Skip to content
Lower risk Medical device recall · FDA · Published August 18, 2021

Scrip Ultrasound Gel Clear Recall: Bacterial Contamination Risk

Scrip Inc recalls 5L Ultrasound Gel Clear due to potential bacterial contamination. Affected units have an older logo indicating Canadian manufacture. Consumers should check product details to determine if recalled.

🇺🇸 FDA recall #Z-0224-2022Medical deviceScrip ›
Take action

Contact the company

Recalling firmScrip Inc9005 N Industrial Rd · Peoria, IL 61615-1511
✎ GovInfoNow plain-language explainer

Scri: 5L Ultrasound Gel Clear has been recalled because it may contain bacterial contamination. This poses a health risk to users during medical procedures, especially if the gel is used without proper sterilization. Read more at govinfonow.com/recall/61927-scrip-ultrasound-gel-clear-recall-bacterial-contamination-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/61927-scrip-ultrasound-gel-clear-recall-bacterial-contamination-risk · Updated August 19, 2026 · FDA enforcement record: FDA #Z-0224-2022

Cite this page

“Scrip Ultrasound Gel Clear Recall: Bacterial Contamination Risk.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/61927-scrip-ultrasound-gel-clear-recall-bacterial-contamination-risk. Based on FDA recall #Z-0224-2022 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0224-2022%22&limit=1).

The FDA announced on 2021-08-18 that Scrip Inc is recalling Scrip Ultrasound Gel Clear, 5L due to potential bacterial contamination from manufacturer Eco-Med Pharmaceutical, Inc., according to the FDA.

How to tell if you have it

  • Brand: Scrip
  • Product: Scrip Ultrasound Gel Clear, 5L
  • Item Number: 663 0061
  • Distribution: US Nationwide Distribution to all 50 states

The hazard

Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may contain bacterial contamination, according to the FDA.

Context

GovInfoNow's records show other recent recalls of similar products include Sheathes3D Viral Barrier Ultrasound Probe Covers Recall: Infection Risk (2025-11-17), AVID Medical Halyard IV Start Kit Non-Sterile Recall: Risk of Contamination (2026-07-14), and Medline Sterile Saline Wound Wash Recall: Risk of Contamination (2026-01-05).

How to tell if you have this one

Check for the older logo on the product, which indicates it was manufactured by Eco-Med Pharmaceuticals in Canada. The item number is 663 0061 for the recalled units.

  • Brand
    Scrip
  • 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 I
  • Status
    Ongoing
  • Distribution
    US Nationwide Distribution to all 50 states.
Recall numberProduct, codes & lots
Z-0224-2022Scrip Ultrasound Gel Clear, 5L Intended for use in acoustic coupling of ultrasound transducer to tissue; Item Number: 663 0061, all lots bearing old style logo. Older logo states that product was manufactured by Eco-Med Pharmaceuticals in Canada.
Z-0225-2022Scrip Creme All Purpose Lotion Intended for use in acoustic coupling of ultrasound transducer to tissue; Item Number: 663 0019, all lots distributed between August 2018 and August 2021
Based on the official FDA remedy

What to do — step by step

  1. Check Product Details

    Look for the older logo indicating Canadian manufacture and item number 663 0061 to confirm if the product is recalled.

Where it went and when

Where it was distributed

Distributed nationwide.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

FDA distribution: “US Nationwide Distribution to all 50 states.” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA published this recall 3 months after the firm started it.

1. Firm started the recall: Aug 18, 202112. FDA classified it Class I: Nov 17, 202123. Published in FDA’s Enforcement Report: Nov 24, 202132021
  1. Firm started the recall
  2. FDA classified it Class I
  3. Published in FDA’s Enforcement Report

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

Similar recalls

Latest medical device recalls

Keep exploring

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-0224-2022 (August 18, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0224-2022 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.
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