sertraline hydrochloridedrugHigh PriorityActive

Sertraline Hydrochloride Tablets USP, 100 mg, 90 Tablets bottles, Rx Only, Manufactured by: Lupin Pharmaceuticals, Inc., Naples, FL 34108, NDC 68180-353-09.

sertraline hydrochloride Sertraline Hydrochloride Tablets USP, 100 mg, 90 Tablets bottles, Rx Only, Manufactured by: Lupin Pharmaceuticals, Inc., Naples, FL 34108, NDC 68180-353-09. recalled by FDA. Defective container - seal not adhering to bottles

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: November 5, 2025
Last reviewed by RecallRadar: March 4, 2026

What You Should Do

1## Sertraline Hydrochloride Tablets USP, 100 mg, 90 Tablets bottles, Rx Only, Manufactured by: Lupin Pharmaceuticals, Inc., Naples, FL 34108, NDC 68180-353-
2Agency: FDA | Category: drug Reason: Defective container - seal not adhering to bottles 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 sertraline hydrochloride Devices

What's Being Recalled

Quoted source excerpt from the official notice.

Defective container - seal not adhering to bottles

Who's Affected

Specific models and identifiers listed in the source notice:

Model #1

Lot # QB00865, exp. date Feb 2028

#	Model
1	Lot # QB00865, exp. date Feb 2028

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 sertraline hydrochloride device affected?

Check the affected models section on this page. The official notice currently lists Lot # QB00865, exp. date Feb 2028.

What is the remedy for this recall?

## Sertraline Hydrochloride Tablets USP, 100 mg, 90 Tablets bottles, Rx Only, Manufactured by: Lupin Pharmaceuticals, Inc., Naples, FL 34108, NDC 68180-353-09. Agency: FDA | Category: drug Reason: Defective container - seal not adhering to bottles 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: sertraline hydrochloride recall hub and Food & Drug recall hub.