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Home3M Deutschland GmbH › 3M™ Tegaderm™

3M™ Tegaderm™

3M Deutschland GmbH · Model 1655 · UDI-DI 00707387807771

KMK
10
510(k) clearances
767
Adverse events (5 deaths)
7
Recalls
201
Facilities

Description

3M™ Tegaderm™ Transparent Film Dressing with Border, 1655, 3-1/2 in x 4-1/2 in (6.9 cm x 11.5 cm), 50/ct 4ct/Case

Recalls

DateFirmReason
2017-04-25Bard Access Systems Inc.StatLockTM IV Premium Catheter Stabilization Device may contain an incorrectly sized retainer clip.
2016-12-09Bard Access SystemsBard Access Systems announces a voluntary field action for the StatLock Catheter Stabilization Devices because some single unit pouches have been released without unique product id
2016-12-09Bard Access SystemsBard Access Systems announces a voluntary field action for the StatLock Catheter Stabilization Devices because some single unit pouches have been released without unique product id
2013-06-10Bard Access SystemsBARD Access Systems is recalling lot JUWJF283 of StatLock CV Plus Stabilization Butterfly Devices due to incorrect pad assembly used during manufacture. The absence of the hydrocol
2007-02-15Merit Medical Systems, IncSterility of some units may be compromised due to damaged packaging.
2007-02-15Merit Medical Systems, IncSterility of some units may be compromised due to damaged packaging.
2007-02-15Merit Medical Systems, IncSterility of some units may be compromised due to damaged packaging.

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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.