Recalls affecting Maryland
Notices that name Maryland in their distribution area, plus every nationwide recall — nationwide recalls reach Maryland too.
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NHTSA safety recall · 2 months ago
Kia EV9 recall: Due to improper routing, the Occupant Detection System (ODS)
Due to improper routing, the Occupant Detection System (ODS) may not deactivate the air bag when a child or child seat is in the front passenger…
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NHTSA safety recall · 2 months ago
Marathon Industries recall: The deck pins may break, resulting in the liftgate platform falling
The deck pins may break, resulting in the liftgate platform falling.
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NHTSA safety recall · 2 months ago
General recall: The rearview camera screen may display a distorted or blank image
The rearview camera screen may display a distorted or blank image.
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Highest risk · 2 months ago
Modine Manufacturing Company Airedale Heating and Cooling Ventilation Fans recall: Fire Hazard
Fire Hazard
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Highest risk · 2 months ago
KTM North America Off-Road Motorcycles recall: Risk of Serious Injury or Death from Crash Hazard
Risk of Serious Injury or Death from Crash Hazard
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Highest risk · 2 months ago
Goal Zero YETI 3000X Power Stations recall: Serious Risk of Injury from Fire and Burn Hazards
Serious Risk of Injury from Fire and Burn Hazards
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Class II · 2 months ago
Biofire Respiratory Panel 2.1 REF 423742 UDI code: 00815381020529 recall: Due to increase in false negative results
Due to increase in false negative results
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Class II · 2 months ago
OBP Medical , ER-Spec Single-Use Vaginal Speculum with LED Light recall: There is a potential for vaginal speculums to contain a burr on the proximal
There is a potential for vaginal speculums to contain a burr on the proximal plastic blade, which may introduce a sharp edge in the contact regions…
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Class II · 2 months ago
Covidien, LP Dermalon 88861757-31 Dermalon* 4-0 BLU 75CM C13 88861757-31 88861799-31 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…
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Class II · 2 months ago
Cardinal Health Presource Kits: 1) Basic 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.
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Class II · 2 months ago
Covidien, LP Surgipro SP-623 Surgipro* 2-0 BLU 75CM SC2 X36 SP-623 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…
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Class II · 2 months ago
Straumann USA LLC GM Helix Implant, Endosseous Dental Implant Article No. 109.984 recall: There may be a mismatch between the implant contained inside the packaging
There may be a mismatch between the implant contained inside the packaging and the information described on the outer carton label. If the the…
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Class II · 2 months ago
Cardinal Health Presource Kits: 1) Septo Rhino 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.
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Class II · 2 months ago
Bd Switzerland Sarl 60 In Non-DEHP Minibore Extension Set RES ME2010 UDI-DI code recall: Products may not have received adequate sterilization processing
Products may not have received adequate sterilization processing.
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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
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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…
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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.
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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…
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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…
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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…
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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.
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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…
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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.
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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