B-K Medical A/S recalls Ultrasound System 1300
Reason for recall
GE HealthCare has become aware that the Instructions for Use within the user guide and service manual do not adequately state the required battery replacement intervals, end-of-life handling procedures, or general battery safety precautions.
Affected product
Check your device
Enter a lot, serial, REF, or UDI number from your device's label to check it against this recall's listed codes.
Ultrasound System 1300, bkSpecto w/battery; Model No. 1300-21 or 1300-S1; System, Imaging, Pulsed Doppler, Ultrasonic
Lot / code information
- GTIN
- 05704916001285 and pending
- Serial #
2002690, 2008466, 2008495, 2006774, 5012683, 5013881 — +1474 moreShow all
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2006678, 5011821, 2003499, 2003560, 2003583, 2003617, 2008485, 2003821, 2001458, 2001481, 2001485, 2001487, 2008741, 2006113, 2002589, 5016317, 2008140, 2001645, 2006309, 2006369, 2006458, 2006475, 2006561, 2006566, 2006595, 2006620, 2006778, 2006934, 2006997, 2007167, 2007526, 2007558, 2006987, 2007036, 2008039, 2008161, 2008235, 2009248, 2005330, 2008713, 2003486, 2004191, 2002184, 5015355, 2005731, 5013279, 2005500, 2005825, 2006261, 2005414, 2003492, 2008050, 5014818, 5016302, 2007268, 5015712, 5015711, 5015917, 2008694, 2000822, 2008536, 5011820, 5012317, 2002789, 2008679, 5015411, 5015441, 5015918, 2001695, 2006249, 2001171, 2001936, 2002714, 2007281, 2004128, 5016458, 5012783, 2009187, 5012312, 2001861, 2007305, 2009077, 2008502, 2008743, 2003677, 2003667, 2003747, 5012957, 2005322, 2004982, 2005009, 2007270, 2002420, 2008045, 5012970, 5016090, 2002825, 2006147, 5014510, 5015910, 2008379, 2007808, 5013655, 2008143, 2008201, 5012565, 2002135, 2002150, 2002151, 2002152, 2001426, 2008375, 5013887, 2003630, 2008145, 5011467, 2008279, 2003797, 2006525, 2002575, 2004249, 2003624, 2007032, 2006318, 5013459, 5013886, 2003626, 2003399, 2005277, 2005248, 2008389, 2007627, 5015205, 5015208, 2008708, 2008977, 2008160, 5012960, 5014277, 2008726, 2001843, 2006313, 2007313, 5013463, 2008681, 5016201, 5014919, 5014335, 5016080, 2003355, 2003510, 5013890, 5013132, 5012955, 2001758, 2008246, 2008265, 2007061, 5012051, 2007614, 5012785, 2005638, 2008717, 2008518, 2006672, 2001031, 5014921, 2002458, 5015024, 5011485, 2008899, 2006496, 2006521, 2008061, 5013871, 2006107, 2002813, 2004293, 5015216, 2008387, 2008154, 5012546, 5012548, 5014332, 2008200, 2006230, 2003006, 5016086, 2002143, 2006247, 2002341, 2002889, 2009107, 5012539, 2005517, 2007004, 5015715, 2004375, 2002862, 5011458, 2008253, 2008459, 2008487, 2008493, 2008512, 2008516, 2008524, 5015913, 2005531, 2005537, 2005332, 2003754, 2004647, 2005417, 2004374, 2003612, 2003794, 2007178, 2004203, 2006495, 2007018, 2006998, 2006787, 2007173, 5015716, 2004243, 2002846, 2006862, 2002394, 2002414, 2002885, 2003410, 2003449, 2006215, 2003446, 2003467, 2006860, 5015025, 5013283, 2002332, 2003445, 2003057, 2005528, 2005534, 2001766, 2006132, 2004386, 2003448, 2003179, 2002140, 2004435, 2006661, 2001651, 2006278, 2000712, 5012791, 2003581, 5014801, 5014802, 2001137, 2002051, 2000780, 2002047, 5014136, 5014269, 5014822, 2001701, 2001713, 2001783, 2002338, 5014216, 2008083, 2008125, 2008156, 2008511, 2008734, 2008779, 2009157, 5011483, 2007748, 5011484, 2006988, 2003468, 2000403, 2001084, 2001086, 5014138, 5015446, 2000771, 2006411, 2000281, 2000479, 2000785, 2000248, 5014527, 2000322, 2004287, 2004260, 2002783, 5015444, 5013130, 5012402, 2000164, 5014215, 2005751, 2000577, 2003614, 2007273, 5016077, 5016078, 2002048, 2003586, 2005364, 2001297, 2005755, 2007680, 2004455, 2000467, 5014814, 5014816, 5011161, 2005396, 5014912, 5015699, 2000828, 2001688, 5011812, 5011824, 5015657, 5014140, 5014808, 5014807, 2000504, 200381 …- Serial #
2007274, 2001754, 2003771, 2003611, 2005842, 2007514 — +211 moreShow all
2007274, 2001754, 2003771, 2003611, 2005842, 2007514, 2004986, 2003773, 2006652, 2006072, 2005329, 2006408, 2005728, 2003239, 2002206, 2006085, 2005444, 2002946, 2005987, 2006453, 5014797, 2006768, 2006876, 2007053, 5016019, 2003453, 2004206, 2004197, 2001387, 2006265, 2003746, 5015897, 2002715, 5016202, 2003656, 2002551, 2007115, 5015916, 2007564, 2001024, 2004362, 2004577, 2002911, 2001922, 2005628, 2005856, 2002860, 2003750, 2006212, 2002945, 2005670, 2002340, 2007676, 2004148, 2003116, 2001822, 5015641, 5016006, 2007141, 2005339, 2003398, 2006066, 2006580, 2003330, 2006228, 2003198, 2001025, 2003579, 2001690, 5015332, 2004299, 2004144, 2007049, 2005190, 2001788, 2002809, 2000921, 