# FDA recall Z-1123-2019

> **Encore Medical, Lp** · Class II · device recall initiated 2018-09-21.

## Product

Exprt Precision System: Revision Hip, Proximal Body with Bolt, Lateral Offset, Sterile R, djo surgical,    REF: 495-00-065,  495-00-075,  495-00-085,   495-01-065, 495-01-075, 495-01-085

## Reason for recall

Complaints regarding loose proximal body bolts or bolts that were found through x-ray as sitting above the proximal body and not properly seated. Patient risks may include: pain, dissociation, and possible revision surgery

## Distribution

US: TN, MN, TX, CO, IL, IN, OH, SC, MS, MI, RI, PA, ME, NY, WA, MO, AR, OK, LA, AL, FL, GA, UT, AZ, CA, NV,.

## Key facts

- **Recall number:** Z-1123-2019
- **Recalling firm:** Encore Medical, Lp
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2018-09-21
- **Report date:** 2019-04-17
- **Termination date:** 2020-09-16

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Austin, TX, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1123-2019

## Citation

> AI Analytics. FDA recall Z-1123-2019. Retrieved 2026-07-26 from https://api.ai-analytics.org/recall/Z-1123-2019. Source: US FDA. Licensed CC0.

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