Recalls published in August 2026
Everything the FDA, USDA FSIS, CPSC and NHTSA announced in August 2026, newest first.
-
Class II · 2 months ago
Spacelabs Healthcare, Inc. Brand Name: Xhibit Product Name: Xhibit Central Station recall: Due to off-the-shelf display port component that has audio/video failures
Due to off-the-shelf display port component that has audio/video failures
-
Class II · 2 months ago
W L Gore & Associates, Inc. Gore Viabil Short Wire Biliary Endoprosthesis recall: 10 mm diameter x 7 cm with transmural drainage holes (VSWVH1006) incorrectly
10 mm diameter x 7 cm with transmural drainage holes (VSWVH1006) incorrectly labeled as 10 mm diameter x 10 cm length devices without transmural…
-
Class II · 2 months ago
Cardinal Health Presource Kits: 1) Newnan SMR Pack recall: Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled
Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.
-
Class II · 2 months ago
Straumann recall: Bone Level Tapered (BLT) Implant, D 4.1mm RC, SLActive 14mm, Roxolid
Bone Level Tapered (BLT) Implant, D 4.1mm RC, SLActive 14mm, Roxolid, Loxim may inadvertently contain implants that are 12mm in length instead of…
-
Class II · 2 months ago
Covidien, LP V-Loc 90 Absorbable Wound Closure Device Vloc 90 0 VL 22 GS-21 recall: Product may contain a perforation or tear in the sterile barrier packaging
Product may contain a perforation or tear in the sterile barrier packaging. This issue may result in biocontamination of the sterile sutures, which…
-
Class II · 2 months ago
Erbecryo 2 Cryosurgical Unit Model/ recall: A strong pull on the high-pressure transfer hose of cryosurgical unit
A strong pull on the high-pressure transfer hose of cryosurgical unit may lead to pneumatic short circuit between he gas inlet and the connector…
-
Class II · 2 months ago
Philips Azurion, Model Numbers: 722229, 722230, 722231, 722232 recall: Two software related issues: 1) Potential image quality degradation
Two software related issues: 1) Potential image quality degradation that may lead to delay of therapy, procedural complications and/or inappropriate…
-
Class II · 2 months ago
Remel Europe Ltd. Thermo Fisher Diagnostics Neisseria meningitidis Gp C 2ml/VL recall: Certain lots of Neisseria meningitidis Gp C 2ml/VL, R30166901
Certain lots of Neisseria meningitidis Gp C 2ml/VL, R30166901, are not performing to IFU criteria not positive to ATCC13102 within 60 Seconds.
-
Class II · 2 months ago
Medline Micro-Kill Bleach Germicidal Bleach Wipes,7" x 8" recall: Medline Micro-Kill Bleach Germicidal Bleach Wipes may exhibit a reduction
Medline Micro-Kill Bleach Germicidal Bleach Wipes may exhibit a reduction in bleach concentration to levels below specification prior to the end of…
-
Class II · 2 months ago
Cardinal Health Presource Kits: 1) CHI STD Neuro Crani OPT 2 recall: Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled
Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.
-
Class II · 2 months ago
Ventana Medical Systems, Inc. navify Digital Pathology v2.5 recall: Due to complaints received for the Image Management System regarding
Due to complaints received for the Image Management System regarding image/metadata discrepancy with the Viewer window
-
Class II · 2 months ago
Cardinal Health Presource Kits: 1) FAT GRAFT ADD KIT recall: Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled
Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.
-
Class II · 2 months ago
Covidien, LP Surgipro II S8698GX Surgipro II BL 5/0 18 P-13 S8698GX recall: Product may contain a perforation or tear in the sterile barrier packaging
Product may contain a perforation or tear in the sterile barrier packaging. This issue may result in biocontamination of the sterile sutures, which…
-
Class II · 2 months ago
Galt Medical Corporation Boston Scientific Enhance Transcarotid/Peripheral Access Kit recall: Black depth markings may detach from the outer sheath of the coaxial dilator
Black depth markings may detach from the outer sheath of the coaxial dilator introducer component of transcarotid-peripheral access kits.
-
Class I · 2 months ago
Baxter Duo-Vent Solution Set and Male Luer Lock Adapter recall: Baxter received customer reports of air bubbles in the drip chamber
Baxter received customer reports of air bubbles in the drip chamber and tubing when a pressure cuff is in use or when the tubing is flushed at the…
-
Class I · 2 months ago
Brand Name: Elevaris/Spectra Medical Devices Product Name: Sodium recall: Manufacturing firm, Huons, was cited for issues regarding product quality
Manufacturing firm, Huons, was cited for issues regarding product quality and sterility assurance. If the product sterility is compromised, patients…
-
Class II · 2 months ago
Medline Micro-Kill Bleach Germicidal Bleach Wipes, 6" x 5" recall: Medline Micro-Kill Bleach Germicidal Bleach Wipes may exhibit a reduction
Medline Micro-Kill Bleach Germicidal Bleach Wipes may exhibit a reduction in bleach concentration to levels below specification prior to the end of…
-
Class II · 2 months ago
Medline Micro-Kill Bleach Germicidal Bleach Wipes, 12" x 12" recall: Medline Micro-Kill Bleach Germicidal Bleach Wipes may exhibit a reduction
Medline Micro-Kill Bleach Germicidal Bleach Wipes may exhibit a reduction in bleach concentration to levels below specification prior to the end of…
-
Class II · 2 months ago
Terumo Medical Corporation Glidesheath Slender A-Kit 6F 10CM .021GW. 5 units per box recall: Product was packaged with the 0.025 guidewire instead of the 0.021 guidewire
Product was packaged with the 0.025 guidewire instead of the 0.021 guidewire.
-
Class II · 2 months ago
Philips Medical Systems Nederland B.v. Allura Xper FD. Model Numbers: 722026 recall: Firmware issue potentially leading to loss of geometry movements
Firmware issue potentially leading to loss of geometry movements.
-
Class II · 2 months ago
Cardinal Health Presource Kits: 1) KIT, MER Neuro Back recall: Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled
Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.
-
Class II · 2 months ago
Medline Micro-Kill Bleach Germicidal Bleach Wipes, 12" x 12" recall: Medline Micro-Kill Bleach Germicidal Bleach Wipes may exhibit a reduction
Medline Micro-Kill Bleach Germicidal Bleach Wipes may exhibit a reduction in bleach concentration to levels below specification prior to the end of…
-
Class II · 2 months ago
Cardinal Health Presource Kits: 1) Harmonized Spine VCH PHC Pack recall: Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled
Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.
-
Class II · 2 months ago
Microvention Inc. Bobby Balloon Guide Catheter REF: BOB-895-CN BOB-895-Emea recall: Due to an increase rate of balloon pinhole defects
Due to an increase rate of balloon pinhole defects.