Z-2783-2016 Class I Terminated
FDA device recall Z-2783-2016 was initiated by The Anspach Effort, Inc. on Jun 24, 2016 and is designated Class I. 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. The recall status is terminated (terminated Jun 9, 2018). Affected quantity: 1,833 devices (05.001.024 and 05.001.108).
Recall Details
- Product Type
- Devices
- Report Date
- Oct 5, 2016
- Initiation Date
- Jun 24, 2016
- Termination Date
- Jun 9, 2018
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 1,833 devices (05.001.024 and 05.001.108)
Product Description
Reason for Recall
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.
Code Information
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-2783-2016
- openFDA file date
- Oct 23, 2026
- Loaded by RegDataLab
- Oct 26, 2026