FDA Device recall Z-2873-2016
LifeCare PCA Infusion System with Hospira MedNet Software, PCA Serial List Number 20709 Allows for clinician administration or self-adminis…
- FDA Device
- Class II
- terminated
- Published 2016-09-28
On 2016-09-28 the FDA classified a Class II recall of LifeCare PCA Infusion System with Hospira MedNet Software, PCA Serial List Number 20709 Allows for clinician administration or self-adminis… by Hospira, citing screw rotation error occurring when the pump detects a mismatch between the number of steps given to the motor driving delivery and the number of steps the motor actually took. Wh….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2873-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-03-08 |
| Published | 2016-09-28 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Hospira |
| Distribution | US |
Product
LifeCare PCA Infusion System with Hospira MedNet Software, PCA Serial List Number 20709 Allows for clinician administration or self-administration of analgesic medications.
Reason
Screw rotation error occurring when the pump detects a mismatch between the number of steps given to the motor driving delivery and the number of steps the motor actually took. When this malfunction occurs, the pump will alarm and infusion stops.
Identifiers
| code_info | Serial Number 15553367, 16224548, 16224939, 16225091, 16225646, 16225851, 16226006, 16226095, 16226117…Serial Number 15553367, 16224548, 16224939, 16225091, 16225646, 16225851, 16226006, 16226095, 16226117, 16226159, 16226360, 16226383, 16226435, 16226460, 16226680, 16226707, 16226726, 16226730, 16226756, 16226763, 16226891, 16226895, 16226898, 16226910, 16226917, 16226918, 16226919, 16226920, 16226921, 16226922, 16226923, 16226924, 16226925, 16226926, 16226927, 16226928, 16226929, 16226930, 16226931, 16226932, 16226933, 16226934, 16226935, 16226936, 16226937, 16226938, 16226939, 16226940, 16226941, 16226943, 16226944, 16226945, 16226946, 16226947, 16226948, 16226949, 16226950, 16226951, 16226952, 16226953, 16226954, 16226955, 16226956, 16226957, 16226958, 16226959, 16226960, 16226961, 16226962, 16226963, 16226964, 16226965, 16226966, 16226967, 16226968, 16226969, 16226970, 16226971, 16226972, 16226973, 16226974, 16226975, 1 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Other recalls by Hospira
- Infant 25% DEXTROSE Injection, USP, 2.5 g (250 mg/mL), 10 mL Unit of Use Single-dose Syringe per carton, Rx only, Hospira Inc., Lake Forest…
FDA Drug · Class I · 2017-05-31 · Hospira - Minibore Extension Set, 59 Inch with Spin Lock Collar, Non-DEHP, Latex-Free Intended use: For the administration of drugs and solutions to…
FDA Device · Class II · 2017-01-18 · Hospira - 5% Lidocaine HCL and 7.5% Dextrose Injection, USP, 2 mL Single-dose ampule, 5 count box, Rx Only, For Spinal Anesthesia Only, Manufactured…
FDA Drug · Class III · 2016-12-14 · Hospira - Fentanyl Citrate Injection, USP, 100 mcg Fentanyl/ 2mL, Single Dose, 50 mcg/mL, Rx only, Hospira, Inc., Lake Forest IL 60045, NDC 0409-4093…
FDA Drug · Class II · 2016-11-30 · Hospira - Symbiq Two Channel Infuser
FDA Device · Class II · 2016-11-16 · Hospira
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2873-2016%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.