Severity
Low
LowClass IIITerminated
FDA Drug recall · Reported February 13, 2013
Ventavis (iloprost) Inhalation Solution, 10 mcg/1 mL, Sterile, 30 Single Use Ampules per carton, Manufactured for Actelion Pharmaceuticals US, Inc, 5000 Shoreline Court, Ste 200, South San Francisco, CA 94080, NDC: 66215-302-30.
Subpotent Drug: OOS (out of specification) assay result at the 12 month stability time point.
Actelion Pharmaceuticals U.S., Inc. recalled Ventavis (iloprost) Inhalation Solution, 10 mcg/1 mL, Sterile, 30 Single Use Ampules per … — a low-severity action.
Ventavis (iloprost) Inhalation Solution, 10 mcg/1 mL, Sterile, 30 Single Use Ampules per … was recalled by Actelion Pharmaceuticals U.S., Inc. in February 13, 2013. Reason: Subpotent Drug: OOS (out of specification) assay result at the 12 month stability time point.. Check the official notice for the remedy. Verify recall #D-143-2013 with the FDA Drug before acting.
The recall
Actelion Pharmaceuticals U.S., Inc. issued this low-severity FDA Drug recall — Subpotent Drug: OOS (out of specification) assay result at the 12 month stability time point..
- Low
- severity level
- Class III
- classification
- February 13, 2013
- reported
Sourced from official FDA Drug enforcement records. Verify recall #D-143-2013 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Drug action (record #D-143-2013) was formally reported on February 13, 2013, with the manufacturer initiating the action on January 16, 2013. It is classified under Low severity (Class III), with a current status of Terminated. Actelion Pharmaceuticals U.S., Inc. is listed as the recalling firm, operating out of South San Francisco, CA. Federal records list the affected scope as 3 Cartons.
The documented reason for this recall is: Subpotent Drug: OOS (out of specification) assay result at the 12 month stability time point. Distribution data in the federal record shows the product reached: CA & VA. 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
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 low severity.
Counts reflect market size and reporting activity, not inherent danger — we do not rank products by risk from raw recall volume.
Affected scope
3 Cartons
Related Recalls
6
5 from same agency
Product description
Ventavis (iloprost) Inhalation Solution, 10 mcg/1 mL, Sterile, 30 Single Use Ampules per carton, Manufactured for Actelion Pharmaceuticals US, Inc, 5000 Shoreline Court, Ste 200, South San Francisco, CA 94080, NDC: 66215-302-30.
Reason for recall
Subpotent Drug: OOS (out of specification) assay result at the 12 month stability time point.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Low (Class III) |
| Status | Terminated |
| Recall number | D-143-2013 |
| Date reported | February 13, 2013 |
| Date initiated | January 16, 2013 |
| Recalling firm | Actelion Pharmaceuticals U.S., Inc. |
| Firm location | South San Francisco, CA |
| Affected scope | 3 Cartons |
| Distribution | CA & VA |
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-143-2013) 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? ▼
Ventavis (iloprost) Inhalation Solution, 10 mcg/1 mL, Sterile, 30 Single Use Ampules per carton, Manufactured for Actelion Pharmaceuticals US, Inc, 5000 Shoreline Court, Ste 200, South San Francisco, CA 94080, NDC: 66215-302-30.. Recalled by Actelion Pharmaceuticals U.S., Inc.. Units affected: 3 Cartons.
Why was this product recalled? ▼
Subpotent Drug: OOS (out of specification) assay result at the 12 month stability time point.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on February 13, 2013. Severity: Low. Recall number: D-143-2013.
Where was the recalled product distributed? ▼
Distribution: CA & VA.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (D-143-2013) 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.
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What to do next
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Data Sources
Source: FDA, CPSC, and NHTSA federal recall databases. This recall: FDA Drug, reported February 13, 2013.
- 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.