SHIMADZU RADspeed Pro recall
SHIMADZU RADspeed Pro Catalog Number: RADspeed Pro; Stationary x-ray system
Why was SHIMADZU RADspeed Pro recalled?
Cracks may occur over time on the tube holding shaft near the base of the tube mounting flange.
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?
Serial No. 0162M4501 thru 0562M45103, 3ZC5C2A0C002 thru 3ZC5C1734001, D362M42902 thru 0562M41101, 41E733E69003, MP95A8F5A001 thru MP95A9F6B001
- Product
- SHIMADZU RADspeed Pro Catalog Number: RADspeed Pro; Stationary x-ray system
- Recalling firm
- Shimadzu Medical Systems Usa Com
- Quantity
- 1673 units total
- Distribution
- Worldwide Distribution - Nationwide distribution to AK, AR, AZ, CA, CT, FL, IL, IN, KS, LA, MI, MO, NE, NJ, NM, NV, NY,OH, OK, PA, RI, SC, TN, TX, WA, WI, and Hawaii Foreign: Canada and Japan
- Recall date
- July 5, 2017
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)