AVID Medical Robotic Prostatectomy Pack May Be Contaminated with Lubricant
AVID Medical recalls 6 units of Robotic Prostatectomy Pack (Model NAMC423-11) due to potential lubricant contamination during manufacturing. Affected units were distributed nationwide in AZ, CA, FL, MD, NE, TX.
Recall notice
Product may be potentially contaminated with a lubricant used during the manufacturing process.
What happened, in plain English
AVID Medical is recalling 6 robotic prostatectomy packs that may contain lubricant from the manufacturing process. This could pose a risk of contamination during surgical procedures. Read more at govinfonow.com/recall/1629653-avid-medical-inc-recalls-robotic-prostatectomy-pack-model-item-number.
Source Summary by GovInfoNow · govinfonow.com/recall/1629653-avid-medical-inc-recalls-robotic-prostatectomy-pack-model-item-number · Updated October 21, 2026 · FDA enforcement record: FDA #Z-0098-2027
Cite this page
“AVID Medical Robotic Prostatectomy Pack May Be Contaminated with Lubricant.” GovInfoNow, updated October 21, 2026. https://govinfonow.com/recall/1629653-avid-medical-inc-recalls-robotic-prostatectomy-pack-model-item-number. Based on FDA recall #Z-0098-2027 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0098-2027%22&limit=1).
Why it’s dangerous
The product may have been contaminated with a lubricant used during manufacturing. This could lead to unintended exposure during surgical procedures if the lubricant is not properly cleaned or handled.
Who’s affected
Surgical teams using the recalled robotic prostatectomy packs in the U.S. states of AZ, CA, FL, MD, NE, and TX are most at risk. The specific number of affected units is limited to 6.
How to tell if you have this one
Check for the model number NAMC423-11 on the pack. The kit lot numbers include 1671502 and the supplier lot number NGKT2404. These units were distributed nationwide in AZ, CA, FL, MD, NE, and TX.
- Brand
AVID Medical- Category
Medical device
All 15 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
US Nationwide distribution in the states of AZ, CA, FL, MD, NE, TX.
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| Z-0092-2027 | DAVINCI TRUCUSTOM BUNDLE; Model/Item Number (Kit): 1. SAMM064-27, 2. SAMM064-28;; 1. Model/Item Number (Kit): SAMM064-27; UDI-DI: 10809160439708; Kit Lot Numbers: 1657586, 1658104, 1671251; 2. Model/Item Number (Kit): SAMM064-28; UDI-DI: 10809160516201; Kit Lot Numbers: 1698700; Recalled Supplier Component (in kit): A303416A; Recalled Supplier Lot Number (in kit): NGKU1749, NGKV0359; | 144 |
| Z-0093-2027 | GYN LAPAROSCOPY/LAPAROTOMY; Model/Item Number (Kit): 1. WRNM002-15, 2. FBCH108-03;; 1. Model/Item Number (Kit): WRNM002-15; UDI-DI: 10809160487181; Kit Lot Numbers: 1666722; 2. Model/Item Number (Kit): FBCH108-03; UDI-DI: 10809160399781; Kit Lot Numbers: 1659079, 1696378; Recalled Supplier Component (in kit): A942216; Recalled Supplier Lot Number (in kit): NGKU3975, NGKU2887; | 134 |
| Z-0094-2027 | ADULT HEART TRAY SHANDS JACKS; Model/Item Number (Kit): SHND419-08;; 1. Model/Item Number (Kit): SHND419-08; UDI-DI: 10809160502389; Kit Lot Numbers: 1680504, 1695337; Recalled Supplier Component (in kit): A319514AM; Recalled Supplier Lot Number (in kit): NGKW2687, NGKV2393; | 59 |
| Z-0095-2027 | ENDOVASCULAR PACK; Model/Item Number (Kit): VAPX014-04;; 1. Model/Item Number (Kit): VAPX014-04; UDI-DI: 10809160332863; Kit Lot Numbers: 1701106, 1702175, 1702273; Recalled Supplier Component (in kit): A902416; Recalled Supplier Lot Number (in kit): NGKU4043; | 33 |
| Z-0096-2027 | CRANIOTOMY PACK; Model/Item Number (Kit): WRNM035-20;; 1. Model/Item Number (Kit): WRNM035-20; UDI-DI: 10809160489277; Kit Lot Numbers: 1695943; Recalled Supplier Component (in kit): A319516AM; Recalled Supplier Lot Number (in kit): NGKT2391; | 10 |
