FDA Device Intelligence
HomeHausmann Enterprises, LLC › PT,SINGLE TAPING MODULE,42hx28wx42d

PT,SINGLE TAPING MODULE,42hx28wx42d

Hausmann Enterprises, LLC · Model A9401 · UDI-DI 00840314810076

KMN
3
510(k) clearances
128
Adverse events (3 deaths)
3
Recalls
188
Facilities

Recalls

DateFirmReason
2021-05-12Stryker Medical Division of Stryker CorporationMedical devices intended for use in a healthcare facility were distributed to residential customers and may be in use in a home environment. The product s labeling accurately iden
2021-05-12Stryker Medical Division of Stryker CorporationMedical devices intended for use in a healthcare facility were distributed to residential customers and may be in use in a home environment. The product s labeling accurately iden
2012-08-06Invacare CorporationOn August 6, 2012, Invacare voluntarily recalled the Invacare I-Fit" Shower Chair (Models 9780, 9781, 9781-1) based on the return, quality and adverse event data received.

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.