Monoject Blunt Cannula recall: Sterility Concern
Monoject Blunt Cannula, 20 G x 1-1/2" (0.902 mm x 3.8 cm) Item code: 8881202363
Why was Monoject Blunt Cannula recalled?
Manufacturing defect was found for the cartridge component, which could compromise the sterility barrier of the product
What should I do if I have this product?
Review the official FDA enforcement record for current 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?
Lot Number: 907734
- Product
- Monoject Blunt Cannula, 20 G x 1-1/2" (0.902 mm x 3.8 cm) Item code: 8881202363
- Recalling firm
- Cardinal Health 200, LLC
- Quantity
- N/A
- Distribution
- Nationwide Foreign: AU, BE, CA, DK, FI, GB, IE, NL
- Recall date
- July 31, 2019
- Classification
- Class II
- Status
- Completed
- Agency
- FDA (device)