Crossroads Extremity Systems Llc recalls MotoCLIP(TM) Super Elastic Fusion System, Size 18mm x 14mm x 14mm, REF 1442-1814, Rx Only, STERILE R.
- Recall date
- February 16, 2017
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-1487-2017
- FDA classification
- Class II
- Brand / firm
- Crossroads Extremity Systems Llc
- Sold / distributed
- Al, FL, IN, Il, NE, TX, NM, CO, AZ
Why it was recalled
Seven 18mm x 18mm x 18 mm implants had been placed in kits, packed and labeled as 18mm x 14mm x 14mm.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
MotoCLIP(TM) Super Elastic Fusion System, Size 18mm x 14mm x 14mm, REF 1442-1814, Rx Only, STERILE R.
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