PlainRecalls
ModerateClass IIOngoing

FDA Drug recall · Reported May 13, 2026

TPN bag (patient specific), Rx# 11-4909703-0-1, Compound Volume 1660 mL per bag, Rx only, Single Dose Injection, Refrigerated Injection, Central Admixture Pharmacy Services, Los Angeles, 13128 Imperial Hwy, Santa Fe Spr., CA 90670

Incorrect Product Formulation: product did not contain insulin as listed in the label.

Recall #
D-0524-2026
Affected scope
1 bag
Initiated
December 27, 2025
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The recall

Central Admixture Pharmacy Services, Inc (Caps) Los Angeles issued this moderate-severity FDA Drug recall — Incorrect Product Formulation: product did not contain insulin as listed in the label..

Moderate
severity level
Class II
classification
May 13, 2026
reported

Sourced from official FDA Drug enforcement records. Verify recall #D-0524-2026 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.

Recall Insight

This FDA Drug action (record #D-0524-2026) was formally reported on May 13, 2026, with the manufacturer initiating the action on December 27, 2025. It is classified under Moderate severity (Class II), with a current status of Ongoing. Central Admixture Pharmacy Services, Inc (Caps) Los Angeles is listed as the recalling firm, operating out of Santa Fe Springs, CA. Federal records list the affected scope as 1 bag.

The documented reason for this recall is: Incorrect Product Formulation: product did not contain insulin as listed in the label. Distribution data in the federal record shows the product reached: CA. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.

Within the same product category the archive holds 6 closely related recalls, 5 from FDA Drug — clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.

Drugs & Medications recalls over time

Where this recall sits in its category — 14,048 drugs & medications recalls on record

-50005001,0001,5002,000 20052009201220152018202120242026 216

Where this recall sits in the database

Severity2366872097High severity (most serious)Moderate severityLow severity
Where this recall sits in the database

Of 100,165 recalls in the database, 23,668 are high severity, 72,097 moderate, and 4,400 low. This recall is classified moderate severity.

Severity

Moderate

Affected scope

1 bag

Related Recalls

6

5 from same agency

Product description

TPN bag (patient specific), Rx# 11-4909703-0-1, Compound Volume 1660 mL per bag, Rx only, Single Dose Injection, Refrigerated Injection, Central Admixture Pharmacy Services, Los Angeles, 13128 Imperial Hwy, Santa Fe Spr., CA 90670

Reason for recall

Incorrect Product Formulation: product did not contain insulin as listed in the label.

Recall Profile

Structured summary of the FDA Drug recall record
Attribute Value
Agency U.S. Food and Drug Administration
Severity class Moderate (Class II)
Status Ongoing
Recall number D-0524-2026
Date reported May 13, 2026
Date initiated December 27, 2025
Recalling firm Central Admixture Pharmacy Services, Inc (Caps) Los Angeles
Firm location Santa Fe Springs, CA
Affected scope 1 bag
Distribution CA

Profile values are sourced directly from the official FDA Drug enforcement record. Source: U.S. Food and Drug Administration.

What to do with this recall

Match your product against the recall record, then act on the agency remedy.

  • Check the recall number (D-0524-2026) and product description against the item you own. Search the archive
  • Confirm the current status with FDA Drug before acting — recall details can be updated.
  • Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next

This page summarizes the official FDA Drug record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.

Frequently Asked Questions

What product was recalled?
TPN bag (patient specific), Rx# 11-4909703-0-1, Compound Volume 1660 mL per bag, Rx only, Single Dose Injection, Refrigerated Injection, Central Admixture Pharmacy Services, Los Angeles, 13128 Imperial Hwy, Santa Fe Spr., CA 90670. Recalled by Central Admixture Pharmacy Services, Inc (Caps) Los Angeles. Units affected: 1 bag.
Why was this product recalled?
Incorrect Product Formulation: product did not contain insulin as listed in the label.
Which agency issued this recall?
This recall was issued by the FDA Drug on May 13, 2026. Severity: Moderate. Recall number: D-0524-2026.
Where was the recalled product distributed?
Distribution: CA.
How do I check if my product is affected by a recall?
Check the product description and recall number (D-0524-2026) against your product. Visit the official FDA Drug website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
Should I stop using a recalled medication or medical device?
Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.

Nearby Recalls in This Category

Other recalls in the same product category — useful for spotting patterns across the same defect class or manufacturer.

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Data Sources

Source: FDA, CPSC, and NHTSA federal recall databases. This recall: FDA Drug, reported May 13, 2026.

  • Source: FDA — Food and Drug Administration, openFDA Enforcement API (food, drug, and medical device recalls)
  • Source: CPSC — Consumer Product Safety Commission Recalls API (consumer product recalls and hazards)
  • Source: NHTSA — National Highway Traffic Safety Administration Recalls API (vehicle safety recalls)

Recall information is sourced from official federal agency databases. Always verify recall details with the issuing agency for the most current status. This information is for research and awareness purposes only.

Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records — no number is typed in by an editor. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of June 2026.