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Lower risk Medical device recall · FDA · Published June 11, 2025

AVID Medical GYN ROBOTIC PACK Recall: Discoloration from resterilization

AVID Medical recalls GYN ROBOTIC PACK kits due to discoloration from resterilization. Affected kits have specific model and lot numbers. No action is required as the hazard is cosmetic.

🇺🇸 FDA recall #Z-2251-2025Medical deviceAVID Medical ›
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Recalling firmAVID Medical, Inc.9000 Westmont Dr · Toano, VA 23168-9351
✎ GovInfoNow plain-language explainer

What happened, in plain English

AVID Medical is recalling GYN ROBOTIC PACK medical kits because discoloration occurred during resterilization. This issue does not pose a safety risk but may affect appearance. No action is needed as the problem is cosmetic. Read more at govinfonow.com/recall/52055-avid-medical-gyn-robotic-pack-recall-discoloration-from-resterilization.

Source Summary by GovInfoNow · govinfonow.com/recall/52055-avid-medical-gyn-robotic-pack-recall-discoloration-from-resterilization · Updated August 17, 2026 · FDA enforcement record: FDA #Z-2251-2025

Cite this page

“AVID Medical GYN ROBOTIC PACK Recall: Discoloration from resterilization.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/52055-avid-medical-gyn-robotic-pack-recall-discoloration-from-resterilization. Based on FDA recall #Z-2251-2025 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2251-2025%22&limit=1).

Why it’s dangerous

The CLEARIFY VISUALIZATION SYSTEM in the kits was inadvertently resterilized, causing discoloration. This discoloration is a cosmetic issue and does not affect the functionality or safety of the product.

Who’s affected

Medical professionals using the GYN ROBOTIC PACK kits with model NAMC474-01 and specific lot numbers are affected. The risk is minimal as the discoloration is cosmetic and not a safety hazard.

How to tell if you have this one

Check for model number NAMC474-01 and lot numbers 1620573, 1620572, 1621883, 1621884, or 1628673 on the kit packaging or label.

  • Brand
    AVID Medical
  • Category
    Medical device
FDA recall event · 24 products

