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Z-2619-2023 Class II Ongoing

Recalled by R A Medical Services — Keighley

FDA device recall Z-2619-2023 was initiated by R A Medical Services on August 23, 2023 and is designated Class II. Reason for recall: Inadequate documentation of acceptance activity The recall status is ongoing. Affected quantity: 10 units.

Recall Details

Product Type: Devices
Report Date: September 27, 2023
Initiation Date: August 23, 2023
Termination Date: N/A
Voluntary/Mandated: Voluntary: Firm initiated
Product Quantity: 10 units

Product Description

MINISCAV (tm) Vacuum Pump

Reason for Recall

Inadequate documentation of acceptance activity

Distribution Pattern

Distribution to Ohio

Code Information

UDI/DI: (01) 10862552000405. Serial numbers: N/AB/10514 through N/AB/10523