Rotoprone Therapy System. The Rotoprone Therapy System recall: Labeling Error
Rotoprone Therapy System. The Rotoprone Therapy System is an advanced patient care system for the treatment and prevention of pulmonary complications.
Why was Rotoprone Therapy System. The Rotoprone Therapy System recalled?
The recalled devices labeling and instructions for use contain unapproved medical claims.
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 NUMBERS: RRFK00041, RRFK00083, RRFK00232, RRFK00233, RRFK00276, RRFK00229, RRFK00215, RRFK00221, RRFK00243, RRFK00121, RRFK00263, RRFK00094, RRFK00150, RRFK00274, RRFK00103, RRFK00198, RRFK00256, RRFK00111, RRFK00290, RRFK00091, RRFK00044, RRFK00087, RRFK00241, RRFK00047, RRFK00186, RRFK00059, RRFK00170, RRFK00246, RRFK00064, RRFK00071, RRFK00289, RRFK00056, RRFK00078, RRFK00178, RRFK00051, RRFK00248, RRFK00155, RRFK00202, RRFK00247, RRFK00128, RRFK00228, RRFK00269, RRFK00126, RRFK00277, RRFK00207, RRFK00253, RRFK00067, RRFK00280, RRFK00108, RRFK00174, RRFK00161, RRFK00105, RRFK00125, RRFK00240, RRFK00052, RRFK00102, RRFK00147, RRFK00153, RRFK00082, RRFK00062, RRFK00225, RRFK00265, RRFK00070, RRFK00104, RRFK00123, RRFK00172, RRFK00085, RRFK00069, RRFK00190, RRFK00252, RRFK00287, RRFK00050, RRFK00119, RRFK00210, RRFK00239, RRFK00169, RRFK00191, RRFK00149, RRFK00168, RRFK00162, RRFK00226, RRFK00068, RRFK00284, RRFK00107, RRFK00227, RRFK00049, RRFK00166, RRFK00194, RRFK00196, RRFK00216, RRFK00148, RRFK00230, RRFK00266, RRFK00143, RRFK00097, RRFK00199, RRFK00223, RRFK00188, RRFK00101, RRFK00164, RRFK00037, RRFK00167, RRFK00192, RRFK00055, RRFK00086, RRFK00173, RRFK00177, RRFK00222, RRFK00238, RRFK00189, RRFK00038, RRFK00165, RRFK00099, RRFK00160, RRFK00141, RRFK00201, RRFK00043, RRFK00080, RRFK00112, RRFK00209, RRFK00124, RRFK00146, RRFK00042, RRFK00066, RRFK00184, RRFK00106, RRFK00224, RRFK00275, RRFK00180, RRFK00115, RRFK00251, RRFK00278, RRFK00237, RRFK00283, RRFK00219, RRFK00254, RRFK00179, RRFK00211, RRFK00127, RRFK00117, RRFK00157, RRFK00120, RRFK00073, RRFK00193, RRFK00195, RRFK00218, RRFK00096, RRFK00095, RRFK00204, RRFK00053, RRFK00282, RRFK00113, RRFK00200, RRFK00264, RRFK00118, RRFK00109, RRFK00122, RRFK00261, RRFK00244, RRFK00187, RRFK00039, RRFK00152, RRFK00181, RRFK00206, RRFK00231, RRFK00046, RRFK00093, RRFK00159, RRFK00088, RRFK00154, RRFK00076, RRFK00145, RRFK00175, RRFK00270, RRFK00065, RRFK00089, RRFK00054, RRFK00213, RRFK00040, RRFK00057, RRFK00156, RRFK00144, RRFK00249, RRFK00258, RRFK00045, RRFK00092, RRFK00176, RRFK00142, RRFK00036, RRFK00242, RRFK00151, RRFK00183, RRFK00060, RRFK00257, RRFK00061, RRFK00074, RRFK00217, RRFK00273, RRFK00171, RRFK00250, RRFK00158, RRFK00220, RRFK00163, RRFK00208, RRFK00279, RRFK00205, RRFK00098, RRFK00288, RRFK00063, RRFK00110, RRFK00072, RRFK00235, RRFK00267, RRFK00077, RRFK00079, RRFK00081, RRFK00182, RRFK00090, RRFK00197, RRFK00214, RRFK00084, RRFK00100, RRFK00245, RRFK00075, RRFK00114, RRFK00260
- Product
- Rotoprone Therapy System. The Rotoprone Therapy System is an advanced patient care system for the treatment and prevention of pulmonary complications.
- Recalling firm
- Arjo Hospital Equipment AB
- Quantity
- 226 units
- Distribution
- Worldwide Distribution. US nationwide, Germany, Austria, France, Italy, India, EU, Mexico, Switzerland, Canada, Saudi Arabia, Kuwait, Middle East, China, Japan, and Qatar.
- Recall date
- March 11, 2015
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)