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All product recalls associated with ALTEC.
Total Recalls
1000
Past Year
1000
Class I (Serious)
145
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.
Altec Industries Inc. (Altec) is recalling certain 2025 AP Series vehicles. The brake air line compression fitting may not be tightened correctly, which can allow the supply line or other air lines to detach and cause the chassis emergency brakes to engage.
Baxter Healthcare Corporation is issuing an Urgent Medical Device Recall for one lot of Continu-Flo solution sets listed below due to customer reports of tubing separation.
Software issue that results in the display of outdated information.
Flowmeter patch as a human readable expiry date on the outer shipping packaging that reads 2025-06-20 when it should read 2026-06-20.
This recall involves Séfralls Hair Generation Serum. The hair serum comes in an amber dropper bottle with a white and gold dropper and a white, black and gold label. "Séfralls" and "Minoxidil" are printed on the label located on the front of the bottle.
Product may contain small metal fragments due to contaminated onion powder ingredient used in manufacturing.
Product may contain small metal fragments due to contaminated onion powder ingredient used in manufacturing.
Product may contain small metal fragments due to contaminated onion powder ingredient used in manufacturing.
Product may contain small metal fragments due to contaminated onion powder ingredient used in manufacturing.
Potential for undetected, deformed a-traumatic tips.
Fontaine Modification Company (Fontaine Modification) is recalling certain 2022-2024 Freightliner Business Class M2 vehicles. Welds may crack and fail, allowing the Intermediate steering shaft assembly to detach from the steering column.
The catheters may not retain their shape.
Unapproved Drug Claims and Misbranded.
Allergen labeling: specific tree nut (pecan) and egg not listed in 'contains' statement
Unapproved Drug Claims.
Unapproved Drug Claims.
Unapproved Drug Claims and Misbranded.
Unapproved Drug Claims.
CGMP Deviations: Presence of a nitrosamine, N-nitroso-metoprolol above the established Acceptable Daily Intake (ADI) level.
CGMP Deviations: Presence of a nitrosamine, N-nitroso-metoprolol above the established Acceptable Daily Intake (ADI) level.