Portex Anaerobic Pulsator Arterial Blood Sampling Kit recall
Portex Anaerobic Pulsator Arterial Blood Sampling Kit, with Liquid Sodium Heparin for Gases and Electrolytes. Reorder Number: G1392 Product Usage: The…
Why was Portex Anaerobic Pulsator Arterial Blood Sampling Kit recalled?
The outer box label is marked with the correct expiration date of 08/2016. The inner Tyvek Unit Label is marked with 08-2017 which exceeds the actual expiration date by one year.
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: 2782094
- Product
- Portex Anaerobic Pulsator Arterial Blood Sampling Kit, with Liquid Sodium Heparin for Gases and Electrolytes. Reorder Number: G1392 Product Usage: The…
- Recalling firm
- Smiths Medical ASD, Inc.
- Quantity
- 900 units
- Distribution
- US in the state of FL.
- Recall date
- February 4, 2015
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (device)