OFFICIAL-SOURCE RECALL · UNITED STATES
BD for Specific Lots of BD® Intraosseous Vascular Access System Recall: FDA Intergovernmental Affairs Digest
Use the identifiers printed on your item to determine whether this recall may affect the product you own.
CountryUnited StatesPublishedAugust 7, 2026Last updatedAugust 7, 2026Official source last checkedAugust 9, 2026 at 7:02 PM UTC
CHECK THE ITEM YOU OWN
Is your product affected?
- Brand
- See official notice
- Product
- BD Issues Nationwide Recall for Specific Lots of BD® Intraosseous Vascular Access System Needle Sets Due to Reports of Difficulty Removing the Obturator
- Manufacturer
- See official notice
- Model number
- ing
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
FDA
Hazard
FDA
Official recall notice
BD Issues Nationwide Recall for Specific Lots of BD® Intraosseous Vascular Access System Needle Sets Due to Reports of Difficulty Removing the Obturator
Agency: U.S. Food & Drug Administration
Official publication date: August 7, 2026
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