Philips Ultrasound recall
Philips Ultrasound, Model Q-Station, with software version 3 or higher, Catalog number: 795088; Part Number: 989605382391 Q-Station is application…
Why was Philips Ultrasound recalled?
Philips Healthcare has discovered a problem in the Philips Ultrasound Q-Station version 3.0 or higher that could result in measurements from a study (Structured Report) to be appended to subsequent studies for other patients.
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?
*****************US Serial numbers***************************************** 2176-IAF08E60-15D4, 2187-VAC5T6CD-157D, 2C98-25A23E3A-4B2E, 34F5-4084F543-80EA, 3A5D-4079F60B-80D4, 54B0-HADF24F2-15B1, 678B-NAE42F41-15BB, 6FF9-259B5EB7-4B20, 725B-GACE30D1-158F, 72EE-408914F8-80F2, 7A39-497627F7-92C9, 8536-IAD33B20-1599, A584-QAE84EF6-15C3, A838-IAE2CF5A-15B8, B903-407CB5D9-80D9, BDC7-TAE25A0D-15B7, D356-YAE1E4C0-15B6, D60A-GADC6524-15AB, D8BE-KAD6E588-15A0, DB72-RAD165EC-1595, DE26-WACBE650-158A, E0DA-XAC666B4-157F, E16D-40814ADB-80E2, E8E5-TAE16F73-15B5, EE4D-IAD6703B-159F, F669-PAC5F167-157E, F90C-MAEBF95E-15CA, H944-VACAFBB6-1589, MBF8-WAC57C1A-157E, U9D7-4085DFDD-80EC. ********************Serial numbers in CANADA**************************************** 1ED3-QACA8669-1588, 4489-SAD49B07-159C, B054-UAD25086-1597, C897-TACC5B9D-158B, and F3B5-IACB7103-1589. *********************Serial numbers in other countries*********************************** 114F-QAE6M475-15BF, 11F3-40756109-80CB, 16B7-KADBT53D-15A9, 196B-UAD585A1-159E, 1F66-40856A90-80EB, 221A-407FEAF4-80E0, 23FD-4977FD2B-92CD, 242A-MAEBPEC4-15C9, 24CE-407A6B58-80D5, 2782-4074EBBC-80CA, 2965-496CFDF3-92B7, 29E4-25A7BDD6-4B39, 2C46-QADA8FF0-15A8, 2EFA-RAD51054-159D, 2F4C-259CBE9E-4B23, 3716-IAC49180-157C, 37A9-407F75A7-80DF, 3C6D-XAE519DB-15BD, 3CBF-25ACC825-4B43, 3D11-4074766F-80C9, 41D5-NADA1AA3-15A7, 47D0-4089FF92-80F4, 49F1-IAC99BCF-1586, 4C94-YAEFA3C6-15D2, 4CA5-UAC41C33-157B, 4F1B-49771291-92CB, 4FEC-407980BE-80D3, 524E-25AC52D8-4B42, 5764-MAD9A556-15A6, 5A18-QAD425BA-159B, 5CCC-HACEA61E-1590, 5F80-MAC92682-1585, 6013-4084IAA9-80E8, 61F6-497C1CE0-92D5, 62C7-407E8B0D-80DD, 657B-4079TB71-80D2, 6CF3-WAD93009-15A5, 750F-TAC8B135-1584, 75A2-4083955C-80E7, 7856-407E15C0-80DC, 7B0A-40789624-80D1, 7CED-4970A85B-92BE, 7D6C-25AB683E-4B40, 7FCE-HADE3A58-15AF, 8282-JAD8BABC-15A4, 87EA-PACDBB84-158E, 8A9E-RAC83BE8-1583, 8B31-4083200F-80E6, 8D14-497B3246-92D3, 8D41-NAEE43DF-15CF, 8DE5-407DA073-80DB, 8FF5-NAE8C443-15C4, 9099-407820D7-80D0, 9811-WAD8456F-15A3, 9D79-WACD4637-158D, A0C0-4082AAC2-80E5, A374-407D2B26-80DA, A628-4077AB8A-80CF, A80B-496FBDC1-92BC, AAEC-MADD4FBE-15AD, ADA0-PAD7D022-15A2, B308-JACCD0EA-158C, B39B-4087B511-80EF, B5BC-RAC7514E-1581, B64F-40823575-80E4, B832-497A47AC-92D1, B85F-UAED5945-15CD, BAE6-4974C810-92C6, BBB7-4077363D-80CE, BE19-25AAH857-4B3D, C07B-KADCDA71-15AC, CBDE-4081C028-80E3, CDC1-4979D25F-92D0, CE92-407C408C-80D8, D146-4076C0F0-80CD, E37D-JAEC6EAB-15CB, E421-407BCB3F-80D7, F448-4086552A-80EC, F6FC-4080D58E-80E1, F8DF-4978E7C5-92CE, F9B0-407B55F2-80D6, FC64-4075D656-80CB, T3DC-SAD5FAEE-159F, TF3F-407AE0A5-80D6, VC8B-40806041-80E1, and Y690-GAD07B52-1594. **********NEWLY ADDED FOUR AFFECTED SERIAL NUMBERS******* aaec-madd4fbe-15ad; WE9B-QAEB8411-15CA; 2B14-MDE9A2F9-1BC6; and 3C40-4972P842-92C1
- Product
- Philips Ultrasound, Model Q-Station, with software version 3 or higher, Catalog number: 795088; Part Number: 989605382391 Q-Station is application…
- Recalling firm
- Philips Ultrasound, Inc.
- Quantity
- 125 units (30 in US and 95 international)
- Distribution
- Worldwide Distribution - US (nationwide) and Puerto Rico; internationally to Australia, Canada, Colombia, France, Germany, Great Britain, India, Italy, Mexico, Netherlands, Norway, Pakistan, Poland, Russia, Singapore, Spain, Switzerland, Thailand, and Zimbabwe.
- Recall date
- June 24, 2015
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)