# FDA recall Z-2948-2020

> **MicroPort Orthopedics Inc.** · Class II · device recall initiated 2020-07-31.

## Product

PROFEMUR Titanium and Cobalt Chrome modular necks, Item Numbers and descriptions:  Item Number	Description	Description 2  PHAC1202	PROFEMUR NECK NEUTRAL	SHORT COBALT CHROME  PHAC1204	PROFEMUR NECK NEUTRAL	LONG COBALT CHROME  PHAC1212	PROFEMUR NECK A/R VAR/VAL 2	SHORT COBALT CHROME  PHAC1214	PROFEMUR NECK A/R VAR/VAL 2	LONG COBALT CHROME  PHAC1222	PROFEMUR NECK A/R VAR/VAL 1	SHORT COBALT CHROME  PHAC1224	PROFEMUR NECK A/R VAR/VAL 1	LONG COBALT CHROME  PHAC1232	PROFEMUR NECK A/R 8DG	SHORT COBALT CHROME  PHAC1234	PROFEMUR NECK A/R 8DG	LONG COBALT CHROME  PHAC1242	PROFEMUR NECK A/R 15DG	SHORT COBALT CHROME  PHAC1244	PROFEMUR NECK A/R 15DG	LONG COBALT CHROME  PHAC1252	PROFEMUR NECK VAR/VAL 8DG	SHORT COBALT CHROME  PHA01202	PROFEMUR NECK NEUTRALSHORT	SHORT  PHA01204	PROFEMUR NECK NEUTRAL	LONG  PHA01206	PROFEMUR NECK NEUTRAL	X LONG  PHA01212	PROFEMUR NECK A/R VAR/VAL 2	SHORT  PHA01214	PROFEMUR NECK A/R VAR/VAL 2	LONG  PHA01222	PROFEMUR NECK A/R VAR/VAL 1	SHORT  PHA01224	PROFEMUR NECK A/R VAR/

## Reason for recall

MicroPort Orthopedics Inc. is voluntarily recalling any existing inventory of PROFEMUR¿ Titanium and Cobalt Chrome modular necks with previous package insert versions to replace the PROFEMUR¿ Hip System Package Insert with the most recent revision (150803-8).

## Distribution

Worldwide Distribution: US (nationwide) to states of: AL, AZ, CA, CO, FL, GA,  IA, ID, IL, IN, KS, MA, MD, MI, MO, MT, NC, NH, NJ, NV, OH, PA, TN, TX, UT, VA,  WA, WI including PR; and countries of: Brazil, Canada, China, Costa Rica, France, Germany, Japan, The Netherlands and United Kingdom.

## Key facts

- **Recall number:** Z-2948-2020
- **Recalling firm:** MicroPort Orthopedics Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2020-07-31
- **Report date:** 2020-09-16

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Arlington, TN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2948-2020

## Citation

> AI Analytics. FDA recall Z-2948-2020. Retrieved 2026-07-02 from https://api.ai-analytics.org/recall/Z-2948-2020. Source: US FDA. Licensed CC0.

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