| Z-0097-2027 | PACK OPEN HEART CFH; Model/Item Number (Kit): 1. UFCF004-06, 2. UFCF004-07;; 1. Model/Item Number (Kit): UFCF004-06; UDI-DI: 10809160487334; Kit Lot Numbers: 1666214, 1672814; 2. Model/Item Number (Kit): UFCF004-07; UDI-DI: 10809160513170; Kit Lot Numbers: 1695181; Recalled Supplier Component (in kit): A119216M; Recalled Supplier Lot Number (in kit): NGKT2404, NGKT3314; | 124 |
| Z-0098-2027 | ROBOTIC PROSTATECTOMY PACK; Model/Item Number (Kit): NAMC423-11;; Model/Item Number (Kit): NAMC423-11; UDI-DI: 10809160490808; Kit Lot Numbers: 1671502; Recalled Supplier Component (in kit): A119216M; Recalled Supplier Lot Number (in kit): NGKT2404; | 6 |
| Z-0099-2027 | LAPAROSCOPIC PROSTATECTOMY; Model/Item Number (Kit): NIHB0036-07;; Model/Item Number (Kit): NIHB0036-07; UDI-DI: 10809160403099; Kit Lot Numbers: 1657751; Recalled Supplier Component (in kit): A942216; Recalled Supplier Lot Number (in kit): NGKT3375; | 15 |
| Z-0100-2027 | PLASTICS TRAY; Model/Item Number (Kit): EURO053;; Model/Item Number (Kit): EURO053; UDI-DI: 10809160423813; Kit Lot Numbers: 1674613; Recalled Supplier Component (in kit): A902416; Recalled Supplier Lot Number (in kit): NGKU3975; | 28 |
| Z-0101-2027 | DAVINCI LAP/GYN; Model/Item Number (Kit): WRNM037-16;; Model/Item Number (Kit): WRNM037-16; UDI-DI: 10809160468913; Kit Lot Numbers: 1663589; Recalled Supplier Component (in kit): A942216; Recalled Supplier Lot Number (in kit): NGKT3375; | 30 |
| Z-0102-2027 | HEART PREP TRAY; Model/Item Number (Kit): MECV97W;; Model/Item Number (Kit): MECV97W; UDI-DI: 10809160493113; Kit Lot Numbers: 1691836, 1696316; Recalled Supplier Component (in kit): A319514AM; Recalled Supplier Lot Number (in kit): NGKV2393; | 96 |
| Z-0103-2027 | UROLOGY MAJOR; Model/Item Number (Kit): WRNM058-10;; Model/Item Number (Kit): WRNM058-10; UDI-DI: 10809160488898; Kit Lot Numbers: 1681989; Recalled Supplier Component (in kit): A902416; Recalled Supplier Lot Number (in kit): NGKU2887; | 20 |
| Z-0104-2027 | MAJOR PACK; Model/Item Number (Kit): NIHB0018-11;; Model/Item Number (Kit): NIHB0018-11; UDI-DI: 10809160403747; Kit Lot Numbers: 1667763; Recalled Supplier Component (in kit): A942216; Recalled Supplier Lot Number (in kit): NGKT3375; | 40 |
| Z-0105-2027 | GYN LAPAROSCOPY PACK; Model/Item Number (Kit): NAMC436-12;; Model/Item Number (Kit): NAMC436-12; UDI-DI: 10809160468470; Kit Lot Numbers: 1697826; Recalled Supplier Component (in kit): A119216M; Recalled Supplier Lot Number (in kit): NGKT3314; | 28 |
| Z-0106-2027 | ABD HYSTERECTOMY; Model/Item Number (Kit): NAMC438-07;; Model/Item Number (Kit): NAMC438-07; UDI-DI: 10809160417645; Kit Lot Numbers: 1675123, 1675125, 1679551; Recalled Supplier Component (in kit): A119216M; Recalled Supplier Lot Number (in kit): NGKT2404; | 23 |
What to do — step by step
Check Product Details
Identify the model number NAMC423-11 and lot numbers 1671502 or NGKT2404 on the pack.
Where it went and when
Where it was distributed
Distributed nationwide; the notice names 6 states.
FDA distribution: “US Nationwide distribution in the states of AZ, CA, FL, MD, NE, TX.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: Arizona, California, Florida, Maryland, Nebraska, Texas.
Recall timeline
FDA published this recall 2 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- Added to GovInfoNow
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-0098-2027 (August 10, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0098-2027 to see it in context.
- Plain-language summary written by qwen3:4b on October 21, 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.