FDARecall 99678Medicines
What to do
The FDA record of this recall has no instruction for consumers. Compare the lot codes below with your product. If they match, do not use it, and follow the notice of the firm or ask the store where you bought it. Talk to your pharmacist or doctor before stopping a medicine.Note from Recalls Watch, not agency text.
Read the official notice on accessdata.fda.gov (opens in a new tab)
Hazard
Why it was recalled
Presence of particulate matter: Particulates identified as fiberglass
FDA classification: Class I. FDA’s highest class: a reasonable probability that using the product will cause serious health consequences or death. Status: Ongoing.
Is it yours? Products and codes
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
- Lot or code
- Lot: Y495523, Y495523A, Exp 31-Oct-2027
- FDA recall number
- D-0849-2026
- Quantity
- 145,464 500mL bags
Distribution (FDA): Natonwide in the USA
About this record
- Issued by
- U.S. Food and Drug Administration
- Firm
- Baxter Healthcare Corporation (other notices of this firm)
- Title
- Composed by Recalls Watch from fields of the record; FDA records have no title.