# FDA recall Z-0508-2021

> **Becton Dickinson & Company** · Class II · device recall initiated 2020-10-23.

## Product

BD Ultra-Fine Pen Needles 32G x 4mm (5/32' )-intended for parenteral administration of a drug from a cartridge contained in a drug pen injector  Catalog Number: 320122

## Reason for recall

Product shelf cartons incorrectly labeled as products intended for the Latin American market. Although the product description on the label  32G x 4mm pen needles  is correct, information pertinent to users in the US regarding compatibility with specific pen needles is missing.

## Distribution

Nationwide

## Key facts

- **Recall number:** Z-0508-2021
- **Recalling firm:** Becton Dickinson & Company
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-10-23
- **Report date:** 2020-12-09
- **Termination date:** 2023-09-08

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Franklin Lakes, NJ, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0508-2021

## Citation

> AI Analytics. FDA recall Z-0508-2021. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/Z-0508-2021. Source: US FDA. Licensed CC0.

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