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All product recalls associated with ICU Medical, Inc..
Total Recalls
1000
Past Year
1000
Class I (Serious)
34
Most Recent
Jan 2026
Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.
Due to a manufacturing defect which results in a visible gap between the connector's top and bottom housing.
Due to a manufacturing defect which results in a visible gap between the connector's top and bottom housing.
Device label display an incorrect expiration date, extends the shelf life of the product. Affected product distributed in the United States from 3/25/2018 to 9/28/2020, expiration dates between 2022-11-01 and 2025-09-01 (Devices have a lot number ending in R, or are kits containing at least 1 device with a lot number ending in R.)
Device label display an incorrect expiration date, extends the shelf life of the product. Affected product distributed in the United States from 3/25/2018 to 9/28/2020, expiration dates between 2022-11-01 and 2025-09-01 (Devices have a lot number ending in R, or are kits containing at least 1 device with a lot number ending in R.)
Device label display an incorrect expiration date, extends the shelf life of the product. Affected product distributed in the United States from 3/25/2018 to 9/28/2020, expiration dates between 2022-11-01 and 2025-09-01 (Devices have a lot number ending in R, or are kits containing at least 1 device with a lot number ending in R.)
Device label display an incorrect expiration date, extends the shelf life of the product. Affected product distributed in the United States from 3/25/2018 to 9/28/2020, expiration dates between 2022-11-01 and 2025-09-01 (Devices have a lot number ending in R, or are kits containing at least 1 device with a lot number ending in R.)
Device label display an incorrect expiration date, extends the shelf life of the product. Affected product distributed in the United States from 3/25/2018 to 9/28/2020, expiration dates between 2022-11-01 and 2025-09-01 (Devices have a lot number ending in R, or are kits containing at least 1 device with a lot number ending in R.)
Device label display an incorrect expiration date, extends the shelf life of the product. Affected product distributed in the United States from 3/25/2018 to 9/28/2020, expiration dates between 2022-11-01 and 2025-09-01 (Devices have a lot number ending in R, or are kits containing at least 1 device with a lot number ending in R.)
Device label display an incorrect expiration date, extends the shelf life of the product. Affected product distributed in the United States from 3/25/2018 to 9/28/2020, expiration dates between 2022-11-01 and 2025-09-01 (Devices have a lot number ending in R, or are kits containing at least 1 device with a lot number ending in R.)
Device label display an incorrect expiration date, extends the shelf life of the product. Affected product distributed in the United States from 3/25/2018 to 9/28/2020, expiration dates between 2022-11-01 and 2025-09-01 (Devices have a lot number ending in R, or are kits containing at least 1 device with a lot number ending in R.)
Device label display an incorrect expiration date, extends the shelf life of the product. Affected product distributed in the United States from 3/25/2018 to 9/28/2020, expiration dates between 2022-11-01 and 2025-09-01 (Devices have a lot number ending in R, or are kits containing at least 1 device with a lot number ending in R.)
Device label display an incorrect expiration date, extends the shelf life of the product. Affected product distributed in the United States from 3/25/2018 to 9/28/2020, expiration dates between 2022-11-01 and 2025-09-01 (Devices have a lot number ending in R, or are kits containing at least 1 device with a lot number ending in R.)
Device label display an incorrect expiration date, extends the shelf life of the product. Affected product distributed in the United States from 3/25/2018 to 9/28/2020, expiration dates between 2022-11-01 and 2025-09-01 (Devices have a lot number ending in R, or are kits containing at least 1 device with a lot number ending in R.)
Device label display an incorrect expiration date, extends the shelf life of the product. Affected product distributed in the United States from 3/25/2018 to 9/28/2020, expiration dates between 2022-11-01 and 2025-09-01 (Devices have a lot number ending in R, or are kits containing at least 1 device with a lot number ending in R.)
This recall involves model year 2022 Arctic Cat Alterra 600 and model year 2022 Tracker 600 All-Terrain Vehicles (ATVs). The Arctic Cat Alterra 600 ATVs were sold in various colors, including green, gray and fossil (tan). The Tracker 600 vehicles were sold in various colors, including red, white, STRATA Camo and gray. The Vehicle Identification Number (VIN) is located on the front right-hand frame tube beside the right-hand shock. The VIN number ranges for recalled Arctic Cat Alterra 600 and Tracker 600 include the following: MY Model VIN Start VIN End 2022 Arctic Cat Alterra 600 NT200101 NT201133 2022 Tracker 600 NT200101 NT201363
This recall involves Aesop Post-Poo Drops, a bathroom deodorizer in a 100 mL amber glass bottle, with a continuous thread pipette dispenser closure. The bottle has a black and cream label with the brand name Aesop. The UPC number 9319944009200 is located on the rear of the bottle, directly below the ingredients list. The deodorizer product was also sold in four versions of the Home Kit: The Protector, The Seasoned Wayfarer, The Melodist, and The Familiar Horizon. The UPC numbers for four versions of the Home Kit are located on the rear of the printed sleeve. Only the Aesop Post-Poo Drops in the kit are included in this recall. The product names and UPC are as follows: Product Name UPC Description Post-Poo Drops 9319944009200 100 mL amber glass bottle, with a continuous thread pipette dispenser closure The Protector 9319944030198 100 mL amber glass bottle, with a continuous thread pipette dispenser closure The Seasoned Wayfarer 9319944023794 100 mL amber glass bottle, with a continuous thread pipette dispenser closure The Melodist 9319944022278 100 mL amber glass bottle, with a continuous thread pipette dispenser closure The Familiar Horizon 9319944016017 100 mL amber glass bottle, with a continuous thread pipette dispenser closure. This recall also involves four Aesop Oil Burner Blends: Anouk, Beatrice, Catherine, and Isabelle. The aromatic oil blends intended to be used in an oil burner. These products include a black and cream label with the brand name Aesop and the blend name. They come in a 25 mL amber glass bottle with a continuous thread closure and flow restrictor insert. The UPC numbers for the Oil Burner Blends are located on the rear of each bottle, below the ingredients lists. The product names and UPC for the recalled Oil Burner Blend products are as follows: Product Name UPC Description Anouk Oil Burner Blend 9319944000696 25 mL amber glass bottle with a continuous thread closure and flow restrictor insert Beatrice Oil Burner Blend 9319944000702 25 mL amber glass bottle with a continuous thread closure and flow restrictor insert Catherine Oil Burner Blend 9319944000689 25 mL amber glass bottle with a continuous thread closure and flow restrictor insert Isabelle Oil Burner Blend 9319944016871 25 mL amber glass bottle with a continuous thread closure and flow restrictor insert
CGMP Deviations:OOS result was observed in 1-Methyl-4-Nitroso Piperazine (MNP) impurity.
An incorrect sizing label was applied to the carton packaging.
Corp. Micro Bird, Inc. (Micro Bird) is recalling certain 2021-2022 G5, MBII, and T-Series school buses. The inside panels under the windows may have been insufficiently attached. As such, these vehicles fail to comply with the requirements of the Federal Motor Vehicle Safety Standard number 221, "School Bus Body Joint Strength."
(1)Software version 2.74 upgrade and (2)hardware related cause that affects only CDX Machines, has been identified as the UI-MICs Board is sensitive to Electromagnetic Interference (EMI) which will cause the false alarm "Remove USB 2 Device".