Centurion procedure kits labeled as: 1) BONE MARROW recall
Centurion procedure kits labeled as: 1) BONE MARROW TRAY, Pack Number SPEC0255; 2) CT/ULTRASOUND BIOPSY, Pack Number SPEC0262; 3) FINE LACERATION KIT…
Why was Centurion procedure kits labeled as: 1) BONE MARROW recalled?
Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that may pose a risk to patient health.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
SPEC0255, Lot Number 2020042080: SPEC0262, Lot Number 2018111280: SUT17215, Lot Number 2020042080: DM645, Lot Number 2018111280: DM645, Lot Number 2020042080: DM645, Lot Number 2022020780: DYNDL1159B, Lot Number 2018111280: DYNDS1064B, Lot Number 2020042080
- Product
- Centurion procedure kits labeled as: 1) BONE MARROW TRAY, Pack Number SPEC0255; 2) CT/ULTRASOUND BIOPSY, Pack Number SPEC0262; 3) FINE LACERATION KIT…
- Recalling firm
- MEDLINE INDUSTRIES, LP - Northfield
- Distribution
- worldwide
- Recall date
- September 4, 2024
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)