Quelicin recalls
Quelicin products have been recalled 3 times, most recently on 9 Aug 2017. The recalling company is usually Hospira. The most common reason is sterility.
Total recalls3since 2013
Last 12 months0reported
Class I00% of total
Ongoing1latest 9 Aug 2017
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 2 67%Class III 1 33%
Why quelicin is recalled
Companies
Product types
By year
Ongoing quelicin recalls
1 active| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS III | Quelicin (Succinylcholine Chloride) Injection, USP 200 mg recalledQuelicin | Hospira | Foreign Material | Nationwide |
All quelicin recalls, newest first
3 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Succinylcholine Chloride Injection, USP 200 mg recalledQuelicin | Hospira a Pfizer | Sterility | PR |
| Drug | CLASS III | Quelicin (Succinylcholine Chloride) Injection, USP 200 mg recalledQuelicin | Hospira | Foreign Material | Nationwide |
| Drug | CLASS II | Quelicin (succinylcholine chloride) Injection, USP, 200 mg recalledQuelicin | Hospira | Sterility | Nationwide |
About this list
Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.