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Pajunk Recalls
1 recall on record · November 6, 2019 to November 6, 2019 · Medical Devices
November 6, 2019
Medical Devices
FDA
Pajunk GmbH recalls SPROTTE Lumbar with Introducer, labeled as the following: 1. Sprotte 22G x 90mm w/ introducer and wings (25/box);
Hazard: Problem with packaging sealing process which affects sterility.
Pajunk Recalls | RecallWatchUSA