The Anspach Effort, Inc.: Medical Device Recall in 2016 - (Recall #: Z-2783-2016)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

Light Adaptor for Small Battery Drive and Small Battery Drive II.

Product Classification:

Class I

Date Initiated: June 24, 2016

Date Posted: October 5, 2016

Recall Number: Z-2783-2016

Event ID: 74835

Reason for Recall:

There was a potential for the Adaptor and Light Adaptor for Small Battery Drive and Small Battery Drive II to generate excessive internal pressure that may cause the products to burst.

Status: Terminated

Product Quantity: 1,833 devices (05.001.024 and 05.001.108)

Code Information:

Model/Catalog: Part # (05.001.108 and 05.001.024) Serial: All Serial Numbers.

Distribution Pattern:

Worldwide Distribution - US Nationwide and including the countries of Canada, Austria, Australia, Belgium, Brazil, Chile, China, Colombia, Costa Rica, Czech Republic, Denmark, Finland, France, Germany, Hong Kong, Hungary, India, Indonesia, Ireland, Israel, Italy, Japan, Jordan, Kuwait, Libya, Malaysia, Mexico, Nepal, Netherlands, New Zealand, Norway, Poland, Portugal, Romania, Russia, Saudi Arabia, Singapore, Slovenia, Slovakia, Spain, South Africa, South Korea, Sri Lanka, Sweden, Switzerland, Taiwan, Thailand, Turkey, United Arab Emirates, United Kingdom, and Vietnam, and areas of Middle East, Africa, Asia & Pacific.

Voluntary or Mandated:

Voluntary: Firm initiated