# FDA recall Z-1756-2020

> **Smith & Nephew, Inc.** · Class II · device recall initiated 2020-03-17.

## Product

Smith & Nephew FOOTPRINT ULTRA PK SUTURE ANCHOR 4.5  Part Number: 72202901

## Reason for recall

Space between the device and the packaging permits excessive movement which could potentially lead to the displacement of the anchors tip protector allowing the tip of the anchor to create a sterile breach.

## Distribution

Nationwide  Foreign:  AE  AL  AR  AT  AU  BE  BM  BR  CA  CH  CL  CN  CO  CR  CZ  DE  DK  EC  EE  ES  FI  FR  GB  IE  IL  IN  IT  KR  LT  LV  MT  MX  NO  PA  PE  PL  PR  PT  QA  RU  SE  SG  TH  TR  XK  ZA

## Key facts

- **Recall number:** Z-1756-2020
- **Recalling firm:** Smith & Nephew, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2020-03-17
- **Report date:** 2020-04-29

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Mansfield, MA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1756-2020

## Citation

> AI Analytics. FDA recall Z-1756-2020. Retrieved 2026-06-30 from https://api.ai-analytics.org/recall/Z-1756-2020. Source: US FDA. Licensed CC0.

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