Camber Pharmaceuticals Inc: 5 recalls on record

Recalls filed with 1 agency: FDA (5).

First recall on record: March 27, 2019. Most recent: May 17, 2023.

Risk classification: Class I: 1 · Class II: 3 · Class III: 1

Most recent recalls

DateAgencyProduct
May 17, 2023FDAAtovaquone Oral Suspension USP, 750 mg/5 mL, Packaged in 210 mL bottle, Manufactured for:…D-0567-2023
December 21, 2022FDALacosamide Oral Solution, USP, CV, 10mg/mL, packaged in 200 mL bottle, Rx Only, Manufactu…D-0094-2023
March 27, 2019FDALosartan Potassium Tablets USP, 25 mg, Rx only, a) 90 count (NDC 31722-700-90), b) 500 co…D-1041-2019
March 27, 2019FDALosartan Potassium Tablets USP, 50 mg, Rx only, a) 30 count (NDC 31722-701-30), b) 90 cou…D-1042-2019
March 27, 2019FDALosartan Potassium Tablets USP, 100 mg, Rx only, a) 30 count (NDC 31722-702-30), b) 90 co…D-1043-2019

Questions about this company

How many recalls does Camber Pharmaceuticals Inc have?
Recalert has 5 U.S. recalls on record for Camber Pharmaceuticals Inc, published between March 27, 2019 and May 17, 2023.
What was the most recent Camber Pharmaceuticals Inc recall?
FDA recall D-0567-2023, published May 17, 2023: Atovaquone Oral Suspension USP, 750 mg/5 mL, Packaged in 210 mL bottle, Manufactured for: Camber Pharmaceuticals, Inc., Piscataway, NJ 08854, Manufactured by: Hetero Labs Limited, Jeedimetla, Hyderab…
Which agencies have handled Camber Pharmaceuticals Inc recalls?
Camber Pharmaceuticals Inc appears as the recalling firm in recalls from: FDA (5).

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