Anspach Effort Pneumatic System Attachment Recalled for Missing Service Interval
The Anspach Effort, Inc. is recalling 10.5cm Long Attachments for pneumatic systems because the supplied directions for use did not contain 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. The hazard is a documentation issue (missing service interval) rather than a direct physical defect or reported injury, fitting the criteria for a moderate severity voluntary precautionary recall.
Plain-English summary
The Anspach Effort, Inc. is recalling 10.5cm Long Attachments, Non-Tapered End, used in pneumatic systems. The recall involves 4 units. The product was distributed worldwide, including in the United States (specifically HI and DC), Puerto Rico, Guam, and Japan.
The recall was initiated because the supplied Directions for Use (DFU) did not contain a recommended service interval. The affected units are identified by Part No. LONG-01 and DFU 18-0048. The recall includes all serial numbers shipped to customers prior to 09/27/2016.
Consumers who have this product should contact The Anspach Effort, Inc. for instructions on how to proceed.
The recalled product
- Product
- 10.5cm Long Attachment, Non-Tapered End Product Usage: Pneumatic system
- Manufacturer
- The Anspach Effort, Inc.
- Hazard
- Affected units
- 4
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 18-0048
- Part No. LONG-01.
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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