Abbott Laboratories Gemstar Therapy Pain Management I. V. Infusion Pump, List #: 13150-04; 2.9 Software Version Recall
Hazard assessment based on recall description.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Gemstar Therapy Pain Management I. V. Infusion Pump, List #: 13150-04; 2.9 Software Version
Brand
Abbott Laboratories
Lot Codes / Batch Numbers
All serial numbers
Products Sold
All serial numbers
Abbott Laboratories is recalling Gemstar Therapy Pain Management I. V. Infusion Pump, List #: 13150-04; 2.9 Software Version due to Products contain software deficiencies which could allow over infusion thereby administering excess medication.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Products contain software deficiencies which could allow over infusion thereby administering excess medication.
Recommended Action
Per FDA guidance
On 4/1/03, the firm issued letters via Federal Express Overnight Delivery to all its direct consignees, informing them of the affected devices and providing instructions on the recall.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026