All 24 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Classification
    Class II
  • Status
    Ongoing
  • Distribution
    Domestic: CA, IL, MD, OH, PA, TX, WA.
Recall numberProduct, codes & lotsQuantity
Z-2240-2025LAPAROSCOPIC TRAY. Medical convenience kit.; Model No. BJAC006-27; UDI: 10809160394540; Kit Lot No. 1599252, 1609971, 1612404, 1640192.40 units
Z-2241-2025CARDIAC ROBOT PACK. Medical convenience kit.; Model No. RYCB72-03; UDI: 10809160422830; Kit Lot No. 1608339.20 units
Z-2242-2025CT DAVINCI. Medical convenience kit.; Model No. WRNM089; UDI: 10809160432525; Kit Lot No. 1627141.12 units
Z-2243-2025DA VINCI PACK URO/PROSTATE. Medical convenience kit.; Model No. VAHT009-19; UDI: 10809160378748; Kit Lot No. 1579555.21 units
Z-2244-2025DAVINCI TRUCUSTOM BUNDLE. Medical convenience kit.; Model No. MAMC228-13, MAMC228-14, MAMC228-15; UDI: 10809160366943, 10809160366820, 10809160420980, 10809160421734, 10809160441046; Kit Lot No. 1576797, 1577255, 1586536, 1606044, 1607044, 1607825, 1615452, 1621487, 1621488, 1638247, 1639254, 1647833.626 units
Z-2245-2025DAVINCI UROLOGY. Medical convenience kit.; Model No. WRNM038-09, WRNM038-10, WRNM038-11; UDI: 10809160369302, 10809160418338, 10809160432259; Kit Lot No. 1589886, 1593087, 1606686, 1606688, 1615262, 1611133, 1627007.166 units
Z-2246-2025GEN LAPAROSCOPY PACK. Medical convenience kit.; Model No. VMCC007-12; UDI: 10809160357200; Kit Lot No. 1592617, 1598707, 1608042, 1608043, 1621654.321 units
Z-2247-2025GENERAL LAPAROSCOPY TRAY. Medical convenience kit.; Model No. EURO010-08, USAR042-17, WILF006-29; UDI: 10809160414309, 10809160400586, 10809160429914, 10809160431108; Kit Lot No. 1616570, 1581675, 1594938, 1597550, 1600846, 1620149, 1620150, 1620151, 1622920.574 units
Z-2248-2025GENERAL ROBOTIC PACK. Medical convenience kit.; Model No. NAFB082-04, NAMC473-01; UDI: 10809160395691, 10809160375037; Kit Lot No. 1568211, 1576237, 1599515, 1599516, 1605944, 1613558, 1616420, 1613626, 1625831, 1627259, 1628672, 1632042, 1635911.203 units
Z-2249-2025GS ENDOSCOPY PACK. Medical convenience kit.; Model No. NAMC421-10, NAMC421-11, NAMC421-12; UDI: 10809160374597, 10809160417539, 10809160435779; Kit Lot No. 1584375, 1588403, 1605341, 1615427, 1615428, 1627706, 1628153, 1628008, 1628009, 1628647, 1632992.816 units
Z-2250-2025GYN LAPAROSCOPY PACK. Medical convenience kit.; Model No. NAFB055-08, NAMC436-11, VMCC030-06; UDI: 10809160405185, 10809160417621, 10809160415245, 10809160419021; Kit Lot No. 1595523, 1598524, 1598523, 1628236, 1634348, 1636865, 1645025, 1645227, 1608234, 1608349, 1608466, 1613607, 1613139, 1613608, 1616927, 1622475, 1628656, 1632993, 1596145, 1603597, 1608059, 1619856.346 units
Z-2251-2025GYN ROBOTIC PACK. Medical convenience kit.; Model No. NAMC474-01; UDI: 10809160375044; Kit Lot No. 1620573, 1620572, 1621883, 1621884, 1628673.45 units
Z-2252-2025HVI CARDIAC ROBOT PACK. Medical convenience kit.; Model No. RYCB72-04; UDI: 10809160434666; Kit Lot No. 1625487.20 units
Z-2253-2025LAP CHOLE PACK. Medical convenience kit.; Model No. VCIH007-06; UDI: 10809160379479, 10809160450758; Kit Lot No. 1569227, 1569228, 1569229, 1589126, 1608615, 1623944, 1643426.85 units
Z-2254-2025LAPAROSCOPIC GYN. Medical convenience kit.; Model No. EURO011-08; UDI: 10809160414248; Kit Lot No. 1613056.18 units
Z-2255-2025LAPAROSCOPIC PROSTATECTOMY. Medical convenience kit.; Model No. NIHB0036-07; UDI: 10809160403099; Kit Lot No. 1589877, 1612565.30 units
Z-2256-2025LAPAROSCOPY PACK. Medical convenience kit.; Model No. VAML025-05, WRNM007-15; UDI: 10809160387696, 10809160432235; Kit Lot No. 1580078, 1580079, 1580407, 1582536, 1585729, 1596605, 1598248, 1598249, 1607780, 1626103, 1629350, 1639643, 1627004.452 units
Z-2257-2025LAVH PACK. Medical convenience kit.; Model No. USAR053-11; UDI: 10809160372357; Kit Lot No. 1578109, 1585712, 1597106, 1601742, 1601643, 1607925, 1612044, 1621429, 1637117.292 units
Z-2258-2025MAJOR THORACOSCOPY BASIN. Medical convenience kit.; Model No. NIHB0022-09, NIHB0022-11, NIHB0022-12; UDI: 10809160381311, 10809160403730, 10809160440940; Kit Lot No. 1580032, 1590461, 1590463, 1604743, 1613180, 1613182, 1618989, 1641040.128 units
Z-2259-2025PACK GENERAL ROBOTIC. Medical convenience kit.; Model No. RDLD047-10; UDI: 10809160358603; Kit Lot No. 1589630, 1590570, 1610157, 1617028, 1618142, 1621537, 1629589, 1635288, 1636852.656 units
Z-2260-2025PARTIAL NEPHRECTOMY - ROBOTIC. Medical convenience kit.; Model No. NIHB0035-07; UDI: 10809160404959; Kit Lot No. 1591938, 1622268, 1628944, 1632685.46 units
Z-2261-2025PARTIAL NEPHRECTOMY PACK. Medical convenience kit.; Model No. NAMC077, NAMC077-02; UDI: 10809160318911, 10809160437971; Kit Lot No. 1591073, 1612261, 1616916, 1632036, 1632038, 1632359.52 units
Z-2262-2025ROBOTIC PROSTATECTOMY PACK. Medical convenience kit.; Model No. NAMC423-08; UDI: 10809160374627; Kit Lot No. 1624611, 1624612, 1628010.24 units
Z-2263-2025ROBOTIC URO/GYN PACK. Medical convenience kit.; Model No. RDLD050-09; UDI: 10809160413715; Kit Lot No. 1604510, 1604511, 1604512, 1606486, 1629590, 1633995, 1633997.372 units
Based on the official FDA remedy

What to do — step by step

  1. Check for Discoloration

    Inspect the kit for discoloration, which is a cosmetic issue not affecting safety.

Where it went and when

Where it was distributed

Distributed in 7 states.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: yesWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: yesILWisconsin: not listedWIMichigan: not listedMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: yesOHPennsylvania: yesPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: yesCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: yesMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: yesTXFlorida: not listedFL

FDA distribution: “Domestic: CA, IL, MD, OH, PA, TX, WA.” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: California, Illinois, Maryland, Ohio, Pennsylvania, Texas, Washington.

Recall timeline

FDA published this recall 2 months after the firm started it.

1. Firm started the recall: Jun 11, 202512. FDA classified it Class II: Aug 4, 202523. Published in FDA’s Enforcement Report: Aug 13, 202532025
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #Z-2251-2025 (June 11, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2251-2025 to see it in context.
  • Plain-language summary written by qwen3:4b on August 17, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA