Anspach Effort Recalls 90 Degree Right Angle Attachments for Missing Service Interval
The Anspach Effort, Inc. is recalling 10 units of the 90 Degree Right Angle Attach, Black Max, because the supplied directions for use did not contain a recommended service interval.
The agency’s classification
FDA (Devices): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 1/5 (Low).
Cosmetic or documentation issue. No expected health impact, but the manufacturer is correcting the affected products.
Our severity reasoning: The recall is classified as Low severity because the issue is a documentation error (missing service interval) with no reported injuries or illnesses, fitting the rubric criteria for documentation issues.
Plain-English summary
The Anspach Effort, Inc. is recalling 10 units of the 90 Degree Right Angle Attach, Black Max. The recall is due to a documentation issue where the supplied directions for use (DFU) did not contain a recommended service interval.
The affected product is identified by Part No. B-ORANGE-90 and DFU 18-0062. The units were distributed worldwide, including the US nationwide in the states of HI and DC, Puerto Rico, Guam, and Japan. All serial numbers were shipped to customers.
Consumers should stop using the product and contact The Anspach Effort, Inc. for further instructions.
The recalled product
- Product
- 90 DEG RIGHT ANGLE ATTACH, BLACK MAX
- Manufacturer
- The Anspach Effort, Inc.
- Hazard
- Affected units
- 10
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
- DFU 18-0062
- Part No. B-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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