Medical device recalls Moderate risk

U&I CORP. recalls ANAX 5.5 Poly-Reduction Screw 6.0X50MM, REF: SFNA6050R, part of ANAX 5.5 SPINAL SYSTEM

Recall date
May 26, 2020
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-2672-2020
FDA classification
Class II
Brand / firm
U&I CORP.
Sold / distributed
U.S.: AZ

Why it was recalled

6.0x50mm poly-reduction screws were laser etched 6.0x45

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

ANAX 5.5 Poly-Reduction Screw 6.0X50MM, REF: SFNA6050R, part of ANAX 5.5 SPINAL SYSTEM

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