Accurian RF Ablation recall
Accurian RF Ablation, Cannula pk, Accurian, 150mm, 20G, 10mm, CS Product Number: AC0012 GTIN / UPN: 20763000153629 - Product Usage: (sterile…
Why was Accurian RF Ablation recalled?
Insertion difficulty of the probes. The probe was catching on a lip inside the hub of the cannula.
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 # BY19L009 BY20A012
- Product
- Accurian RF Ablation, Cannula pk, Accurian, 150mm, 20G, 10mm, CS Product Number: AC0012 GTIN / UPN: 20763000153629 - Product Usage: (sterile…
- Recalling firm
- Medtronic Sofamor Danek USA Inc
- Quantity
- 352 pk
- Distribution
- Worldwide distribution - US Nationwide distribution and the countries of Belgium and Australia.
- Recall date
- July 29, 2020
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)