Merete PediatrOS RigidTack recall
Merete PediatrOS RigidTack, REF CP20120, Size 20 mm, Sterile, Rx Only
Why was Merete PediatrOS RigidTack recalled?
Incorrect marketing label (25 mm) was applied to product size 20 mm.
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?
Model No. CP20120; Lot No. MS2117816; UDI No. (01)04048266150394(17)260706(10)MS2117816
- Product
- Merete PediatrOS RigidTack, REF CP20120, Size 20 mm, Sterile, Rx Only
- Recalling firm
- Merete Medical GmbH
- Quantity
- 26 units
- Distribution
- Domestic: Illinois; Foreign: Germany.
- Recall date
- February 23, 2022
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)