# FDA recall D-1062-2016

> **Lyne Laboratories, Inc.** · Class III · drug recall initiated 2016-06-07.

## Product

Cyproheptadine Hydrochloride Syrup, Oral Solution USP, 2 mg/5 mL, packaged in an amber glass 473 mL (one pint) bottle with child-resistant screw closure, Rx only, Distributed by: Rising Pharmaceuticals, Inc., Allendale, NJ 07401, Manufactured by: Lyne Laboratories, Inc., Brockton, MA 02301, NDC 64980-0504-48

## Reason for recall

Subpotency: product assayed and found OOS for cyproheptadine

## Distribution

NJ

## Key facts

- **Recall number:** D-1062-2016
- **Recalling firm:** Lyne Laboratories, Inc.
- **Classification:** Class III
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2016-06-07
- **Report date:** 2016-07-13
- **Termination date:** 2017-02-03

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1062-2016

## Citation

> AI Analytics. FDA recall D-1062-2016. Retrieved 2026-05-27 from https://api.ai-analytics.org/recall/D-1062-2016. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*
