# FDA recall Z-1896-2021

> **Ossur Americas** · Class II · device recall initiated 2021-06-01.

## Product

OSSUR MIAMI J SELECT COLLAR - Product Usage: is intended to provide gross immobilization to the cervical spine.    REF:  MJS-101;  MJSR-101

## Reason for recall

Due to insufficient column strength of the racks for all load conditions, racks associated with height adjustment functionality have been observed deforming, which may lead to increased range of motion in the cervical spine.

## Distribution

U.S. Nationwide distribution in the states of AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, NE, NJ, NM, NV, NY, OH, OR, PA, Puerto Rico, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, and WV. O.U.S.: Not provided.

## Key facts

- **Recall number:** Z-1896-2021
- **Recalling firm:** Ossur Americas
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2021-06-01
- **Report date:** 2021-06-23
- **Termination date:** 2023-06-22

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Foothill Ranch, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1896-2021

## Citation

> AI Analytics. FDA recall Z-1896-2021. Retrieved 2026-07-16 from https://api.ai-analytics.org/recall/Z-1896-2021. Source: US FDA. Licensed CC0.

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