Total Parental Nutrition - Pediatric PN Patient-Specific TPN Bag, (patient specific), Compound V...

FDA Drug Recall #D-0740-2026 - Class III, July 16, 2026

Recall Summary

Recall Number D-0740-2026
Classification Class III, Low risk
Date Initiated July 16, 2026
Status Ongoing
Voluntary Voluntary: Firm initiated

Recalling Firm

Firm Central Admixture Pharmacy Services Inc
Location Norcross, GA
Product Type Drugs
Quantity (2) patient-specific TPN prescriptions

Product Description

Total Parental Nutrition - Pediatric PN Patient-Specific TPN Bag, (patient specific), Compound Volume 416.8 mL per bag, Rx only, Single Dose Injection, Refrigerated Injection, Central Admixture Pharmacy Services, Inc., Atlanta, 1750 Corp Dr. Ste 725, Norcross, GA 30093 (844) 903-6418

Reason for Recall

Incorrect Product Formulation

Distribution Pattern

GA only

Lot / Code Information

Lot #: 20-1535990-0-1 & 20-1535892-0-1, Exp. Date 16 July 2026

Other Recalls from Central Admixture Pharmacy Services Inc

Recall # Classification Product Date
D-0019-2024 Class II fentaNYL, 100 mcg/2 mL, (50 mcg/mL), 3 mL Syrin... Sep 21, 2023
D-0023-2024 Class II fentaNYL, 5,000 mcg/100 mL, (50 mcg/mL), 100 mL... Sep 21, 2023
D-0027-2024 Class II HYDROmorphone in 0.9% sodium chloride, 6 mg/30 ... Sep 21, 2023
D-0017-2024 Class II fentaNYL 2 mcg/mL and bupivacaine 0.125% PF in ... Sep 21, 2023
D-0030-2024 Class II HYDROmorphone in dextrose 5%, 3 mg/30 mL, (0.1 ... Sep 21, 2023

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.