Recall archive
59 recalls · page 3 of 3
Reported Jul 31, 2019
Monoject Standard Hypodermic Needle, 14 G x 1-1/2" Item code: 8881200011
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cardinal Health 200, LLC
Matched: Brand — Manufacturing defect was found for the cartridge component, which could compromise the sterility barrier of the product
16 more products in this recall
FDA (openFDA device enforcement)
Reported May 15, 2019
ChemoPlus Chemo Spill Kit Product Code:CT4004 Product Usage: ChemoPlus chemotherapy spill kits are for the clean-up and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cardinal Health 200, LLC
Matched: Brand — Kit label states not made with natural rubber latex,however safety goggles within the kits contain natural rubber latex in the goggle strap
3 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 6, 2019
Curity All Purpose Sponges, Non-woven, 4 Ply, 4" x 4" (10.2 cm x 10.2 cm) Product Code: 8044 - Product Usage: Ideal for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cardinal Health 200, LLC
Matched: Brand — Curity All Purpose Sponges were not sterilized and distributed
FDA (openFDA device enforcement)
Reported Dec 26, 2018
Protexis Neoprene Surgical Glove, Size 5.5 This powder-free sterile light brown colored surgeons gloves are a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cardinal Health 200, LLC
Matched: Brand — Labeling issue in that the breakthrough (i.e., permeation) times for two chemotherapy drugs (Carmustine and Thiotepa) stated on the wallet (primary…
7 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 25, 2018
Presource PBDS, Kit, Common Diabetes. Kit includes a exerciser volumetric 5000 ML device, two items of cloth, skin prep…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cardinal Health 200, LLC
Matched: Brand — A defect in the seal of the Gatorade pouch contained in kits caused the pouch to leak within a limited portion of the kit.
14 more products in this recall
FDA (openFDA device enforcement)
Reported May 9, 2018
Medi-Vac(TM) Flex Advantage(TM) Suction Canister Liner, Material Numbers: a) REF 6561-910C b) REF 6561-916K c) REF…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cardinal Health 200, LLC
Matched: Brand · Product details — products may be missing a one-way valve on the fluid patient port.
FDA (openFDA device enforcement)
Reported Sep 13, 2017
Presource(R) Kits (custom surgical/procedural kits): The standard and custom kits are packed with all of the specific…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cardinal Health 200, LLC
Matched: Brand — The firm manufactured and distributed Presource(R) kits which contained BD SafetyGlide" 22GA 1¿ inch Needles. BD subsequently recalled these needles…
FDA (openFDA device enforcement)
Reported Aug 30, 2017
Convertors Robotic Drape with Attached Leggings; Product is packaged as Single Sterile Drape/8 per Case
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cardinal Health 200, LLC
Matched: Brand — Product 29474 LAVH drape was packaged as 29574 Robotic Drape with Leggings.
FDA (openFDA device enforcement)
Reported Aug 2, 2017
Converters(R) Under Buttocks Drape with Fluid Control Pouch II, REF 8482, STERILE R, Qty. 1, Cardinal Health, Waukegan,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cardinal Health 200, LLC
Matched: Brand · Product · Product details — Outer label of some units of product number/lot number 8482, Lot 16LFS235 and product number/lot number 9414, Lot 16LUS317 do not match the drape…
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 31, 2017
Jackson-Pratt Hemaduct Cardiothoracic Silicone Round Drain,19FR. Sterile, Rx Only. For Single Use Only. Jackson-Pratt…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cardinal Health 200, LLC
Matched: Brand — Product's seal possibly compromised, potentially compromising the sterility of the package contents. Use of impacted products could result in an…
19 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 19, 2016
V. Mueller Neuro/Spine, SHADOW-LINE, SPINAL DISTRACTION SCREW, STERILE, various sizes (12mm, 14mm, 16mm and 18mm) 5 PER…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cardinal Health 200, LLC
Matched: Brand — Potential risk associated with corrosion demonstrated on the distraction screw surface.
FDA (openFDA device enforcement)
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