Anspach Irrigation Clip 40 Recalled Due to Incorrect Assembly
The Anspach Effort, Inc. is recalling 150 Anspach Irrigation Clip 40 units because they were assembled with incorrect, smaller clips.
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 2/5 (Moderate).
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 source text does not report any illnesses or injuries, fitting the criteria for a moderate severity score.
Plain-English summary
The Anspach Effort, Inc. is recalling 150 units of the Anspach Irrigation Clip 40. These medical devices are used to supply controlled, cooling irrigation during the cutting, shaping, and removal of bone, including bones of the skull and spine.
The recall was initiated because the irrigation clips were assembled with incorrect, smaller clips. The affected units are identified by Batch G323082757.
The recall covers distribution in the state of Mississippi. Consumers and healthcare providers should stop using the affected irrigation clips and contact the manufacturer for further instructions.
The recalled product
- Product
- Anspach Irrigation Clip 40 Product Usage: Irrigation clips provide a method of supplying controlled, cooling irrigation during cutting, shaping, and removal of bone, including bones of the skull and spine.
- Manufacturer
- The Anspach Effort, Inc.
- Hazard
- Affected units
- 150
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 (1)
- Batch G323082757.
Distribution
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