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Presence of particulate matter: Particulates identified as fiberglass
- Agency
- FDA Drug
- Recall date
- Aug 17, 2026
- Status
- Ongoing
- Company
- Baxter Healthcare Corporation
1. What product was recalled?
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0.9% Sodium Chloride Injection USP 500 mL, VIAFLEX Plastic Containers, with 24 units per case. Baxter Healthcare Corporation, Deerfield, IL, 60015, USA, Made in USA, NDC 0338-0049-03
Quantity: 145,464 500mL bags
Code or lot text: Lot: Y495523, Y495523A, Exp 31-Oct-2027
- LOT
- Exp 31-Oct-2027
- LOT
- Lot: Y495523
- LOT
- Y495523A
- NDC
- 0338-0043
- NDC
- 0338-0043-03
- NDC
- 0338-0043-04
- NDC
- 0338-0049
- NDC
- 0338-0049-01
- NDC
- 0338-0049-02
- NDC
- 0338-0049-03
- NDC
- 0338-0049-04
- NDC
- 0338-0049-10
- NDC
- 0338-0049-11
- NDC
- 0338-0049-18
- NDC
- 0338-0049-31
- NDC
- 0338-0049-38
- NDC
- 0338-0049-41
- NDC
- 0338-0049-48
- RECALL-NUMBER
- D-0849-2026
2. Is my exact product affected?
Compare every printed identifier. A matching value can indicate that your product is included.
3. What is the hazard?
Presence of particulate matter: Particulates identified as fiberglass
4. What should I do now?
Follow the FDA recall notice and contact the recalling company for current instructions.
5. Where was it sold or distributed?
Natonwide in the USA
6. Were injuries or illnesses reported?
No separate injury or illness statement was present in the normalized record. Check the official source for the latest report.
7. What remedy is available?
Follow the FDA recall notice and contact the recalling company for current instructions.
8. Is the recall active or closed?
The source status is Ongoing. The Recall Guy's urgency label is urgent, which is a separate deterministic site label.
9. When was the information checked?
Last checked .
- created
10. Where is the official source?
Open the official FDA Drug source
The Recall Guy normalizes public source data for easier checking. Source agencies remain authoritative. Confirm identifiers and instructions at the official source.