oxycodone hydrochloridedrugHigh PriorityActive

Oxycodone Hydrochloride Tablets, USP (CII), 5 mg, 100-Count (10 x 10) blister cards per carton, Rx Only, The drug product contained in this package is from NDC # 10702-018, KVK-Tech Inc. Distributed by: American Health Packaging, Columbus, Ohio 43217, Carton NDC 68084-354-01; Blister NDC 68084-354-11

Oxycodone Hydrochloride Tablets, USP (CII), 5 mg, 100-Count (10 x 10) blister cards per carton, Rx Only, The drug product contained in this package is from NDC # 10702-018, KVK-Tech Inc. Distributed by: American Health Packaging, Columbus, Ohio 43217, Carton NDC 68084-354-01; Blister NDC 68084-354-11 was recalled because defective container: multiple customer complaints received for card seal defects observed on the subject lots. customers reported card seal defects (weak/non-existent seals), leading to the tablets falling out of their cavities.. If you have this product, stop using it until you verify your lot or model details.

By RecallRadar Editorial Team

Sourced from FDA. Last verified March 15, 2026.

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Key facts

Date announced: February 18, 2026
Source agency: FDA

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.

What's Being Recalled

Quoted source excerpt from the official notice.

Defective container: Multiple customer complaints received for card seal defects observed on the subject lots. Customers reported card seal defects (weak/non-existent seals), leading to the tablets falling out of their cavities.

Quick Info

Key facts from the official notice, kept in the article flow for easy cross-checking.

Brand: Oxycodone hydrochloride
Category: drug
Source agency: FDA
Announced: February 18, 2026
Country: US
Status: Active

Who's Affected

Specific models and identifiers listed in the source notice:

Model #1

Lots #: 1027932, Exp Date 06/30/2027, 1028360, Exp Date 08/31/2027

#	Model
1	Lots #: 1027932, Exp Date 06/30/2027, 1028360, Exp Date 08/31/2027

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

What You Should Do

Follow the remedy path from the official notice using the exact model and serial details above.

1Stop using the affected product until you verify whether your item is impacted.
2Check the official recall notice and match your model, lot, or serial details.
3Follow the official instructions for repair, replacement, refund, or disposal.

Open Official Recall Notice Get Alerts for oxycodone hydrochloride Devices

Source & Verification

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

Official source: FDA
Announced by source: February 18, 2026
Last reviewed by RecallRadar: March 15, 2026

Frequently Asked Questions

Am I affected by this recall?

Check the affected models section on this page. The official notice currently lists Lots #: 1027932, Exp Date 06/30/2027, 1028360, Exp Date 08/31/2027.

What is the remedy for this recall?

Follow the official instructions for repair, replacement, refund, or disposal on the oxycodone hydrochloride recall page.

Where can I verify recall details?

Use the official source link in this page to confirm dates, eligibility, and next steps: https://api.fda.gov/drug/enforcement.json?search=recall_number:D-0338-2026&limit=1

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