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[Recalled] DOLPHIN INFLATION DEVICE CALIBER INFLATION DEVICE; Catalog Number: CL3030- 018SNA- 018SND 0185NA 0185ND; INTERNAL CODE NUMBER: 0185TR- 0185NA- 018SND 0185NA 0185ND — Complaints regarding broken blister | FDA 2017-04-05
A safety authority has issued a recall or warning for this item. The confirmed facts from the source notice are laid out below.
Recall details
| Product | DOLPHIN INFLATION DEVICE CALIBER INFLATION DEVICE; Catalog Number: CL3030- 018SNA- 018SND 0185NA 0185ND; INTERNAL CODE NUMBER: 0185TR- 0185NA- 018SND 0185NA 0185ND |
|---|---|
| Brand / manufacturer | PEROUSE MEDICAL |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-1891-2017 |
| Country of notice | France |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 05 April 2017 |
| EAN / barcode | 15055430 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Complaints regarding broken blister.
This Class II recall concerns device products distributed in France and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.
What to do if you own this product
Check whether your unit is affected and follow the authority's guidance before further use.
Read the full official notice →
Related recalls from PEROUSE MEDICAL
This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.
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