PEROUSE MEDICAL: Medical Device Recall in 2017 - (Recall #: Z-1891-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

DOLPHIN INFLATION DEVICE CALIBER INFLATION DEVICE; Catalog Number: CL3030- 018SNA- 018SND 0185NA 0185ND; INTERNAL CODE NUMBER: 0185TR- 0185NA- 018SND 0185NA 0185ND

Product Classification:

Class II

Date Initiated: April 5, 2017

Date Posted: May 10, 2017

Recall Number: Z-1891-2017

Event ID: 77100

Reason for Recall:

Complaints regarding broken blister.

Status: Terminated

Product Quantity: 18,431

Code Information:

1 5045606 - 15055430 - 15065340 - 15065685 -15065744- 15065858- 15065970- 15075121 - 15075265 - 15075411- 15075821 - 1 5075851 - 15075942 - 15085001 - 15085075 -15085378- 15085435 -15085515- 15085555 -15105052- 15125214- 16015267- 16025034- 16025640

Distribution Pattern:

US: AZ (shipped through Belgium to USA), MN, TN

Voluntary or Mandated:

Voluntary: Firm initiated