International safety notice
Recall of various sterile gauze products, Paul Hartmann AG
Germany / BfArM · DEU · May 16, 2012
Key facts
| Title | Recall of various sterile gauze products, Paul Hartmann AG |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recall of various sterile gauze products, Paul Hartmann AG |
| Manufacturer | Recall of various sterile gauze products, Paul Hartmann AG |
| Models | 4701149, 2950111, 4750672, P30X20, 4512098, 4701899, 4501034, 4522337, 1XXX53XXX, P15X30, 89522, 4511039 and 157 more |
| Date | May 16, 2012 |
| 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