Acecide-C Acecide-C (PLAC01)Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10359900300008), received between Nov 27, 2024 and Nov 27, 2024 — classified as 1 injury.

The most frequently reported specific device problem is “Explosion” (1 report).

1 other recall cover devices cleared under the same FDA submission (K091210); they may or may not involve this specific model.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.

Most reported problems

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• InjuryNov 27, 2024Explosion; Explosion

  THE STAFF WAS CHANGING THE LIQUID CHEMICALS IN THE OER-PRO MACHINE. THE BOTTOM OF THE BOTTLE WOULD NOT FIT INTO THE TRAY. THE STAFF MEMBER TOOK A SYRINGE AND PUNCTURED THE BOTTLE TO RELIEVE PRESSURE AND CAUSE THE BOTTLE TO DEFLATE. THE BOTTLE "EXPLODED" ONTO THE FACE AND ARMS OF THE STAFF MEMBER. THE STAFF WAS NOT WEARING PPE AND SUSTAINED A CHEMICAL BURN. USED THE EYEWASH STATION FOR TEN MINUTES AND YES EYES WERE STILL IRRITATED AND SAW WHITE SPOTS. THE STAFF MEMBER WAS TREATED AT THE HOSPITAL THE DAY OF THE EVENT AND HAVE HAD SEVERAL TRIPS TO THE EYE DOCTOR. NO SUSTAINED DAMAGE.

  Patient problems: Caustic/Chemical Burns; Eye Burn

  MAUDE report 20802566 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K091210. One submission often covers many models, so check the product and lot details in each record.

• Z-2714-2016 · Aug 2, 2016 · Terminated
  Acecide-C High Level Disinfectant & Sterilant 875 mL. Packaging is 6 inner cartons in one master carton;1 inner carton consists of a set of two liquids (1 acid & 1 buffer) banded