Plum A+3 Infusion Pump System. List Number 12348. The recall
Plum A+3 Infusion Pump System. List Number 12348. The Plum A+ Infusion Systems are a multi-purpose family of devices that provides precise delivery of…
Why was Plum A+3 Infusion Pump System. List Number 12348. The recalled?
The fluid shield diaphragm for the Plum A+ Infusion pumps was undersized, possibly resulting in alarms and delay or interruption of therapy.
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?
List number 12348, Serial Numbers: 13740156, 13740256, 13740266, 13740351, 13740380, 13740451, 13740508, 13740612, 13740632, 13740731, 13740732, 13740733, 13740734, 13740735, 13740736, 13740737, 13740738, 13740739, 13740740, 13740741, 13740742, 13740743, 13740744, 13740745, 13740746, 13740747, 13740748, 13740749, 13740750, 13740751, 13740752, 13740753, 13740754, 13740755, 13740756, 13740757, 13740758, 13740759, 13740760, 13740761, 13740762, 13740763, 13740764, 13740765, 13740766, 13740767, 13740768, 13740769, 13740770, 13740771, 13740772, 13740773, 13740774, 13740775, 13740776, 13740777, 13740778, 13740779, 13740780, 13740781, 13740782, 13740783, 13740784, 13740785, 13740786, 13740787, 13740788, 13740789, 13740790, 13740791, 13740792, 13740793, 13740794, 13740795, 13740796, 13740797, 13740798, 13740799, 13740800, 13740801, 13740802, 13740803, 13740804, 13740805, 13740806, 13740807, 13740808, 13740809, 13740810, 13740811, 13740812, 13740813, 13740814, 13740815, 13740816, 13740818, 13740819, 13740820, 13740821, 13740822, 13740823, 13740824, 13740825, 13740826, 13740827, 13740828, 13740829, 13740830, 13740831, 13740832, 13740833, 13740834, 13740835, 13740836, 13740837, 13740838, 13740839, 13740840, 13740841, 13740842, 13740843, 13740844, 13740845, 13740846, 13740847, 13740848, 13740849, 13740850, 13740851, 13740852, 13740853, 13740854, 13740855, 13740856, 13740857, 13740858, 13740859, 13740860, 13740861, 13740862, 13740863, 13740864, 13740865, 13740866, 13740867, 13740868, 13740869, 13740870, 13740871, 13740872, 13740873, 13740874, 13740875, 13740876, 13740877, 13740878, 13740879, 13740880, 13740881, 13740882, 13740883, 13740884, 13740885, 13740886, 13740887, 13740888, 13740889, 13740890, 13740891, 13740892, 13740893, 13740894, 13740895, 13740896, 13740897, 13740898, 13740899, 13740900, 13740901, 13740902, 13740903, 13740904, 13740905, 13740906, 13740907, 13740908, 13740909, 13740910, 13740911, 13740912, 13740913, 13740914, 13740915, 13740916, 13740917, 13740918, 13740919, 13740920, 13740921, 13740922, 13740923, 13740924, 13740925, 13740926, 13740927, 13740928, 13740929, 13740930, 13740977, 13740980, 13740982, 13740986, 13740994, 13741025.
- Product
- Plum A+3 Infusion Pump System. List Number 12348. The Plum A+ Infusion Systems are a multi-purpose family of devices that provides precise delivery of…
- Recalling firm
- Hospira Inc.
- Quantity
- 357,778 total
- Distribution
- United States nationwide distribution including PR, and USVI. Costa Rica, Turks and Caicos, and Dominican Republic.
- Recall date
- September 14, 2016
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)