Hydrocortisone and Acetic Acid Otic Solution, USP, 10 mL per dropper bottle, Rx only, Hi-Tech Pha...

FDA Drug Recall #D-1011-2019 — Class II — March 12, 2019

Recall Summary

Recall Number D-1011-2019
Classification Class II — Moderate risk
Date Initiated March 12, 2019
Status Terminated
Voluntary Voluntary: Firm initiated

Recalling Firm

Firm Akorn Inc
Location Lake Forest, IL
Product Type Drugs
Quantity 15,322 10 ml bottles

Product Description

Hydrocortisone and Acetic Acid Otic Solution, USP, 10 mL per dropper bottle, Rx only, Hi-Tech Pharmacal Co, Inc., Amityville, NY 11701. NDC: 50383-901-10

Reason for Recall

Sub Potent Drug: OOS results observed for the Hydrocortisone assay during routine stability testing at 12 month controlled room temperature.

Distribution Pattern

Nationwide USA and Puerto Rico

Lot / Code Information

Lot: 357647, EXP 04/2019

Other Recalls from Akorn Inc

Recall # Classification Product Date
D-1258-2020 Class III Fentanyl Citrate Injection, USP, 100 mcg/2 mL (... Mar 25, 2020
D-0839-2020 Class II Hydrocortisone and Acetic Acid Otic Solution, U... Dec 16, 2019
D-1392-2019 Class III Myorisan (isotretinoin capsules, USP), 40 mg, p... Jun 7, 2019
D-1241-2019 Class III Fentanyl Citrate Injection, USP, 100 mcg/2 mL (... Apr 23, 2019
D-0511-2019 Class II Moisturizing Lubricant Eye Drops, 0.25% Sodium ... Feb 4, 2019

Frequently Asked Questions

Stop taking the medication and contact your pharmacist or doctor immediately. For Class I recalls, this is urgent. For Class II or III recalls, consult your doctor before stopping — abruptly discontinuing certain medications (blood pressure drugs, antidepressants, diabetes medications) can be more harmful than continuing while arranging a replacement. Check whether the recall applies to your specific lot number and expiration date. Return the product to your pharmacy and report any adverse effects to FDA MedWatch at 1-800-FDA-1088.

Not necessarily. Many drug recalls are initiated because of quality system failures or test results that suggest a product might not meet specifications — even if no patients have reported harm. The FDA uses a precautionary approach: if there is reason to believe quality standards were not met, a recall is required regardless of whether adverse effects have been reported. Class I recalls typically involve a reasonable probability of harm; Class II recalls may cause temporary health issues; Class III recalls are for products unlikely to cause adverse health consequences but that still violate regulations.

Pharmacies typically receive recall notices directly from drug wholesalers and manufacturers within days of the recall being announced. Your pharmacist can look up whether any product in your prescription history matches a recalled lot number. For current recalls, the FDA publishes updates at FDA.gov/safety/recalls-market-withdrawals-safety-alerts and sends MedWatch email alerts for significant drug safety issues. You can sign up for MedWatch alerts at FDA.gov. Most major pharmacy chains also have their own recall notification systems that automatically alert pharmacists when a recalled product is in their inventory.

What Should You Do?

Stop using this medication if affected by this recall. Contact your pharmacist or prescribing doctor immediately for guidance. Do not flush medications — use a drug take-back program.