Stryker PROFESS Registration Kit. The Stryker PROFESS recall
Stryker PROFESS Registration Kit. The Stryker PROFESS Registration Kit is a member of the Navigation portfolio and is used as an intraoperative…
Why was Stryker PROFESS Registration Kit. The Stryker PROFESS recalled?
Product shipped proximate to or past the expiration date listed on the product label.
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 #202085 Stryker Product Number: 6001-420-000
- Product
- Stryker PROFESS Registration Kit. The Stryker PROFESS Registration Kit is a member of the Navigation portfolio and is used as an intraoperative…
- Recalling firm
- Stryker Instruments Div. of Stryker Corporation
- Quantity
- 65
- Distribution
- US (nationwide) Distribution to the states of : CA, CT, GA, IL, IN, MA, MD, NC, OH, PA, TN, and TX.
- Recall date
- May 17, 2017
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)