: 8-12017-00
Hazard: Undeclared Soy (with mitigating circumstances), Yellow #5, Blue #1