Gauze/Sponge, Internal
FDA product code EFQ · Class U · 19 devices · 57 reports · 3 devices named in recalls
- McKesson 61-59120Mckesson Medical-Surgical Inc. · Gauze/Sponge, Internal1 recall0 reports
- McKesson 61-59220Mckesson Medical-Surgical Inc. · Gauze/Sponge, Internal1 recall0 reports
- McKesson 61-59320Mckesson Medical-Surgical Inc. · Gauze/Sponge, Internal1 recall0 reports
- DeRoyal 30-054Deroyal Industries, Inc. · GAUZE/SPONGE, INTERNAL16 reports
- DeRoyal 30-057Deroyal Industries, Inc. · GAUZE/SPONGE, INTERNAL11 reports
- DeRoyal 30-060Deroyal Industries, Inc. · GAUZE/SPONGE, INTERNAL5 reports
- DeRoyal 30-068Deroyal Industries, Inc. · GAUZE/SPONGE, INTERNAL4 reports
- PILLING IPN004227Teleflex Incorporated · GAUZE/SPONGE, INTERNAL4 reports
- DeRoyal 30-055Deroyal Industries, Inc. · GAUZE/SPONGE, INTERNAL3 reports
- DeRoyal 30-154Deroyal Industries, Inc. · GAUZE/SPONGE, INTERNAL3 reports
- DeRoyal 30-301Deroyal Industries, Inc. · GAUZE/SPONGE, INTERNAL2 reports
- MEROCEL® 400402Medtronic Xomed, Inc. · GAUZE/SPONGE, INTERNAL2 reports
- DeRoyal 30-059Deroyal Industries, Inc. · GAUZE/SPONGE, INTERNAL1 report
- DeRoyal 30-303Deroyal Industries, Inc. · GAUZE/SPONGE, INTERNAL1 report
- DeRoyal 30-300Deroyal Industries, Inc. · GAUZE/SPONGE, INTERNAL1 report
- DeRoyal 30-056Deroyal Industries, Inc. · GAUZE/SPONGE, INTERNAL1 report
- PILLING IPN004225Teleflex Incorporated · GAUZE/SPONGE, INTERNAL1 report
- Curity 7831Cardinal Health, Inc. · GAUZE/SPONGE, INTERNAL1 report
- MEROCEL® 470530Medtronic Xomed, Inc. · GAUZE/SPONGE, INTERNAL1 report