Z-0090-2022Class I

EcoGel 100 - RED Medical Supplies Green Ultrasound Gel, Model No. 250UG-GLU

Name: Z-0090-2022 EcoGel 100 - RED Medical Supplies Green Ultrasound Gel, Model No. 250UG-GLU
Creator: Red Medical Supplies
Published: 2021-08-11
License: https://open.fda.gov/license/

Red Medical Supplies / initiated 2021-08-11 / Open, Classified / root cause: manufacturing process

FDA source

Red Medical Supplies began a recall of EcoGel 100 - RED Medical Supplies Green Ultrasound Gel, Model No. 250UG-GLU on 2021-08-11. FDA classified it as Class I and gives the reason as "Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may contain bacterial contamination. On August 18, 2021,FDA published a Letter to Health Care Providers to further address this issue...". As of 2026-09-10, the recall status on record is Open, Classified, and MDM tags the root cause as manufacturing process.

Recall record

Recall number: Z-0090-2022
Classification: Class I
Status: Open, Classified
Initiated: 2021-08-11
Posted: 2021-10-14
Recalling firm: Red Medical Supplies
Product: EcoGel 100 - RED Medical Supplies Green Ultrasound Gel, Model No. 250UG-GLU
Product code: ITX Transducer, Ultrasonic, Diagnostic
Reason for recall: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may contain bacterial contamination. On August 18, 2021,FDA published a Letter to Health Care Providers to further address this issue: https://www.fda.gov/medical-devices/letters-health-care-providers/stop-using-all-eco-med-ultrasound-gels-and-lotions-due-risk-bacterial-contamination-letter-health.
Root cause tag: manufacturing process
FDA root cause: Process control
Action: According to the firm, Amazon.com has issued recall notification to all customers via email. Customers were instructed to return the product as soon as possible. An automatic refund has been issued by Amazon.com as soon as the product was recalled. Amazon.com is in charge of the disposal.
Quantity in commerce: 639
Distribution: Firm sold product through Amazon.com. Domestic distribution nationwide.
Product codes and lots: All product manufactured by Eco-Med between 2020.09.23 - 2021.08.08

Enforcement reports

One row per recalled product line

FDA enforcement reports joined to recall event Z-0090-2022
Recall number	Class	Status	Voluntary or mandated	Report date	Classified
Z-0088-2022	Class I	Ongoing	Voluntary: Firm initiated	2021-10-20	2021-10-13
Z-0089-2022	Class I	Ongoing	Voluntary: Firm initiated	2021-10-20	2021-10-13
Z-0090-2022	Class I	Ongoing	Voluntary: Firm initiated	2021-10-20	2021-10-13

Product code ITX

K961757Class IIEcogel 100 Ultrasound GelEco-Med Pharmaceuticals, Inc. / cleared 1996-07-25

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)