2000997, 2001010, 5015643, 5016471, 5016475, 2005532, 2004157, 2006367, 2005840, 2003829, 2007556, 2003412, 2006875, 2004168, 2001300, 2004985, 2005608, 2005837, 2006933, 2002045, 2006589, 2003718, 2007179, 2007687, 2005803, 2005421, 2002803, 2005729, 2002893, 2004271, 2003815, 5016020, 2006666, 2007317, 2004156, 5015340, 2002287, 5015345, 2003118, 2002018, 2002452, 5015719, 5016455, 2002455, 2003689, 2005584, 2002812, 2001937, 2001931, 2003549, 2004142, 2006451, 5015718, 2003680, 2007682, 2001867, 2007068, 2006473, 2003688, 2001170, 2001304, 2005469, 2002613, 2005394, 2006523, 2002879, 5014902, 5016190, 2006204, 2003244, 2001679, 2002148, 5016000, 2004252, 2004460, 5016084, 2001866, 2003762, 2003822, 5015460, 2001752, 5015854, 5015999, 2001827, 2001855, 2005747, 2003678, 2001149, 2001151, 5015334, 5015335, 5015336, 5015706, 5015707, 5016304, 5016210, 2007090, 5013127, 2001784, 2001707, 2001851, 2003748, 2006255, 2005630, 2006201, 2006226, 2005219, 2005485, 2003485, 2006202, 2002147, 2001524, 2002149, 2005617, 2005667, 2005718, 2003484, 2006809, 2002453, 2004253, 5016191, 5016203, 2004279, 2001308, 5015997, 2006643, 2004383, 2004457, 2004536, 2004608, 2004634, 2004635, 2004637, 2004785, 2004796, 2004797, 2004931, 2004946, 2004952, 5015874
What the firm is doing
GE Healthcare issued an "URGENT MEDICAL DEVICE CORRECTION NOTICE" to its consignees on 10/09/2025 via traceable means. The notice explained the issue, potential risk, and requested: "Actions to be taken by Customer / User You can continue to use your device by following the instructions below: 1. Review and follow the applicable addendums to the Instructions for Use and the updated Service Manuals. The Addendums and Service Manuals are available for download at: https://www.gehealthcare.com/support/manuals. 2. Follow the conditions defined within the addendum and Service Manual applicable to your product for further instructions. 3. Place the applicable addendum and Service Manual with your existing product Instructions for Use. 4. If you have difficulty accessing the documentation or require a printed copy of the applicable addendum or Service Manual, please contact a GE HealthCare Service Representative for assistance. Please ensure all potential users in your facility are made aware of this safety notification and the required actions. Please retain this document for your records." For questions or concerns regarding this notification, please contact GE HealthCare at 1-800-645-4442 or bksupport.us@gehealthcare.com or your local Service Representative.
DistributionShow detailsHide
Worldwide distribution: US (nationwide) and OUS (foreign) to countries of: Algeria, Argentina, Australia, Austria, Belgium, Brazil, Bulgaria, Canada, Chile, China, Colombia, Costa Rica, Croatia, Czech Republic, Denmark, Dominican Rep, Ecuador, Estonia, Finland, France, Georgia, Germany, Greece, Hong Kong, Hungary, Iceland, India, Indonesia, Ireland, Israel, Italy, Japan, Korea (Republic Of), Kuwait, Latvia, Lebanon, Luxembourg, Malaysia, Mexico, Mongolia, Morocco, Nepal, Netherlands, New Zealand, Norway, Pakistan, Panama, Peru, Philippines, Poland, Portugal, Qatar, Romania, Russia, Saudi Arabia, Serbia, Singapore, Slovakia, Slovenia, South Africa, Spain, Sweden, Switzerland, Taiwan, Thailand, Turkiye, Ukraine, United Arab Emirates, and United Kingdom.
Use of the product may cause temporary or medically reversible adverse health consequences.
Sources & references
- FDA enforcement recordOfficial FDA database entry for Z-0436-2026
- FDA 510(k) clearance · K231764The device's official FDA premarket clearance record
- FDA device classification · IYNOfficial FDA classification for this device type
- CFR regulation · 21 CFR 892.1550The federal regulation governing this device
- FDA recall announcementSearch FDA.gov for the official press announcement
- Find B-K Medical A/SSearch for the manufacturer's official notice
- News coverageRecent reporting on this recall and manufacturer
- openFDA data recordThe raw JSON record this page is built from
Source: U.S. FDA openFDA device enforcement reports. This summary is informational and may lag or differ from the official record. Always verify against the FDA before acting.
Taylor Coteus is RecallWatch's Legal News Analyst, covering FDA medical-device enforcement and patient-safety litigation. He reviews every recall against the FDA's official openFDA record before it is published and is responsible for corrections and editorial accuracy.
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