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InHealth Technologies; Blom-Singer; Classic

Freudenberg Medical, LLC · Model IN 2008-LF · UDI-DI 00813307014201

EPEEWL Prescription
2
510(k) clearances
6
Adverse events
1
Recalls
67
Facilities

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.

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

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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.