CLASS II Device recall · Reported 5 May 2021 · FDA Enforcement Report
Spectrum IQ - Infusion Pump recalled by Baxter Healthcare
Baxter Healthcare is recalling Spectrum IQ - Infusion Pump, distributed nationwide in the US. The recall was initiated on 19 Mar 2021 and the FDA has classified it as Class II.
Check your package
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
Recall details
- Recall number
- Z-1487-2021
- FDA event ID
- 87568
- Recalling firm
- Baxter Healthcare, Medina, NY
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 19 Mar 2021
- FDA classified
- 23 Apr 2021
- Reported
- 5 May 2021
- Type
- Voluntary: Firm initiated
- Customers notified by
- N/A
- Reason category
- Device Malfunction
- Device type
- Infusion Pumps
Timeline
| 19 Mar 2021 | Recall initiated by company | |
| 23 Apr 2021 | Classified by FDA | +35 days |
| 5 May 2021 | Published in enforcement report | +12 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Potentially defective component in the AC power adapter which may fail over time.
Device recalls are issued when a component, software or design fault could cause the device to fail or give wrong readings. Many are corrections applied in the field rather than physical returns.
Product as listed by the FDA
Spectrum IQ - Infusion Pump - Product Usage: intended to be used for the controlled administration of fluids.
Where it was distributed
Worldwide distribution - US Nationwide distribution in the states of AL, AR, CA, CT, FL, IA, IN, LA, MA, MD, ME, MN, MO, MS, MT, NC, NJ, NY, OH, PA, RI, SC, TN, TX and the country of Puerto Rico.
Nationwide AlabamaArkansasCaliforniaConnecticutFloridaIowaIndianaLouisianaMassachusettsMarylandMaineMinnesotaMissouriMississippiMontanaNorth CarolinaNew JerseyNew YorkOhioPennsylvania
Questions about this recall
Why was it recalled?
Potentially defective component in the AC power adapter which may fail over time.
Which lots are affected?
Product Code: 3570009 Serial Numbers: 3008222, 3539596, 3546215, 3586366, 3619652, 3622541, 3623709, 3624381, 3624740, 3625247, 3011477, 3539777, 3547110, 3586582, 3619759, 3622688, 3623721, 3624383, 3624744, 3625266, 3012363, 3540327, 3547708, 3586798, 3619767, 3622691, 3623728, 3624393, 3624749, 3625275, 3013708, 3540486, 3548756, 3587371, 3620063, 3622721, 3623737, 3624396, 3624761, 3625300, 3014132, 3541062, 3549098, 3587774, 3620333, 3622773, 3623754, 3624409, 3624763, 3625308, 3014459, 3541163, 3552089, 3588483, 3620532, 3622779, 3623789, 3624414, 3624777, 3625314, 3500621, 3541326, 3553030, 3589274, 3620606, 3622791, 3623801, 3624415, 3624784, 3625370, 3500772, 3541365, 3554960, 3590805, 3620620, 3622849, 3623843, 3624446, 3624805, 3625422, 3502812, 3541546, 3557201, 3597269, 3620626, 3622888, 3623873, 3624449, 3624818, 3625437, 3522442, 3541581, 3560533, 3598374, 3620699, 3622889, 3623877, 3624473, 3624824, 3625443, 3525471, 3541732, 3560780, 3599028, 3620766, 3623048, 3623878, 3624493, 3624825, 3625512, 3526276, 3541857, 3562368, 3600400, 3620769, 3623157, 3623886, 3624497, 3624826, 3625548, 3526801, 3541923, 3563542, 3601482, 3620775, 3623241, 3623895, 3624498, 3624827, 3625634, 3526869, 3541932, 3564532, 3601498, 3620790, 3623244, 3623921, 3624539, 3624828, 3625648, 3527443, 3541971, 3566208, 3601772, 3620887, 3623295, 3623962, 3624541, 3624830, 3625684, 3527832, 3542101, 3566535, 3602192, 3620905, 3623349, 3623985, 3624553, 3624835, 3625685, 3528039, 3542226, 3566790, 3602246, 3621090, 3623416, 3623991, 3624567, 3624838, 3625694, 3528084, 3542278, 3566871, 3607943, 3621234, 3623420, 3624034, 3624572, 3624839, 3625695, 3528271, 3542683, 3569103, 3608133, 3621315, 3623434, 3624069, 3624573, 3624853, 3625698, 3528426, 3542739, 3571487, 3609850, 3621351, 3623441, 3624155, 3624590, 3624905, 3625801, 3528462, 3543043, 3572131, 3609928, 3621354, 3623444, 3624162, 3624591, 3624924, 3625804, 3528535, 3543442, 3572541, 3610434, 3621459, 3623447, 3624173, 3624597, 3624925, 3625805, 3528601, 3543477, 3572696, 3610714, 3621534, 3623452, 3624185, 3624622, 3624930, 3625831, 3530776, 3543509, 3572824, 3611054, 3621591, 3623455, 3624214, 3624623, 3624934, 3625836, 3530964, 3543792, 3572909, 3611702, 3621611, 3623460, 3624221, 3624624, 3624937, 3625913, 3531978, 3543909, 3573095, 3612451, 3621684, 3623493, 3624230, 3624629, 3624966, 3625915, 3532405, 3544169, 3573194, 3614169, 3621705, 3623524, 3624243, 3624639, 3624968, 3625918, 3533275, 3544200, 3573272, 3614468, 3621786, 3623576, 3624252, 3624658, 3624971, 3625921, 3536232, 3544466, 3573666, 3616985, 3621848, 3623584, 3624259, 3624660, 3624982, 3625981, 3537657, 3544530, 3573892, 3617094, 3622007, 3623595, 3624280, 3624661, 3625003, 3626030, 3538453, 3544540, 3573916, 3617407, 3622011, 3623616, 3624283, 3624670, 3625004, 3626032, 3538557, 3544657, 3574481, 3617538, 3622077, 3623636, 3624288, 3624678, 3625025, 3626116, 3538693, 3544745, 3575642, 3617745, 3622086, 3623647, 3624290, 3624700, 3625044, 3626198, 3538779, 3544805, 3575858, 3617883, 3622133, 3623649, 3624297, 3624701, 3625115, 3626232, 3538840, 3544914, 3577824, 3618471, 3622146, 3623653, 3624303, 3624719, 3625132, 3626252, 3538847, 3545023, 3577991, 3618800, 3622148, 3623657, 3624306, 3624721, 3625156, 3626257, 3538867, 3545037, 3578563, 3618934, 3622159, 3623659, 3624339, 3624724, 3625158, 3626515, 3539013, 3545101, 3578574, 3618954, 3622201, 3623665, 3624349, 3624727, 3625186, 3628102, 3539331, 3545730, 3578811, 3619059, 3622364, 3623668, 3624358, 3624729, 3625188, 3629743, 3539375, 3545967, 3579301, 3619592, 3622429, 3623669, 3624379, 3624735, 3625234, 3539423, 3546068, 3585654, 3619625, 3622450, 3623691, 3624380, 3624736, 3625240.
Where was it sold?
Worldwide distribution - US Nationwide distribution in the states of AL, AR, CA, CT, FL, IA, IN, LA, MA, MD, ME, MN, MO, MS, MT, NC, NJ, NY, OH, PA, RI, SC, TN, TX and the country of Puerto Rico.
What should I do if I have it?
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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