Lower riskMedical device recall · FDA · Published March 6, 2020
Cook Spectrum Central Venous Catheter Tray: Incorrect Expiration Dates
Cook recalls Spectrum Central Venous Catheter Tray with incorrect printed expiration dates. This may lead to improper use of medical devices. Affected units include specific part numbers and lot numbers.
“Cook Spectrum Central Venous Catheter Tray: Incorrect Expiration Dates.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/65705-cook-spectrum-central-venous-catheter-tray-incorrect-expiration-dates. Based on FDA recall #Z-1566-2020 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1566-2020%22&limit=1).
Cook Inc. recalled the Spectrum Central Venous Catheter Tray due to incorrect printed expiration dates, according to the FDA on March 6, 2020.
How to tell if you have it
Brand: Cook
Product: Spectrum Central Venous Catheter Tray, Irrigation Catheter
Reference Part Number: C-UDLMY-401 J-ABRM-HC-IHl-FST
Order Number: G48053
Lot Number: 10235662
UDI: (01)00827002480537(17)562310(10)10235662
UPC: 00827002480537
The hazard
The printed expiration dates on the Spectrum Central Venous Catheter Tray are incorrect, according to the FDA.
Context
GovInfoNow's records show Cook Inc. has 38 other recalls on record since July 31, 2017. Recent Cook recalls include a Nov. 12, 2021, check-flo introducer mislabeling risk and an Oct. 13, 2021, needle debris recall for inflammatory reactions. Other recent recalls of similar products include Cook Spectrum Central Venous Catheter Tray expiration date errors on March 5, 2026, and Cook Medical Spectrum Central Venous Catheter Sets expiration date issues on the same date.
How to tell if you have this one
Check for the reference part number C-UDLMY-401 J-ABRM-HC-IHl-FST, order number G48053, lot number 10235662, or UDI (01)00827002480537(17)562310(10)10235662 on the product.
Brand
Cook
Product
Spectrum Central Venous Catheter Tray, Irrigation Catheter, Reference Part Number C-UDLMY-401 J-ABRM-HC-IHl-FST, Order
Category
Medical device
FDA recall event · 2 products
All 2 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
Terminated
Distribution
The products were distributed to the following US states: CO, DE, MD, MN, NC, NV, and WV. The products were distributed to the following foreign countries: Canada.
Recall number
Product, codes & lots
Z-1565-2020
Pericardiocentesis Set, Irrigation Catheter, Reference Part Number C-PCS-700-TORONT0-042997, Order Number G10643; Lot Number 10119247; UDI: (01)00827002106437(17)921110(10)10119247
Z-1566-2020
Spectrum Central Venous Catheter Tray, Irrigation Catheter, Reference Part Number C-UDLMY-401 J-ABRM-HC-IHl-FST, Order Number G48053; Lot Number 10235662; UDI: (01)00827002480537(17)562310(10)10235662
Based on the official FDA remedy
What to do — step by step
Check Expiration Date
Verify the printed expiration date on the catheter tray and irrigation catheter against the correct date.
Where it went and when
Where it was distributed
Distributed in 7 states, and outside the U.S.
Listed by the agency
Not listed
FDA distribution: “The products were distributed to the following US states: CO, DE, MD, MN, NC, NV, and WV. The products were distributed to the following foreign countries: Canada.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Colorado, Delaware, Maryland, Minnesota, Nevada, North Carolina, West Virginia.
Recall timeline
FDA terminated this recall 9 months after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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-1566-2020 (March 6, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1566-2020 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 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.