FDAJune 22, 2018device
Aplicare Povidone Iodine Prep Pads packaged within Portex Pulsator Arterial Blood Sampling Kit with Liquid Sodium Heparin, models 4037NP-1, 4039-1, 4039EG-1, 4044EG-1, 4044P-1, 4057NP-1, 4067NP-1, 4077EG-1, 4077NP-1, 4084P-1, G1193, G1374, G1585, G1589, G1598, G1621, and G1806. The firm name on t...
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
The povidone iodine prep pads packaged with the arterial blood sampling kits will not maintain the iodine potency through its labeled 36-month expiration dating.
What to do
FDA enforcement status: Terminated
Brands named
smiths medical asdsmithssmiths medical
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
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