RecallRadar

FDA Device recall Z-1508-2014

ToxCup Drug Screen Cup, Catalogue Numbers: HT15, HT15A, PT11, PT11A, PT15A, PT23A, a screening device for the detection of drugs and drug m…

On 2014-04-30 the FDA classified a Class II recall of ToxCup Drug Screen Cup, Catalogue Numbers: HT15, HT15A, PT11, PT11A, PT15A, PT23A, a screening device for the detection of drugs and drug m… by Branan Medical, citing may be labeled with incorrect result interpretation graphics on the ToxCup lid label.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-1508-2014
ClassificationClass II
Statusterminated
Initiated2014-03-26
Published2014-04-30
Last updated2026-09-13 11:53 UTC
CompanyBranan Medical
DistributionUS

Product

ToxCup Drug Screen Cup, Catalogue Numbers: HT15, HT15A, PT11, PT11A, PT15A, PT23A, a screening device for the detection of drugs and drug metabolites in human urine. For in vitro diagnostic use only.

Reason

May be labeled with incorrect result interpretation graphics on the ToxCup lid label.

Identifiers

code_infoLot Numbers: O0056 O0067 N0854 O0013 O0099 O0100 O0057 O0059 O0060 O0079

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1508-2014%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.