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Terminated

Rhinocell Nasal 6.0 x 1.5 x 2.0 w/Airway Catalog #: BMPNP601520A

FDA Recall Z-0486-03 · Posted 2003-01-30

Recalling FirmUltracell Medical Technologies
Recall StatusTerminated
Product CodeEMX
Date Initiated2003-01-08
Date Terminated2012-05-01
Product Quantity100 units

Reason for Recall

Sterility of the device is compromised

Firm Action

Ultracell Medical Technologies initiated the recall by fax or mail on 1/8/03. The firm requested return of product . Distributors were requestd to recall to their accounts.

Root Cause

Other

Distribution Pattern

Nationwide

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

K920358ULTRACELL NASAL PACKINGUltracell Medical Technologies, Inc. · 1992-11-30

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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