Recalls affecting North Dakota
Notices that name North Dakota in their distribution area, plus every nationwide recall — nationwide recalls reach North Dakota too.
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Class II · 9 months ago
Brand Name: EDAN Product Name: Patient Monitor Model/ recall: As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA
As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA Letter) regarding potential cybersecurity issues with various of the firm…
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Class II · 9 months ago
Community Products, LLC Rifton Equipment, E-Pacer. Model/ recall: Potential for fraying on the body support strap
Potential for fraying on the body support strap.
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Class II · 9 months ago
Tyber Medical Brand Name: VOLT" Wrist Treatment System Product Name: 2.4/2.7 2Column recall: The supplier manufactured anatomical left plates with an incorrect thread
The supplier manufactured anatomical left plates with an incorrect thread orientation.
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Class II · 9 months ago
Merit Medical , Custom Waste Management Kit Vascular Tray REF recall: Inflation device handle may detach from the syringe during procedure
Inflation device handle may detach from the syringe during procedure.
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Class II · 9 months ago
Merit Medical , Custom Manifold Kit REF: K09-13203A recall: Inflation device handle may detach from the syringe during procedure
Inflation device handle may detach from the syringe during procedure.
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Class II · 9 months ago
Community Products, LLC Rifton Equipment, TRAM. Model/ recall: Potential for fraying on the body support strap
Potential for fraying on the body support strap.
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Class II · 9 months ago
Ge Medical Systems Israel, Functional Imaging GE Healthcare Omni Legend recall: There is a potential intermittent issue on certain Omni Legend systems
There is a potential intermittent issue on certain Omni Legend systems that can result in a streaking artifact in the PET clinical scan images. This…
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Class II · 9 months ago
Brand Name: EDAN Product Name: Patient Monitor Model/ recall: As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA
As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA Letter) regarding potential cybersecurity issues with various of the firm…
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Class II · 9 months ago
ICU Medical recall: Plum Solo and Duo Infusion pumps include a feature
Plum Solo and Duo Infusion pumps include a feature, that when selected, automatically flushes the downstream line after a piggyback therapy. The…
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Class II · 9 months ago
ICU Medical, Inc. Tego Connector: REF: 011-D1000, 01C-D1000, 055-D1000, D1000 recall: Needle free access device intended as accessory to vascular access used
Needle free access device intended as accessory to vascular access used in hemodialysis or accessory to intravascular administration sets has a…
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Class II · 9 months ago
ICU Medical Plum Duo Infusion Pump, List Numbers: 400020401 , 400021001 recall: Plum Solo and Duo Infusion pumps include a feature
Plum Solo and Duo Infusion pumps include a feature, that when selected, automatically flushes the downstream line after a piggyback therapy. The…
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Class II · 9 months ago
Brand Name: EDAN Product Name: Patient Monitor Model/ recall: As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA
As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA Letter) regarding potential cybersecurity issues with various of the firm…
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Class II · 9 months ago
Brand Name: EDAN Product Name: Telemetry Transmitter Model/ recall: As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA
As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA Letter) regarding potential cybersecurity issues with various of the firm…
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Class II · 9 months ago
Merit Medical Inflation Device.basixCompak.30 atm/bar.20 mL Reference recall: Inflation device handle may detach from the syringe during procedure
Inflation device handle may detach from the syringe during procedure.
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Class II · 9 months ago
Brand Name: EDAN Product Name: Vital Signs Monitor Model/ recall: As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA
As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA Letter) regarding potential cybersecurity issues with various of the firm…
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Class II · 9 months ago
Brand Name: EDAN Product Name: Central Monitoring System Model/ recall: As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA
As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA Letter) regarding potential cybersecurity issues with various of the firm…
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Class II · 9 months ago
Merit Medical Systems, Inc. Allwell recall: Inflation device handle may detach from the syringe during procedure
Inflation device handle may detach from the syringe during procedure.
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Class II · 9 months ago
Brand Name: EDAN Product Name: Vital Signs Monitor Model/ recall: As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA
As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA Letter) regarding potential cybersecurity issues with various of the firm…
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Class II · 9 months ago
Brand Name: EDAN Product Name: Fetal Monitor Model/ recall: As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA
As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA Letter) regarding potential cybersecurity issues with various of the firm…
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Class II · 9 months ago
Specialty Process Labs LLC Thyroid, USP recall: Subpotent Drug
Subpotent Drug
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Class II · 9 months ago
Graviti Pharmaceuticals Private Limited Furosemide Tablets, USP 40 mg, 1,000 Tablets recall: Presence of Foreign Substance
Presence of Foreign Substance
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Class II · 9 months ago
Zydus Pharmaceuticals Inc Icosapent Ethyl capsules, 1 gram, 120-count bottles recall: Subpotent Drug: Due to oxidation caused by leakage of the contents
Subpotent Drug: Due to oxidation caused by leakage of the contents of the capsules
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Class III · 9 months ago
Cipla USA, Inc. Diclofenac Sodium Topical Gel, 1% recall: Failed PH Specifications
Failed PH Specifications
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NHTSA safety recall · 9 months ago
Kia recall: Due to a software error, the instrument panel display may fail
Due to a software error, the instrument panel display may fail. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle…