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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

recall fda device france

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

ProductDOLPHIN INFLATION DEVICE CALIBER INFLATION DEVICE; Catalog Number: CL3030- 018SNA- 018SND 0185NA 0185ND; INTERNAL CODE NUMBER: 0185TR- 0185NA- 018SND 0185NA 0185ND
Brand / manufacturerPEROUSE MEDICAL
Categorydevice
Issuing authorityFDA_DEVICE
ReferenceZ-1891-2017
Country of noticeFrance
Risk levelClass II
Hazard typerecall
Notice date05 April 2017
EAN / barcode15055430

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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