Maquet Getinge Group Pediatric Arterial Cannula Maquet recall
Maquet Getinge Group Pediatric Arterial Cannula Maquet Cardiopulmonary AG Kehler Strabe 31 76437 Rastatt Germany Phone +49 7222 932-0 Fax: +49 7222…
Why was Maquet Getinge Group Pediatric Arterial Cannula Maquet recalled?
Certain pediatric arterial cannulas may have limited flexibility due to an increased length of the "hardened" cannula tip.
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?
510k023251 US Catalog Number 161412 Batch Number 92048923 Foreign Catalog number 161412 Batch number 92048923 Catalog number 161412 Batch number 92051578
- Product
- Maquet Getinge Group Pediatric Arterial Cannula Maquet Cardiopulmonary AG Kehler Strabe 31 76437 Rastatt Germany Phone +49 7222 932-0 Fax: +49 7222…
- Recalling firm
- Maquet Inc.
- Quantity
- 20 devices US; 122 devices foreign
- Distribution
- Worldwide Distribution - USA including MI, MN and Internationally
- Recall date
- August 22, 2012
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)