co_sos
1 records
fda
4 records
FDA Recall: DJO, LLC — Class II
20260520
Due to broken connector which may result in a temporary interruption of prescribed cold therapy. | Product: Brand Name: DONJOY Product Name: ICEMAN W/,UNIV,LOOP,NS,EH Model/Catalog Number: 11-1424 ...
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FDA Device Recall: Cold Form Wrap: Back, REF: DP163CT03-BLK-L,XL, and Shoulder, REF: DP163CT02
2025-12-03
Class II — 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...
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FDA Device Recall: Ultra-Myossage Lotion 1-gallon bottle, REF: 4262; Myossage Lotion 1-gallon bott
2021-10-13
Class I — 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 a...
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FDA Device Recall: Aircast REF 3011 - PL RX only VF-PL Sterile Cuff Pkg., Lot# 418003, Expiration
2019-07-24
Class II — The product may not meet sterility requirements. Product labeled as sterile, however all units do not appear to meet sterility requirements.
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nppes
1 records
ny_corps
2 records
NY Corp: DJO ASSOCIATES, LLC
2020-04-17
FOREIGN LIMITED LIABILITY COMPANY | County: New York | Jurisdiction: Delaware
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NY Corp: DJO, LLC
2016-03-15
DOMESTIC LIMITED LIABILITY COMPANY | County: Queens | Jurisdiction: New York
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