Recalls published in November 2025
Everything the FDA, USDA FSIS, CPSC and NHTSA announced in November 2025, newest first.
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Highest risk · 12 months ago
Sanven Technology Vevor Baby Swings recall: Risk of Serious Injury from Suffocation Hazard
Risk of Serious Injury from Suffocation Hazard; Violates Mandatory Standard for Infant Sleep Products and Inclined Sleepers Ban
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Elevated risk · 12 months ago
Peloton Original Series Bike+ Exercise Bikes recall: Fall and Injury Hazards
Fall and Injury Hazards
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Highest risk · 12 months ago
Napei Collapsible Infant Bath Tubs recall: The recalled infant bath tubs violate the mandatory standard for consumer
The recalled infant bath tubs violate the mandatory standard for consumer products containing button cell or coin batteries because the built-in…
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Highest risk · 12 months ago
Lezyne USA Bicycle Floor Pumps recall: Serious Injury Hazard
Serious Injury Hazard
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Highest risk · 12 months ago
Inkari Plush Alpaca Toys recall: The recalled toys are intended for children under three years of age
The recalled toys are intended for children under three years of age and the eyes can detach, which violates the small parts ban, posing a choking…
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Highest risk · 12 months ago
F&F Fine Wines Kirkland Signature Valdobbiadene Prosecco Entrapment or Suffocation recall: Risk of Serious Injury or Death from Entrapment
Risk of Serious Injury or Death from Entrapment
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Highest risk · 12 months ago
F&F Fine Wines Kirkland Signature Valdobbiadene Prosecco DOCG Bottles sold by Costco recall: Laceration Hazard
Laceration Hazard
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Highest risk · 12 months ago
Astemrey Y'all Can DIY Liquid Bioethanol Fireplace Fuel Containers recall: Risk of Serious Injury or Death from Flash Fire
Risk of Serious Injury or Death from Flash Fire; Violates Mandatory Standard for Portable Fuel Containers
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Highest risk · 12 months ago
Neaude Adult Portable Bed Rails recall: The recalled bed rails violate the mandatory standard for adult portable bed
The recalled bed rails violate the mandatory standard for adult portable bed rails, posing a serious entrapment hazard and risk of death by…
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Class II · 12 months ago
CareFusion 303, Inc. Various models of BD Pyxis Medbank: Reference numbers: 1137-00 recall: Potential fluid ingress of anesthesia station or med station may result
Potential fluid ingress of anesthesia station or med station may result in smoke, system downtime and/or fire.
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Class II · 12 months ago
CareFusion 303, Inc. All Serial Numbers/BD Pyxis CII Safe ES Tower Main, REF: 1116-00 recall: Potential fluid ingress of anesthesia station or med station may result
Potential fluid ingress of anesthesia station or med station may result in smoke, system downtime and/or fire.
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Class II · 12 months ago
Brand Name: Alcon Laboratories, Inc. Product Name: Accessory devices recall: Due to incomplete seals in the pouch which provide the sterile barrier
Due to incomplete seals in the pouch which provide the sterile barrier.
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Class II · 12 months ago
Daye Refill 18 Coated Regular and 18 Coated Super Tampons recall: Product lacks 510(k) clearance
Product lacks 510(k) clearance.
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Class II · 12 months ago
Daye 9 Coated Regular Tampons and 9 Nude Regular Tampons recall: Product lacks 510(k) clearance
Product lacks 510(k) clearance.
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Class II · 12 months ago
Daye Initiation 18 Coated Super and 18 Nude Super Tampons recall: Product lacks 510(k) clearance
Product lacks 510(k) clearance.
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Class II · 12 months ago
Brand Name: Aesculap Product Name: Sealing Unit FOR 10/12MM Trocars recall: It was determined there is the potential of silicone fragments detaching
It was determined there is the potential of silicone fragments detaching from the yellow sealing component.
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Class II · 12 months ago
Brand Name: Aesculap Product Name: Sealing CAP FOR 10/12MM Trocars recall: It was determined there is the potential of silicone fragments detaching
It was determined there is the potential of silicone fragments detaching from the yellow sealing component.
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Class II · 12 months ago
Daye 9 Coated Regular and 9 Coated Super Tampons recall: Product lacks 510(k) clearance
Product lacks 510(k) clearance.
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Class II · 12 months ago
Daye All in One Bundle recall: Product lacks 510(k) clearance
Product lacks 510(k) clearance.
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Class II · 12 months ago
ICU Medical ChemoLock Universal Vented Vial Spike REF: CL-70 recall: Port weld of drug transfer device may separate or break during use
Port weld of drug transfer device may separate or break during use and potentially result in a leak.
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Class II · 12 months ago
Endomagnetics Ltd Magseed Pro 7 cm soft tissue marker recall: Potential for contamination with cotton fibers
Potential for contamination with cotton fibers.
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Class II · 12 months ago
ICU Medical ChemoLock Vented Vial Spike, 13mm REF: CL-72 recall: Port weld of drug transfer device may separate or break during use
Port weld of drug transfer device may separate or break during use and potentially result in a leak.
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Class II · 12 months ago
ICU Medical 60" Appx 1.2 ml, Ext Set, Smallbore w/ChemoLock Port recall: Port weld of drug transfer device may separate or break during use
Port weld of drug transfer device may separate or break during use and potentially result in a leak.
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Class I · 12 months ago
IMPRIS Imaging Inc IMRIS Operating Suite, iMRI 3T S, containing Siemens 3 Tesla MRI recall: There is a potential safety issue associated with the magnet venting paths
There is a potential safety issue associated with the magnet venting paths of the Siemens 3 Tesla MRI system within your IMRIS Operating Suite…