Overview of recall records associated with Cardinal Health 200, LLC, including dates, categories and classifications where available.
Classification mix: Class II: 208, Class I: 28.
Labeling issue in that the breakthrough (i.e., permeation) times for two chemotherapy drugs (Carmustine and Thiotepa) stated on the wallet (primary packaging) of the Protexis Neoprene…
Labeling issue in that the breakthrough (i.e., permeation) times for two chemotherapy drugs (Carmustine and Thiotepa) stated on the wallet (primary packaging) of the Protexis Neoprene…
Labeling issue in that the breakthrough (i.e., permeation) times for two chemotherapy drugs (Carmustine and Thiotepa) stated on the wallet (primary packaging) of the Protexis Neoprene…
Labeling issue in that the breakthrough (i.e., permeation) times for two chemotherapy drugs (Carmustine and Thiotepa) stated on the wallet (primary packaging) of the Protexis Neoprene…
The suction valve may not close properly which could cause continuous suction.
The suction valve may not close properly which could cause continuous suction.
The suction valve may not close properly which could cause continuous suction.
The suction valve may not close properly which could cause continuous suction.
The suction valve may not close properly which could cause continuous suction.
The suction valve may not close properly which could cause continuous suction.
A defect in the seal of the Gatorade pouch contained in kits caused the pouch to leak within a limited portion of the kit.
The suction valve may not close properly which could cause continuous suction.
The suction valve may not close properly which could cause continuous suction.
A defect in the seal of the Gatorade pouch contained in kits caused the pouch to leak within a limited portion of the kit.
The suction valve may not close properly which could cause continuous suction.
The suction valve may not close properly which could cause continuous suction.
A defect in the seal of the Gatorade pouch contained in kits caused the pouch to leak within a limited portion of the kit.
A defect in the seal of the Gatorade pouch contained in kits caused the pouch to leak within a limited portion of the kit.
The suction valve may not close properly which could cause continuous suction.
products may be missing a one-way valve on the fluid patient port.
This page summarizes recall records in which the official source identifies Cardinal Health 200, LLC as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.
