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All product recalls associated with OEC Medical Systems, Inc.
Total Recalls
1000
Past Year
1000
Class I (Serious)
34
Most Recent
Jan 2026
Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.
Secondary collimator filters may be missing on certain x-ray units. It was discovered that the secondary collimator filter on some OEC 9600 C-arms was omitted when a collimator assembly was replaced. This would reduce the filtration and therefore the Half-Value-Layer (HVL) of the X-ray beam, and may result in non-compliance with respect to Maximum Entrance Exposure Rate (EER) unless the maximum EE
This recall involves the SunRinglé Hollow Quick Release Devices for bicycles and includes models Hollow CroMo Front 100mm, Hollow CroMo Rear 130mm, and Hollow CroMo Rear 135mm. These devices have hollow skewers. They were sold individually or with SunRinglé front and rear wheels with model names Black Flag, Disc o Flea, Charger, STR8 Track, Accelerator R3.00C and Accelerator T3.0C. "Ringlé" is stamped on the lever. Quick release devices with a solid skewer are not included in this recall.
Failure to of affected units to comply with EER/AKR limits due to misinterpretation of the measurement requirements specified in 21 CFR 1020.32 (d) (3) (iii)