Greenwich Glutathione Injection
OFFICIAL-SOURCE RECALL · UNITED STATES
B. Braun 0.9% Sodium Chloride Injection USP, 100 mL, in a 150 mL PAB® Recall: Presence of particulate matter
Use the identifiers printed on your item to determine whether this recall may affect the product you own.
CountryUnited StatesPublishedSeptember 3, 2026Last updatedSeptember 3, 2026Official source last checkedSeptember 4, 2026 at 8:16 PM UTC
CHECK THE ITEM YOU OWN
Is your product affected?
- Brand
- B. Braun
- Product
- 0.9% Sodium Chloride Injection USP, 100 mL, in a 150 mL PAB® Container
- Manufacturer
- B. Braun Medical Inc.
- NDC
- 0264-180032
- Lot number
- J6B435
- Expiration date
- 30APR2027
- Package size
- 100 mL, 150 mL
The barcode may identify the product type, while the recall may apply only to certain lots, dates or variants. Check all identifiers listed in the official recall.
Why this product was recalled
Presence of particulate matter identified as iron oxide
Hazard
Presence of particulate matter identified as iron oxide
What consumers should do
Consumers with questions regarding this recall can contact B. Braun by emailing recalls@bbraunusa.com, Monday to Friday 8:00am to 5:00pm EST. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product. Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax.
Official recall notice
B. Braun Medical Inc. Issues Voluntary Nationwide Recall of 0.9% Sodium Chloride Injection USP, 100 mL, in a 150 mL PAB® Container Due to the Presence of Particulate Matter
Agency: U.S. Food & Drug Administration
Official publication date: September 3, 2026
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