Baxter Issues Voluntary Nationwide Recall for Two Lots of 0.9% Sodium Chloride Injection Due to Potential Presence of Particulate Matter
Official notice
26 Aug 2026
An official FDA notice concerns Baxter. The notice reports a potential product safety risk. Do not use the product and return it as directed. Published 2026-08-26.
What to do now
Instructions for consumers are available in the official FDA notice.
Units affected
24
Official notice
2026-08-26
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Where it was sold
The source does not list specific retailers. See the official notice for where affected products were sold.
Location 1
Affected area 1
Company & contacts
Company & contacts
Brand: Baxter. Contact: Baxter International Inc.. Phone 888-229-0001, 1-800-332-1088.
Source & status
Source & status
Recall details
Recall details
Units affected
Source tier
Documents, notices & source
See the official notice and source documents for full details.
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The official notice did not include a photo. Check the product details and identifiers below.
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The official notice did not include a photo. Check the product details and identifiers below.
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The official notice did not include a photo. Check the product details and identifiers below.
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Brand match
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No image published for this recall
The official notice did not include a photo. Check the product details and identifiers below.
a product listed in the official notice - safety alert
Brand match
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Markets
Risk not stated by sourceExcel® Lactated Ringers Injection, 1000mL - safety alert
Brand match
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Markets
No image published for this recall
The official notice did not include a photo. Check the product details and identifiers below.
a product listed in the official notice - safety alert
Brand match
Medium risk
Markets
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