FDA Device recall Z-1939-2016

Maestro Air Motor Pneumatic cranial drill motor

FDA Device
Class II
terminated
Published 2016-06-15

On 2016-06-15 the FDA classified a Class II recall of Maestro Air Motor Pneumatic cranial drill motor by Stryker Instruments Div, citing due to the buildup of grease within the hose and motor, the product may require multiple attempts to start. The grease may also migrate into the attachment end of the motor. There….

Read the official FDA Device notice

Agency	FDA Device
Recall number	Z-1939-2016
Classification	Class II
Status	terminated
Initiated	2016-04-28
Published	2016-06-15
Last updated	2026-09-13 11:54 UTC
Company	Stryker Instruments Div
Distribution	AL, AR, CA, FL, GA, IL, IN, KS, KY, MD, MI, MO, NC, NM, OH, OK, SC, TN, TX, VA, WA, WI

Product

Maestro Air Motor Pneumatic cranial drill motor. The Maestro Air Pneumatic System is a pneumatically operated surgical instrument system. The pneumatic motor provides power to operate removable rotating surgical cutting tools and their accessories.

Reason

Due to the buildup of grease within the hose and motor, the product may require multiple attempts to start. The grease may also migrate into the attachment end of the motor. There is a negligible possibility that the orange grease may leak from the attachment end of the motor and contaminate the surgical wound resulting in soft tissue inflammation.

Identifiers

code_info	Model Number: 5407-200-000 S/N: 1522406703 1522406713 1522406733 1522406743 1522406753 1522406763 1522406773 1522406… Model Number: 5407-200-000 S/N: 1522406703 1522406713 1522406733 1522406743 1522406753 1522406763 1522406773 1522406793 1522406803 1522406813 1522406833 1522406843 1522406853 1522406863 1522406873 1522406883 1522406893 1522406903 1522406923 1523018583 1523018603 1523018623 1523018633 1523018683 1523018713 1523018723 1523018733 1523018743 1523018773 1523018783 1523018813 1523018823 1523018833 1523018843 1523018853 1523018863 1523018873 1523018883 1523018893 1523018903 1523018913 1523601703 1523601723 1523601733 1523601743 1523601763 1523601773 1523601783 1523601793 1523601813 1523601823 1523601833 1523601843 1523601863 1523601873 1523601883 1523601893 1523601903 1523601913 1523601923 1523601933 1523601943 1523904263 1523904273 1523904283 1523904293 1523904303 1523904313 1523904333 1523904343 1523904353 1523904363 1523904373 1523904383 1523904393 1523904403 1523904413 1523904423 1523904433 1523904443 1523904453 1523904463 1523904473 1523904493 1523904503 1523904513 152390452

code_info

Model Number: 5407-200-000 S/N: 1522406703 1522406713 1522406733 1522406743 1522406753 1522406763 1522406773 1522406…

Model Number: 5407-200-000 S/N: 1522406703 1522406713 1522406733 1522406743 1522406753 1522406763 1522406773 1522406793 1522406803 1522406813 1522406833 1522406843 1522406853 1522406863 1522406873 1522406883 1522406893 1522406903 1522406923 1523018583 1523018603 1523018623 1523018633 1523018683 1523018713 1523018723 1523018733 1523018743 1523018773 1523018783 1523018813 1523018823 1523018833 1523018843 1523018853 1523018863 1523018873 1523018883 1523018893 1523018903 1523018913 1523601703 1523601723 1523601733 1523601743 1523601763 1523601773 1523601783 1523601793 1523601813 1523601823 1523601833 1523601843 1523601863 1523601873 1523601883 1523601893 1523601903 1523601913 1523601923 1523601933 1523601943 1523904263 1523904273 1523904283 1523904293 1523904303 1523904313 1523904333 1523904343 1523904353 1523904363 1523904373 1523904383 1523904393 1523904403 1523904413 1523904423 1523904433 1523904443 1523904453 1523904463 1523904473 1523904493 1523904503 1523904513 152390452

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1939-2016%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.