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 multiple therapies across the general spectrum of clinical care. The Plum A+ family infusion pumps are self-contained, microprocessor based infusion devices.
Class I - DangerousWhat Should You Do?
- Check if you have this product: 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.
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- Report problems: Report any issues to the FDA's Safety Reporting Portal.
⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.
Recall Details
- Company:
- Hospira Inc.
- Reason for Recall:
- The fluid shield diaphragm for the Plum A+ Infusion pumps was undersized, possibly resulting in alarms and delay or interruption of therapy.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
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 multiple therapies across the general spectrum of clinical care. The Plum A+ family infusion pumps are self-contained, microprocessor based infusion devices.
Product Codes/Lot Numbers:
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.
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-2728-2016
Related Recalls
Presence of Particulate Matter: human hair found within an internal sample syringe.
Hospira, Inc. is voluntarily recalling one lot of list 14699-28, Minibore Extension Set, 59 inch with Spin Lock Collar, Non-DEHP, identified above due to a confirmed customer report of an occlusion of solvent in the male luer lock. This occlusion has the potential to prevent the set from being primed for use and cause a delay in therapy.
Failed Stability Specifications: The recalled lots did not meet the specification for color and pH throughout shelf life.