International safety notice
Recall for SHER-I-SWIV and SHER-I-BRONCH, Teleflex Medical
Germany / BfArM · DEU · Aug 25, 2009
Key facts
| Title | Recall for SHER-I-SWIV and SHER-I-BRONCH, Teleflex Medical |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | SHER-I-SWIV and SHER-I-BRONCH, Teleflex Medical |
| Manufacturer | Recall for SHER-I-SWIV and SHER-I-BRONCH, Teleflex Medical |
| Models | 땅팅6앙은듬, 。읗텅텸輯曁88目8, 5-16041, 06구=MK, 苳털岊昺형호9=-=싶싡능8=월。, V5-16041, V5-16037, 5-16128, 을늘岊岊당음엶苳올일&&필8음§, 蒿8옅춭흔8G8G, 영쿙S유-혛운3춥춍땅흡영~흡운운은윻, 1EFIEX and 25 more |
| Date | Aug 25, 2009 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models in FDA data
- 1–9 Matching catalog numbers in FDA data
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About International device safety notices
Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.
Source: National medical device regulators (as listed), compiled by Orca1