DJO, LLC recalls Ultra-Myossage Lotion 1-gallon bottle, REF: 4262; Myossage Lotion 1-gallon bottle, REF: 4210, located in the following DJO, LLC / DJO…
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:…
Read the official notice →- Date
- 2021-10-13
- Country
- United States
- Brand
- DJO
- Product
- Ultra-Myossage Lotion 1-gallon bottle, REF: 4262; Myossage Lotion 1-gallon bottle, REF: 4210, located in the following DJO, LLC / DJO…
- Classification
- Class I
- Units
- Worldwide distribution - U.S. Nationwide distribution including in the states…
- Category
- Drugs & medical
- Source
- FDA · Device
Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer
What to do
- Check the product name, strength and lot number against the official notice.
- Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
- Ask the pharmacy or supplier about a replacement or refund.
General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.
More DJO recalls
- 2026-05-20
USDJO, LLC recalls Brand Name: DONJOY Product Name: ICEMAN W/,UNIV,LOOP,NS,EH Model/Catalog Number: 11-1424 Software Version: No Product Description: 11-1424…
Due to broken connector which may result in a temporary interruption of prescribed cold therapy.
FDA · DeviceDJO, LLCWorldwide - U.S. Nationwide distribution in the states of AK, AL, AZ, CA, CO,…Official notice →- 2025-12-03
- US
DJO, LLC recalls Cold Form Wrap: Back, REF: DP163CT03-BLK-L,XL, and Shoulder, REF: DP163CT02
The IFU (Information for Use) on the wrap instructs the user to heat the hot and cold compression wrap in the microwave for 3 minutes, which may cause the wrap to leak or break at the seams and/or reach temperatures…
FDA · DeviceDJO, LLCUS Nationwide distribution in the states of WI, TN, TX, MD, GA, UT, WA, MI,…Official notice →
Other drugs & medical recalls in the United States
- 2021-10-13
- US
Paltop Advanced Dental Solutions Ltd recalls Scan Abutment SP, Cat. No. 30-70101 - Product Usage: used to take an impression with an intra oral scanner or optical…
Some devices are outside tolerances and showed a maximal deviation of 2 degrees in the orientation between the peek head and titanium base, and an incongruence between the size engraved on the peek has been identified.…
FDA · DevicePaltop Advanced Dental Solutions LtdUS Nationwide distribution. No foreign distribution from US.Official notice → - US
GE Healthcare, LLC recalls Centricity Universal Viewer 7.0, Model 5829628-0XX. Radiological image processing system
A software anomaly exists in the Centricity Universal Viewer study management feature in which study changes are not propagated to either the Centricity Enterprise Archive (EA) or another Vendor Neutral Archive (VNA).
FDA · DeviceGE Healthcare, LLCAR, IL, ME, MS, NE, NJ, NY, and TN Belgium, Canada, Costa Rica, France,…Official notice → - US
Welch Allyn Inc Mortara recalls ELI, Burdick and McKesson brand 280 Resting Electrocardiographs (ELI 280, MLBUR280 and BUR280), Model Numbers: ELI280-DDB-ADAAX,…
The devices malfunction under specific operator workflows.
FDA · DeviceWelch Allyn Inc MortaraDistribution was nationwide, including Puerto Rico. Foreign distribution was…Official notice → - US
Medtronic Perfusion Systems recalls Medtronic Bio-Medicus Insertion Kits, Model number 96553, Pediatric Insertion Kit, Sterile; and Model number 96551, Venous Insertion…
There was a label mix-up between two model numbers resulting in the incorrect guidewire being contained in the kits for both model numbers.
FDA · DeviceMedtronic Perfusion SystemsWorldwide distribution - US Nationwide distribution in the state of…Official notice → - US
Bard Peripheral Vascular Inc recalls REF TIN3015, 15G x 79 mm Bone Marrow Aspiration/Intraosseous Infusion Needle, For Single Use Only, Sterile EO, UDI: 10885403043796
Potential for needle protector to become fully dislodge exposing infusion needle which could result in needle stick.
FDA · DeviceBard Peripheral Vascular IncWorldwide distribution - US Nationwide distribution in the states of AL, AR,…Official notice → - US