2,756 recalls tagged with “immediate action”.
This recall involves Evermore Surprise Eggs with yellow, pink or green wrap. The Surprise Eggs are gold and contain seven different toys including a toy airplane.
This recall involves Almpal dissolved oxygen test kits. The test kits come in a cream-colored box bearing a white label with "Dissolved Oxygen Test Kit" and the manufacture date, batch number, and expiration date printed on it.
Possible stainless steel pieces in product.
ICU Medical recalls 23,203 IV gravity burette sets worldwide. The burette component is missing an internal shutoff valve, which can delay therapy, cause overdelivery, or allow air to be infused. Stop using the device and contact ICU Medical for instructions.
Potential contamination with foreign objects.
Potential cybersecurity vulnerabilities related to the operating system in the Automated Impella Controller (AIC).
Labeling: Label Mix-up: The product in the bottle contains elderberry and the label failed to indicate the inclusion of elderberry as an ingredient.
Presence of Particulate Matter: Particulate matter identified as glass
Contains Linguine manufactured by Nate's Fine Foods LLC recalled for Listeria monocytogenes and implicated in ongoing outbreak
The potential contamination with Clostridium botulinum, due to risk of temperature abuse during chilled storage at the firm.
The potential for micro-air bubbles observed in the bloodline and air-in-line alarms due to damaged arterial and venous patient connectors.
Lack of Remote Interlock Connector - required per 21 CFR 1040.10(f)(3)
cGMP deviations: The recall was initiated because required receipt testing of incoming alcohol components used to manufacture the listed hand sanitizers was not performed, so methanol risk could not be excluded.
Product may be contaminated with Listeria monocytogenes.
Over time some systems may experience loss of imaging functionality and/or poor image quality due to potential corrosion of the Image Intensifier Television (IITV) control board.
Medline Industries recalled 222,800 alcohol prep pads nationwide on Sept. 29, 2025 due to subpotent potency. The pads are 2-ply, 70% isopropyl alcohol. Stop using immediately and contact Medline or your healthcare provider for guidance.
cGMP deviations: The recall was initiated because required receipt testing of incoming alcohol components used to manufacture the listed hand sanitizers was not performed, so methanol risk could not be excluded.
Failed dissolution specifications: Stability testing found that the lot did not meet dissolution specifications.
Fish is un-eviscerated (may be contaminated with Clostridia botulinum), is contaminated with mold, and contains filth (insect larvae)