DJO recalls 1-gallon Ultra-Myossage Lotion bottles (REFs 4262 and 4210) due to potential bacterial contamination. FDA issued a warning on August 18, 2021.
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.
DJO is recalling 1-gallon Ultra-Myossage Lotion bottles (REFs 4262 and 4210) because they may contain bacteria. Using these products could lead to infections, especially for people with open wounds or compromised immune systems.
The lotions may have bacterial contamination, which can cause infections. This risk is particularly concerning for individuals with open wounds or compromised immune systems, as bacteria can enter the body through the skin.
People who own or use these lotions for physical therapy or self-treatment are affected. Those with open wounds or weakened immune systems are at higher risk.
Check for 1-gallon bottles labeled 'Ultra-Myossage Lotion' with REF numbers 4262 or 4210. These products were sold in DJO kits manufactured by Eco-Med Pharmaceutical, Inc.
Look for the product name and reference numbers on the bottle to confirm if it's part of the recall.
Reach out to DJO directly for specific instructions on what to do with the recalled lotions.
The lotions may contain bacterial contamination, which can lead to infections, especially for people with open wounds or weakened immune systems.
Check for 1-gallon bottles labeled 'Ultra-Myossage Lotion' with reference numbers 4262 or 4210.
Contact DJO directly for specific instructions on what to do with the recalled lotions.
We’ve drafted a message you can send DJO to request your refund or repair — edit it as you like.
Subject: Recall Z-0010-2022 — DJO DJO Hello, I own a DJO that is covered by recall Z-0010-2022 from DJO. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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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.
