FDA Device Intelligence
Home › EXMOOR PLASTICS LIMITED › EXMOOR

EXMOOR

EXMOOR PLASTICS LIMITED · Model E402 · UDI-DI 05060180256180

MXP
0
510(k) clearances
5
Adverse events
3
Recalls
18
Facilities

Description

Bone Pate Collector Filters Pack

Recalls

DateFirmReason
2020-12-07Oto Med IncDuring internal Age Testing, holes were found in the sterile Tyvek pouches of the devices.
2020-12-07Oto Med IncDuring internal Age Testing, holes were found in the sterile Tyvek pouches of the devices.
2020-12-07Oto Med IncDuring internal Age Testing, holes were found in the sterile Tyvek pouches of the devices.

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.