Pinnacle¿ Destination¿ Peripheral Guiding Sheath recall
Pinnacle¿ Destination¿ Peripheral Guiding Sheath, 8 French, 90cm, Straight Tip, Cross Cut Valve. Acts as a conduit to facilitate the introduction of…
Why was Pinnacle¿ Destination¿ Peripheral Guiding Sheath recalled?
Medical devices were incorrectly labeled with extended expiration dates.
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 MM27
- Product
- Pinnacle¿ Destination¿ Peripheral Guiding Sheath, 8 French, 90cm, Straight Tip, Cross Cut Valve. Acts as a conduit to facilitate the introduction of…
- Recalling firm
- Terumo Medical Corporation
- Quantity
- 20 units
- Distribution
- Nationwide Distribution.
- Recall date
- July 3, 2013
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)