Recall archive / FDA device enforcement
Sterile Procedural Trays, labeled as the following: a. CELEBRATION ROBOTIC CDS b. DAVINCI CDS UCC-LF c. ROBOTICS PACK... — FDA record Z-1094-2023
Reported ongoing
Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.
Source date Nov 17, 2022. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.
Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.
What the record says
- Product
- Sterile Procedural Trays, labeled as the following: a. CELEBRATION ROBOTIC CDS b. DAVINCI CDS UCC-LF c. ROBOTICS PACK-LF d. ROBOTICS PACK-LF e. ROBOTIC PACK f. PELVISCOPY PACK-LF g. CUSTOM LITHOTOMY ROBOT PACK h. PERI GYN PACK i. ROBOTICS PACK j. LAP HYSTO PACK k. PK, ROBOTICS-ACCESSORY l. OBS PACK m. LAPAROSCOPY/D&C PACK n. PERI GYN RECTAL PACK o. TVT p. DAVINCI DT-LF q. ROBOTICS SI
- Reason
- Sterile blades within sterile kits have the potential for the blade to puncture the outer foil layer of the sterile packaging.
- Classification
- Class II
- Recalling firm
- MEDLINE INDUSTRIES, LP - Northfield
- Quantity
- 1,212 cases (2,101 units)
- Agency-reported status
- Ongoing
- Source record identifier
- Z-1094-2023
What the recall classes mean. Classification is an agency assessment, not individual medical advice.
Lot and product identifiers
| Label field | Details supplied by the agency |
|---|---|
| Lot, code or applicability | a. CELEBRATION ROBOTIC CDS, Item Number: CDS983612C, Case UDI/GTIN: 40884389768687, Unit UDI/GTIN: 10884389768686, Lot Number: 22KBE707,22JBX839,22JBX843; b. DAVINCI CDS UCC-LF, Item Number: CDS984663G, Case UDI/GTIN: 40193489323772, Unit UDI/GTIN: 10193489323771, Lot Number: 22JBX614; c. ROBOTICS PACK-LF, Item Number: DYNJ0038258B, Case UDI/GTIN: 40889942902089, Unit UDI/GTIN: 10889942902088, Lot Number: 22IBO524,22HBV626,22HBV627; d. ROBOTICS PACK-LF, Item Number: DYNJ0046667A, Case UDI/GTIN: 40889942160397, Unit UDI/GTIN: 10889942160396, Lot Number: 22JMA806,22IMC899; e. ROBOTIC PACK, Item Number: DYNJ04135B, Case UDI/GTIN: 40888277893536, Unit UDI/GTIN: 10888277893535, Lot Number: 22JBX625,22IBE470; f. PELVISCOPY PACK-LF, Item Number: DYNJ0843760G, Case UDI/GTIN: 40193489899161, Unit UDI/GTIN: 10193489899160, Lot Number: 22IDC034; g. CUSTOM LITHOTOMY ROBOT PACK, Item Number: DYNJ35094C, Case UDI/GTIN: 40889942764991, Unit UDI/GTIN: 10889942764990, Lot Number: 22IBR203; h. PERI GYN PACK, Item Number: DYNJ39021B, Case UDI/GTIN: 40195327191048, Unit UDI/GTIN: 10195327191047, Lot Number: 22JBI763,22IBJ622; i. ROBOTICS PACK, Item Number: DYNJ42016B, Case UDI/GTIN: 40888277938312, Unit UDI/GTIN: 10888277938311, Lot Number: 22JBQ809,22IBG293; j. LAP HYSTO PACK, Item Number: DYNJ43888, Case UDI/GTIN: 40888277073273, Unit UDI/GTIN: 10888277073272, Lot Number: 22JBC458; k. PK, ROBOTICS-ACCESSORY, Item Number: DYNJ52985F, Case UDI/GTIN: 40193489215824, Unit UDI/GTIN: 10193489215823, Lot Number: 22IBK173,22IBK797,22HBG975; l. OBS PACK, Item Number: DYNJ65258B, Case UDI/GTIN: 40193489829496, Unit UDI/GTIN: 10193489829495, Lot Number: 22IBD122; m. LAPAROSCOPY/D&C PACK, Item Number: DYNJ67569A, Case UDI/GTIN: 40195327191529, Unit UDI/GTIN: 10195327191528, Lot Number: 22JBQ481; n. PERI GYN RECTAL PACK, Item Number: DYNJ82556, Case UDI/GTIN: 40195327198269, Unit UDI/GTIN: 10195327198268, Lot Number: 22IBO110; o. TVT, Item Number: DYNJ900506B, Case UDI/GTIN: 40889942576518, Unit UDI/GTIN: 10889942576517, Lot Number: 22IBV025; p. DAVINCI DT-LF, Item Number: DYNJ900569G, Case UDI/GTIN: 40193489861434, Unit UDI/GTIN: 10193489861433, Lot Number: 22JBB568; q. ROBOTICS SI, Item Number: DYNJ902659D, Case UDI/GTIN: 40889942692416, Unit UDI/GTIN: 10889942692415, Lot Number: 22IBG173,22IBG174 |
Match all identifying details in the current notice. A brand name alone is not enough.
Distribution
Worldwide distribution - US Nationwide and the countries of Canada, Japan, Mexico, Panama, Turks & Caicos, United Arab Emirates.
States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.
- Alaska
- Alabama
- Arkansas
- Arizona
- California
- Colorado
- Connecticut
- Delaware
- Florida
- Georgia
- Hawaii
- Iowa
- Idaho
- Illinois
- Indiana
- Kansas
- Kentucky
- Louisiana
- Massachusetts
- Maryland
- Maine
- Michigan
- Minnesota
- Missouri
- Mississippi
- Montana
- North Carolina
- North Dakota
- Nebraska
- New Hampshire
- New Jersey
- New Mexico
- Nevada
- New York
- Ohio
- Oklahoma
- Oregon
- Pennsylvania
- Rhode Island
- South Carolina
- South Dakota
- Tennessee
- Texas
- Utah
- Virginia
- Vermont
- Washington
- Wisconsin
- West Virginia
- Wyoming
Dates in the source
- Report date
- Feb 15, 2023
- Recall initiation date
- Nov 17, 2022
- Center classification date
- Feb 6, 2023
FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.