Product Safety Recalls

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Lucid Diagnostics, Inc. Recall 94510

Description: Brand Name: EsophaCap Product Name: EsophaCap (25mm diameter, 10 pores/inch) Model/Catalog Number: EC25T10VI Software Version: N/A Product Description: EsophaCap is pouched as individual units. 10 units go into a shelf-box. Component: N/A

Lucid Diagnostics, Inc. Recall 94510 Information

StatusOngoing
Mandated?Voluntary: Firm initiated
Recall NumberZ-1900-2024
Event ID94510
Event DescriptionBrand Name: EsophaCap Product Name: EsophaCap (25mm diameter, 10 pores/inch) Model/Catalog Number: EC25T10VI Software Version: N/A Product Description: EsophaCap is pouched as individual units. 10 units go into a shelf-box. Component: N/A
Product TypeDevices
DistributionUS Nationwide distribution in the states of MN, MD.
Quantity220 units (US)
Recall ReasonThe EsophaCap sponge may be at increased risk of detaching from the string during removal of the device from the patient, particularly at the lower esophageal sphincter at the gastroesophageal junction or the upper esophageal sphincter between the pharynx and the esophagus, which is the narrowest part of the alimentary canal.
Device Classification20240605
Device Code InfoLot Code: Product sent out to clinical site: Part #: EC25T10VI ; GTIN Number: 00860007510977 ; Lot #'s: 483 (Qty: 120), 502 (Qty: 100) Product at Distributor in Quarantine: Part #: EC25T10VI ; GTIN Number: 00860007510977 ; Lot #'s: 539 (Qty: 99)
Center Classification Date20240524
Recall Initiation Date20240424
Recalling FirmLucid Diagnostics, Inc.
Initial Notification Letter
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