Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
19cm Attachment Recalled by The Anspach Effort, Inc. Due to Supplied Directions for Use (DFU) did not contain...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact The Anspach Effort, Inc. directly.
Affected Products
19cm Attachment, Black Max Product Usage: Pneumatic system
Quantity: 41
Why Was This Recalled?
Supplied Directions for Use (DFU) did not contain a recommended service interval.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About The Anspach Effort, Inc.
The Anspach Effort, Inc. has 261 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report