FDA recall record

Integra LifeSciences The humeral stems trials are packaged in a kit for Titan Modular recall — FDA Z-1463-2018

Incidents of stem trial breakage were reported to the firm suggesting that these fractures all occurred during insertion/impaction or extraction of the…

Class IIclassification
Z-1463-2018official record ID
May 2, 2018report date

Recall record at a glance

Official recordZ-1463-2018
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmIntegra LifeSciences Corp.
Report dateMay 2, 2018
Recall initiation dateDec 20, 2017
Quantity1619 units
LocationPlainsboro, NJ, United States

Official product description

The humeral stems trials are packaged in a kit for Titan Modular Shoulder System under the following labeling: Catalog Number Product Description TRL092002506 Humeral Stem Trial, 6mm TRL092002507 Humeral Stem Trial, 7mm TRL092002508 Humeral Stem Trial, 8mm TRL092002509 Humeral Stem Trial, 9mm TRL092002510 Humeral Stem Trial, 10mm TRL092002511 Humeral Stem Trial, 11mm TRL092002512 Humeral Stem Trial, 12mm TRL092002513 Humeral Stem Trial, 13mm TRL092002514 Humeral Stem Trial, 14mm TRL092002515 Humeral Stem Trial, 15mm TRL092002516 Humeral Stem Trial, 16mm

Why the product was recalled

Incidents of stem trial breakage were reported to the firm suggesting that these fractures all occurred during insertion/impaction or extraction of the humeral stem trial whiling preparing the humeral canal and/or trialing. All cases resulted in a delay in surgery, with a variance of medical intervention required.

Distribution information

Worldwide Distribution - USA (nationwide) Distribution.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

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