# FDA recall D-0214-2026

> **Safecor Health, LLC** · Class II · drug recall initiated 2025-10-10.

## Product

Haloperidol Lactate Injection, 5 mg/mL, 25 x 1 mL Single-Dose Vials, Sterile, Rx only, For Intramuscular Use Only,  Manufactured for: Mylan Institutional LLC, Morgantown, WV 26605.  NDC: 67457-426-12 with Safecor Health LLC KITCHECK RFID Tag attached with incorrect serial numbers:  KITCHECK 8001-03A3,00000000,003A-2560, and 8001-03A3,00000000,003A-2D3B.

## Reason for recall

Labeling: Not Elsewhere Classified:Incorrect RFID tag labels applied to product by repackaging firm.

## Distribution

Distributed in Massachusetts

## Key facts

- **Recall number:** D-0214-2026
- **Recalling firm:** Safecor Health, LLC
- **Classification:** Class II
- **Product type:** drug
- **Status:** Ongoing
- **Initiation date:** 2025-10-10
- **Report date:** 2025-12-10

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0214-2026

## Citation

> AI Analytics. FDA recall D-0214-2026. Retrieved 2026-09-09 from https://api.ai-analytics.org/recall/D-0214-2026. Source: US FDA. Licensed CC0.

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