RecallRadar

FDA Drug recall D-1083-2017

Phentermine HCL Capsules, USP 15 mg, packaged in a) 100-count bottles (NDC 10702-026-01), and b) 1000-count bottles (NDC 10702-026-10), Rx…

On 2017-08-23 the FDA classified a Class III recall of Phentermine HCL Capsules, USP 15 mg, packaged in a) 100-count bottles (NDC 10702-026-01), and b) 1000-count bottles (NDC 10702-026-10), Rx… by Kvk Tech, citing failed Impurities/Degradation Specifications: out-of-specification results obtained for individual unknown impurities found at 30 month Room Temperature Retained Sample stability….

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-1083-2017
ClassificationClass III
Statusterminated
Initiated2017-08-03
Published2017-08-23
Last updated2026-09-13 11:51 UTC
CompanyKvk Tech
DistributionUS

Product

Phentermine HCL Capsules, USP 15 mg, packaged in a) 100-count bottles (NDC 10702-026-01), and b) 1000-count bottles (NDC 10702-026-10), Rx only, mfd. by: KVK-TECH, INC. NEWTOWN, PA 18940

Reason

Failed Impurities/Degradation Specifications: out-of-specification results obtained for individual unknown impurities found at 30 month Room Temperature Retained Sample stability test.

Identifiers

ndc10702-026-03
ndc10702-026-01
ndc10702-026-10
ndc10702-027-03
ndc10702-027-01
ndc10702-027-10
ndc10702-028-03
ndc10702-028-01
ndc10702-028-10
code_infoLot # a):12322A, 12323B, 12324A, Exp. Sep 2017; 12455A, Exp. Dec 2017; b) 12323A, Exp. Sep 2017; 12456A, Exp. Dec 2017

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1083-2017%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.