SLIM Handle recall
SLIM Handle - catalogue #: SLM-HND100 a component of Simple Locking Intramedullary (SLIM) System
Why was SLIM Handle recalled?
Handle could jam with the Driver due to the detachment of an internal Connector Ring.
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 # 150115-09, 160427-01 and A162-02
- Product
- SLIM Handle - catalogue #: SLM-HND100 a component of Simple Locking Intramedullary (SLIM) System
- Recalling firm
- Pega Medical Inc.
- Quantity
- 19
- Distribution
- CA, DE, FL, IL, NC, NE, NY and TN
- Recall date
- August 21, 2019
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)