Anspach Effort Recalls IMRI CRANI-A Pneumatic Attachment for Missing Service Interval
The Anspach Effort, Inc. is recalling 10 IMRI CRANI-A pneumatic attachments because the supplied directions for use did not include a recommended service interval.
What this means for you
Cosmetic or documentation issue. No expected health impact, but the manufacturer is correcting the affected products.
Our severity reasoning: The recall is classified as FDA Class II, but the specific defect is a documentation issue (missing service interval) with no reported injuries or illnesses, fitting the 'Low' severity criteria for documentation issues.
Plain-English summary
The Anspach Effort, Inc. is recalling 10 units of the IMRI CRANI-A Attachment, a pneumatic system. The recall is due to a documentation issue where the supplied Directions for Use (DFU) did not contain a recommended service interval.
The affected units are identified by Part No. IMRI-CRANI-A and DFU 18-0093. The recall covers all serial numbers shipped to customers prior to September 27, 2016. Distribution was worldwide, including the United States (specifically HI and DC), Puerto Rico, Guam, and Japan.
Consumers should contact The Anspach Effort, Inc. for further instructions regarding the missing service interval information.
The recalled product
- Product
- IMRI CRANI-A ATTACHMENT Product Usage: Pneumatic system
- 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 prior to 09/27/2016
- DFU 18-0093
- Part No. IMRI-CRANI-A.
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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