Anspach Effort Recalls BLACKMAX-NEURO Pneumatic System for Missing Service Interval
The Anspach Effort, Inc. is recalling 25 BLACKMAX-NEURO LOW PRESSURE pneumatic systems because the supplied directions for use did not include 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 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 25 units of the BLACKMAX-NEURO LOW PRESSURE 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 product is identified by Part No. BLACKMAX-N-LP and DFU 18-0040. The recall covers all product shipped prior to 09/27/2016. Distribution was worldwide, including US Nationwide in the states of HI, 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
- BLACKMAX-NEURO LOW PRESSURE Product Usage: Pneumatic system
- Manufacturer
- The Anspach Effort, Inc.
- Hazard
- Affected units
- 25
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 product shipped prior to 09/27/2016
- DFU 18-0040
- Part No. BLACKMAX-N-LP
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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