International safety notice
Lot recall of acti-fine spine-ject spinal needle pencil point 26 G x 3 1/2 inch / 0,45 x 90 mm with introducer (21 G) 0,8 x 38 mm / sterile, M. Schilling GmbH
Germany / BfArM · DEU · Jul 20, 2016
Key facts
| Title | Lot recall of acti-fine spine-ject spinal needle pencil point 26 G x 3 1/2 inch / 0,45 x 90 mm with introducer (21 G) 0,8 x 38 mm / sterile, M. Schilling GmbH |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Lot recall of acti-fine spine-ject spinal needle pencil point 26 G x 3 1/2 inch / 0,45 x 90 mm with introducer (21 G) 0,8 x 38 mm / sterile, M. Schilling GmbH |
| Manufacturer | Lot recall of acti-fine spine-ject spinal needle pencil point 26 G x 3 1/2 inch / 0,45 x 90 mm with introducer (21 G) 0,8 x 38 mm / sterile, M. Schilling GmbH |
| Models | 6A810, 51-88 |
| Date | Jul 20, 2016 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
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