Apollo Corp. WP6300Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00866595000203), received between Nov 13, 2017 and Nov 13, 2017 — classified as 1 injury.

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

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 13, 2017Material Separation

  THE INCIDENT OCCURRED AS THE CARETAKER WAS REMOVING THE RESIDENT FROM THE BATHING SYSTEM. THE CARETAKER ROLLED THE CHAIR (UPPER TRANSFER DEVICE), WITH THE RESIDENT, OUT OF THE TUB AND ONTO THE CARRIER (LOWER TRANSFER DEVICE.) AT THIS POINT THE CARETAKER RELEASED THE TRANSFER DEVICE FROM THE TUB. WHEN THE TRANSFER DEVICE WAS PULLED AWAY FROM THE BATHING SYSTEM, THE CHAIR SEPARATED FROM THE CARRIER AND THE RESIDENT AND CHAIR FELL TO THE GROUND. THE RESIDENT WAS NOT SECURED INTO THE CHAIR WITH SAFETY STRAPS, BUT THEY REMAINED IN IT THROUGHOUT THE FALL. THEY WERE TAKEN TO THE ER WHERE THEY WERE TREATED FOR A LACERATION ON THE HEAD THAT DIDN'T REQUIRE STITCHES. THE RESIDENT HAD SOME BRUISING, BUT WAS ABLE TO RETURN TO (B)(6) EXTENDED CARE.

  Patient problems: Bruise/Contusion; Fall; Laceration(s)

  MAUDE report 7026220 ↗