Anspach Effort 90 Degree Contra Angle Attachment Recalled for Missing Service Interval
The Anspach Effort, Inc. is recalling 90 degree Contra Angle Attachments 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, and the hazard is a documentation issue (missing service interval) rather than a direct physical defect or reported injury, fitting the criteria for moderate severity.
Plain-English summary
The Anspach Effort, Inc. is recalling 90 degree Contra Angle Attachments used in pneumatic systems. The recall was initiated because the supplied directions for use (DFU) did not contain a recommended service interval.
The affected products are identified by Part No. ORANGE-90 and DFU 18-0030. The recall includes all serial numbers shipped to customers prior to 09/27/2016. These products were distributed worldwide, including US Nationwide in the states of HI, DC, Puerto Rico, Guam, and Japan.
Consumers should stop using the affected attachments and contact The Anspach Effort, Inc. for further instructions regarding the missing service interval information.
The recalled product
- Product
- 90 degree Contra Angle Attachment Product Usage: Pneumatic system
- Manufacturer
- The Anspach Effort, Inc.
- Hazard
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 18-0030
- Part No. ORANGE-90.
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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