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Aspiration Tubing

ARMM INC. · Model 51412 · UDI-DI 10850082007124

KDH Prescription
1
510(k) clearances
66
Adverse events (6 deaths)
2
Recalls
11
Facilities

Description

Aspiration Tubing - 12'

Recalls

DateFirmReason
2024-02-23MEDLINE INDUSTRIES, LP - NorthfieldProduct may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users.
2012-05-10MEDDEV USA, INC.The device was marketed without a 510(k) and is not sterile.

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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.