Claris Lifesciences recalls
Claris Lifesciences appears in 5 official U.S. recall notices indexed by RecallRadar, most recently on 2017-12-27.
Company names are normalized from agency data (legal suffixes removed), so related firms may appear under separate pages.
Recall summary
| Recall notices | 5 |
|---|---|
| Published | 2017-04-05 to 2017-12-27 |
| By agency | FDA Drug (5) |
| By classification | Class II (4), Class III (1) |
| By status | terminated (5) |
| Distribution named in notices | US |
Recalls
- Ciprofloxacin in Dextrose (5%) Injection, USP 200 mg in 100 mL 5% Dextrose, Rx Only, (2 mg/mL), 100 mL Flexible Bag, Manufactured for: Clar…
FDA Drug · Class III · 2017-12-27 · Claris Lifesciences
Reason: Superpotent - Levofloxacin Injection in 5% Dextrose, 750 mg in 150 mL 5% Dextrose, Rx only, Manufactured for: Claris Lifesciences Inc
FDA Drug · Class II · 2017-04-05 · Claris Lifesciences
Reason: Lack of Assurance of Sterility: there is potential of a leak from the primary container which may result in a potential breach of sterility and contamination of the product. - Ciprofloxacin in Dextrose (5%) Injection, USP, 400 mg in 200 mL 5% Dextrose, Rx only, Manufactured for: Claris Lifesciences Inc
FDA Drug · Class II · 2017-04-05 · Claris Lifesciences
Reason: Lack of Assurance of Sterility: there is potential of a leak from the primary container which may result in a potential breach of sterility and contamination of the product. - Metronidazole Injection, USP, 500 mg/100 mL, Rx only, Manufactured for: Claris Lifesciences Inc
FDA Drug · Class II · 2017-04-05 · Claris Lifesciences
Reason: Lack of Assurance of Sterility: there is potential of a leak from the primary container which may result in a potential breach of sterility and contamination of the product. - Fluconazole Injection, USP, 400 mg in 200 mL, Rx only, Manufactured for: Claris Lifesciences Inc
FDA Drug · Class II · 2017-04-05 · Claris Lifesciences
Reason: Lack of Assurance of Sterility: there is potential of a leak from the primary container which may result in a potential breach of sterility and contamination of the product.