FDA Device recall Z-2047-2025

Bravo CF capsule delivery device, designed to place and attach a pH monitoring capsule to the esophagus using endoscopic or manometric guid…

FDA Device
Class I
ongoing
Published 2025-07-16

On 2025-07-16 the FDA classified a Class I recall of Bravo CF capsule delivery device, designed to place and attach a pH monitoring capsule to the esophagus using endoscopic or manometric guid… by Given Imaging, citing it has been determined that misapplied adhesive on the Bravo CF capsule delivery device may lead to its malfunction. Specifically, the misapplied adhesive may prevent the capsule….

Read the official FDA Device notice

Agency	FDA Device
Recall number	Z-2047-2025
Classification	Class I
Status	ongoing
Initiated	2025-06-03
Published	2025-07-16
Last updated	2026-09-13 11:57 UTC
Company	Given Imaging
Distribution	US

Product

Bravo CF capsule delivery device, designed to place and attach a pH monitoring capsule to the esophagus using endoscopic or manometric guidance, Product Number FGS-0635 (5 pack) and FGS-0636 (1 pack)

Reason

It has been determined that misapplied adhesive on the Bravo CF capsule delivery device may lead to its malfunction. Specifically, the misapplied adhesive may prevent the capsule from attaching to the patient's esophagus or detaching from the delivery device.

Identifiers

code_info	FGS-0635: UDI-DI: 07290101369707; Lot Numbers: 61164F 61407F 61933F 62142F 62418F 62884F 63152F 63668F 64065F 64096F 64… FGS-0635: UDI-DI: 07290101369707; Lot Numbers: 61164F 61407F 61933F 62142F 62418F 62884F 63152F 63668F 64065F 64096F 64291F 61165F 61408F 61934F 62143F 62419F 62885F 63154F 63669F 64066F 64261F 64550F 61166F 61409F 61935F 62144F 62420F 62886F 63155F 63670F 64067F 64262F 64551F 61167F 61410F 61936F 62145F 62421F 62887F 63156F 63671F 64068F 64263F 64552F 61168F 61411F 61937F 62146F 62422F 62888F 63157F 63672F 64069F 64264F 64553F 61169F 61412F 61938F 62147F 62656F 62889F 63158F 63673F 64070F 64265F 64554F 61170F 61413F 61939F 62148F 62657F 62890F 63159F 63674F 64071F 64266F 64555F 61171F 61414F 61940F 62149F 62658F 62891F 63391F 63675F 64072F 64267F 64557F 61172F 61415F 62031F 62150F 62659F 62892F 63392F 63676F 64073F 64268F 64558F 61173F 61416F 62032F 62151F 62660F 62893F 63393F 63677F 64074F 64269F 64559F 61352F 61708F 62033F 62152F 62661F 62894F 63394F 63679F 64075F 64270F 64560F 61386F 61709F 62034F 62153F 62662F 62895F 63395F 63680F 64076F 64271F 64561F 61387F 61711F 62035F 62154F 6

code_info

FGS-0635: UDI-DI: 07290101369707; Lot Numbers: 61164F 61407F 61933F 62142F 62418F 62884F 63152F 63668F 64065F 64096F 64…

FGS-0635: UDI-DI: 07290101369707; Lot Numbers: 61164F 61407F 61933F 62142F 62418F 62884F 63152F 63668F 64065F 64096F 64291F 61165F 61408F 61934F 62143F 62419F 62885F 63154F 63669F 64066F 64261F 64550F 61166F 61409F 61935F 62144F 62420F 62886F 63155F 63670F 64067F 64262F 64551F 61167F 61410F 61936F 62145F 62421F 62887F 63156F 63671F 64068F 64263F 64552F 61168F 61411F 61937F 62146F 62422F 62888F 63157F 63672F 64069F 64264F 64553F 61169F 61412F 61938F 62147F 62656F 62889F 63158F 63673F 64070F 64265F 64554F 61170F 61413F 61939F 62148F 62657F 62890F 63159F 63674F 64071F 64266F 64555F 61171F 61414F 61940F 62149F 62658F 62891F 63391F 63675F 64072F 64267F 64557F 61172F 61415F 62031F 62150F 62659F 62892F 63392F 63676F 64073F 64268F 64558F 61173F 61416F 62032F 62151F 62660F 62893F 63393F 63677F 64074F 64269F 64559F 61352F 61708F 62033F 62152F 62661F 62894F 63394F 63679F 64075F 64270F 64560F 61386F 61709F 62034F 62153F 62662F 62895F 63395F 63680F 64076F 64271F 64561F 61387F 61711F 62035F 62154F 6

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2047-2025%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.