ProCuity bed series recall
ProCuity bed series, model number 3009, item number: 3009PX-L-200
Why was ProCuity bed series recalled?
Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA 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?
UDI-DI (GTIN): 07613327541199 Serial numbers: 2211000305 , 2112000828 , 2109001676 , 2109001666 , 2209002657 , 2208001565 , 2208001555 , 2208001541 , 2203002178 , 2203002161 , 2203002159 , 2203002157 , 2106000232 , 2106000210
- Product
- ProCuity bed series, model number 3009, item number: 3009PX-L-200
- Recalling firm
- Stryker Medical Division of Stryker Corporation
- Distribution
- Distribution US Nationwide including Puerto Rico, Australia, Canada, Chile, China, Mexico, Poland, Spain and Switzerland.
- Recall date
- December 13, 2023
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)