List No. 14210-28 recall
List No. 14210-28; PLUM BLOOD SET; 100 mL Burette with Prepierced Injection Site, 170 Micron Filter, Prepierced Port, Non-Vented, 105 Inch, Non-DEHP…
Why was List No. 14210-28 recalled?
It was discovered that there was a potential for the piercing pin on certain Hospira blood sets to puncture the outer wall of blood bags during insertion of the pin into the blood bag.
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?
List Number: 14210-28; Lot Number: 053835H
- Product
- List No. 14210-28; PLUM BLOOD SET; 100 mL Burette with Prepierced Injection Site, 170 Micron Filter, Prepierced Port, Non-Vented, 105 Inch, Non-DEHP…
- Recalling firm
- Hospira Inc.
- Quantity
- 96 units
- Distribution
- Worldwide Distribution - USA (nationwide) and Puerto Rico and Internationally to Costa Rica.
- Recall date
- August 14, 2013
- Classification
- Class I
- Status
- Terminated
- Agency
- FDA (device)