Anspach Effort 8.2cm Pneumatic Attachment Recalled for Missing Service Interval
The Anspach Effort, Inc. is recalling 80 units of the 8.2cm Black Max pneumatic attachment because the supplied directions for use did not include a recommended service interval.
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 specific hazard is a documentation error (missing service interval) without reported injuries or illnesses, fitting the criteria for a moderate severity voluntary precautionary recall.
Plain-English summary
The Anspach Effort, Inc. is recalling 80 units of the 8.2cm Attachment, Black Max, which is used in pneumatic systems. The recall was initiated because the supplied Directions for Use (DFU) did not contain a recommended service interval.
The affected units were distributed worldwide, including US nationwide in Hawaii and the District of Columbia, Puerto Rico, Guam, and Japan. The recall covers all serial numbers shipped to customers prior to September 27, 2016, associated with DFU 18-0062 and Part No. B-Violet.
Consumers should stop using the product and contact The Anspach Effort, Inc. for further instructions regarding the missing service interval information.
The recalled product
- Product
- 8.2CM ATTACHMENT, BLACK MAX Product Usage: Pneumatic system
- Manufacturer
- The Anspach Effort, Inc.
- Affected units
- 80
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 (3)
- All serial numbers shipped to customers prior to 09/27/2016
- DFU 18-0062
- Part No. B-Violet.
Distribution
Part of a larger recall action
This product is one of 103 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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