Limacorporate SMR Allen Wrench Recalled for Dimensional Non-Conformance
Limacorporate S.p.A is recalling 76 SMR allen wrenches (5 mm) because they are dimensionally non-conforming and may not function with some T-handles.
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 for a dimensional non-conformance that affects functionality but does not present a risk of serious injury or death, fitting the criteria for a low-severity issue.
Plain-English summary
Limacorporate S.p.A is recalling 76 units of the SMR allen wrench 5 mm (product code 9013.50.210). The recall was initiated because the product was found to be dimensionally non-conforming, specifically being slightly over dimensioned on the diameter of the Zimmer connection.
This dimensional issue renders the wrench non-functional for connecting with some T-handles. The affected units were distributed in the US, Italy, and Australia. The specific code for the recalled units is 14AA311.
Consumers who possess this product should stop using it and contact the recalling firm for further instructions.
The recalled product
- Product
- SMR allen wrench 5 mm, product code 9013.50.210
- Manufacturer
- Limacorporate S.p.A
- Affected units
- 76
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)
- 14AA311
Distribution
Distribution scope not specified by the agency.
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