Anspach G1 Dissection Tools Recalled for Inconsistent Shaft Exposure Labeling
The Anspach Effort, Inc. is recalling 686 G1 dissection tools because the specified shaft exposure may be greater than labeled when used with certain attachments.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II, but the source text describes a labeling inconsistency regarding shaft exposure without reporting any injuries, illnesses, or deaths. This aligns with the rubric for moderate severity involving labeling errors or theoretical risks without reported harm.
Plain-English summary
The Anspach Effort, Inc. is recalling 686 units of the ANSPACH 3MM Fluted Matchstick (REF S-8NS-M-G1) dissection tools. These tools are used for cutting and shaping bone, including the spine and cranium.
The recall is due to a labeling inconsistency. The G1 dissection tools are not compatible with all attachments listed on the labeling. Additionally, the tools are labeled with a Specified Shaft Exposure that may not be consistent when used with each attachment on the product label, meaning the actual shaft exposure may be greater than indicated.
The affected tools were distributed worldwide, including in the United States (AZ, CA, CO, FL, GA, IL, KY, LA, MN, MO, NC, NJ, NY, OH, OR, PA, TX) and internationally to Canada and China. All lot numbers are affected. Users should stop using these tools and contact the recalling firm for instructions.
The recalled product
- Product
- ANSPACH - 3MM Fluted Matchstick, Extends 8.9MM, Less Aggressive; REF S-8NS-M-G1 Cutting shaping bone including spine and cranium.
- Manufacturer
- The Anspach Effort, Inc.
- Affected units
- 686
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (2)
- REF S-8NS-M-G1
- ALL lot numbers.
Distribution
Part of a larger recall action
This product is one of 34 recalled by The Anspach Effort, Inc. under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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