Baxter Healthcare Corporation Duo-Vent Solution Set Recall
FDA recall of Baxter Duo-Vent Solution Set and Male Luer Lock Adapter (Product Code 1C8507; Solution Administration Sets) due to reports of air bubbles in the drip chamber and tubing when a pressure cuff is in use or when the tubing is flushed at the fully open position. About 24,528 units distributed nationwide in the United States are affected; the affected lots are DR26C27062 (exp 30-MAR-2028), DR26D14031 (exp 15-APR-2028), and DR26E13055 (exp 14-MAY-2028).
| Brand | Baxter Healthcare Corporation |
|---|---|
| Product | Baxter Duo-Vent Solution Set and Male Luer Lock Adapter, Product Code 1C8507; Solution Administration Sets |
| Reason | Baxter received customer reports of air bubbles in the drip chamber and tubing when a pressure cuff is in use or when the tubing is flushed at the fully open position. |
| Severity | critical |
| Units affected | 24528 units |
| Distribution | US Nationwide. No OUS consignees. |
| Agency | FDA |
WHAT YOU SHOULD DO
- Do not use affected Baxter Duo-Vent solution sets or adapters.
- Check if your device lot number matches DR26C27062, DR26D14031, or DR26E13055.
- Contact your healthcare provider or Baxter for replacement/return instructions.
- Follow any recall-specific instructions provided by the FDA.
How to identify the recalled item
| Lot / date codes | UDI/DI 00085412014319, Lot Numbers: DR26C27062, exp. 30-MAR-2028; DR26D14031, exp. 15-Apr-2028; DR26E13055, exp. 14-May-2028 |
|---|---|
| Lot / date codes | Lot # LD175708, Exp Date: 14-Feb-2027. |
These are the identifiers FDA published for this recall. Most recall notices list no UPC or model number at all — if the code on your item is not shown here, that does not mean the item is excluded. Check the official notice, or contact the company.
Other Baxter Healthcare Corporation recalls
This is an automatically maintained record of an official recall notice. Details can change; always follow the official notice linked above. See all records in the Recall Database.