trazodone hydrochloridedrugHigh PriorityActive

Trazodone Hydrochloride, USP, 50 mg, 100-Count Bottle, Rx only, Manufactured by: Granules India Limited, Hyderabad, 500 081, India, Manufactured for: Granules Pharmaceuticals Inc., Chantilly, VA 20151, NDC 70010-231-01.

trazodone hydrochloride Trazodone Hydrochloride, USP, 50 mg, 100-Count Bottle, Rx only, Manufactured by: Granules India Limited, Hyderabad, 500 081, India, Manufactured for: Granules Pharmaceuticals Inc., Chantilly, VA 20151, NDC 70010-231-01. recalled by FDA. Presence of Foreign Tablets/Capsules

By RecallRadar Editorial Team

Sourced from FDA. Last reviewed March 4, 2026.

This recall involves safety concerns. Take action promptly.

✨ Plain-English Summary

Is This Recall Still Active?

Status: Yes - Active

This recall is currently active. If your device matches the affected models, follow the official instructions as soon as possible.

Source & Verification

This page summarizes the official notice and keeps key facts easy to verify.

Official source: FDA
Announced by source: January 26, 2026
Last reviewed by RecallRadar: March 4, 2026

What You Should Do

1## Trazodone Hydrochloride, USP, 50 mg, 100-Count Bottle, Rx only, Manufactured by: Granules India Limited, Hyderabad, 500 081, India, Manufactured for: Granules Pharmaceuticals Inc., Chantilly, VA 20151, NDC 70010-231-
2Agency: FDA | Category: drug Reason: Presence of Foreign Tablets/Capsules What to do:
3Stop using the product if your lot/model matches.
4Check the FDA notice for specifics.

Open Official Recall Notice Get Alerts for trazodone hydrochloride Devices

What's Being Recalled

Quoted source excerpt from the official notice.

Presence of Foreign Tablets/Capsules

Who's Affected

Specific models and identifiers listed in the source notice:

Model #1

Batch # 6160008A, Exp Date: 12/31/2026

#	Model
1	Batch # 6160008A, Exp Date: 12/31/2026

Technical model codes are manufacturer identifiers. Match both the product name and model code from your device settings, label, or packaging.

Frequently Asked Questions

Is my trazodone hydrochloride device affected?

Check the affected models section on this page. The official notice currently lists Batch # 6160008A, Exp Date: 12/31/2026.

What is the remedy for this recall?

## Trazodone Hydrochloride, USP, 50 mg, 100-Count Bottle, Rx only, Manufactured by: Granules India Limited, Hyderabad, 500 081, India, Manufactured for: Granules Pharmaceuticals Inc., Chantilly, VA 20151, NDC 70010-231-01. Agency: FDA | Category: drug Reason: Presence of Foreign Tablets/Capsules What to do: 1. Stop using the product if your lot/model matches. 2. Check the FDA notice for specifics. 3. Follow remedy instructions.

Where can I verify recall details?

Use the official source link in this page to confirm dates, eligibility, and next steps: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Keep browsing with these internal hubs: trazodone hydrochloride recall hub and Food & Drug recall hub.