Hospira Buprenorphine Hydrochloride Injection and Labetalol Hydrochloride Injection - recalled due to Packaging Defect, USA
3 weeks ago •source fda.gov • details
Recall notice
2 years ago • business
Regulatory Report
12851 Prospect Street, Dearborn, 48126 Michigan, United States
1. An employee tested Covid-19 positive. 2. Employees with close contact were not provided paperwork by the employer to get tested at the work clinic or told where to go. 3. Employees are required to share their results and have to return to work before their 14-day quarantine period is up. 4. Mask use is not enforced.3 weeks ago •source fda.gov • details
Recall notice
1 week ago •reported by user-zkkc1731 • details
6 days ago •reported by user-zrnp2455 • details
1 week ago •reported by user-gyydb912 • details
4 weeks ago •reported by user-tgcg2937 • details
1 week ago •reported by user-zxpv5363 • details
3 weeks ago •reported by user-hqyzn279 • details
2 weeks ago •reported by user-vjydv832 • details
2 weeks ago •reported by user-knzzj639 • details
2 weeks ago •reported by user-hwzcy465 • details
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