The Anspach Effort, Inc.: Medical Device Recall in 2015 - (Recall #: Z-2345-2015)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2015.

Data Source: FDA.

Product Description:

Synthes Battery Power Line II Oscillator Model 530.710, orthopedic surgical power tool.

Product Classification:

Class II

Date Initiated: July 1, 2015

Date Posted: August 12, 2015

Recall Number: Z-2345-2015

Event ID: 71659

Reason for Recall:

Saw head separated from the drive unit or began to come loose.

Status: Terminated

Product Quantity: 360 handpieces (Currently there are 9 affected units remaining in the US and 17 units OUS all others were reworked)

Code Information:

Serial numbers: 100067, 100076, 100371, 100372, 100063, 100065, 100069, 100076, and 100055; Foreign: Item number 530.710 Serial numbers: 100020, 100026, 100039, 100248, 100254, 100257, 100263, 100265, 100269, 100270, 100293, 100296, 100307, 100313, 100315, 100339, and 100340.

Distribution Pattern:

Worldwide Distribution - US Distribution to the states of : AR, LA, OH, and WA., and the countries of : China, France, Italy, Russia, South Africa, Switzerland, and United Kingdom.

Voluntary or Mandated:

Voluntary: Firm initiated