V-TEK" recall
V-TEK", standard-countersink, cannulated, round shaft, Item Number 28.66.110
Why was V-TEK" recalled?
An investigation identified that the products were possibly manufactured from a different material than defined in the applicable specifications.
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?
All items marked with "Normed" are affected
- Product
- V-TEK", standard-countersink, cannulated, round shaft, Item Number 28.66.110
- Recalling firm
- Zimmer GmbH
- Quantity
- N/A
- Distribution
- The products were distributed to the following US states: AL, AR, AZ, CA, CO, FL, GA, HI, IA, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI, WV, and WY.
- Recall date
- May 29, 2019
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)