Recalls affecting New Mexico
Notices that name New Mexico in their distribution area, plus every nationwide recall — nationwide recalls reach New Mexico too.
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Class II · 5 months ago
Kico Knee Innovation Company Arvis Hip & Knee 2.0 Instrument Set recall: The Impactor V-Block Assembly and Trackers A, B
The Impactor V-Block Assembly and Trackers A, B, C and E may exhibit signs of early wear and/or corrosion on the exposed magnet face.
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Class II · 5 months ago
Covidien Mon-a-Therm Esophageal Stethoscope with Temperature Sensor recall: Temperature probe devices lack FDA clearance
Temperature probe devices lack FDA clearance.
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Class II · 5 months ago
Covidien Mon-a-Therm General Purpose recall: Temperature probe devices lack FDA clearance
Temperature probe devices lack FDA clearance.
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Class II · 5 months ago
CareFusion 303, Inc. BD Pyxis MedStation 4000 REF: 303 Medication cabinet recall: Fingerprint scanner may overheat to a temperature to cause 1st degree burn
Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
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Class II · 5 months ago
DeRoyal Industries Inc. Ref 46-406, Covaderm Plus recall: Sterile wound dressing, lacks sterility assurance
Sterile wound dressing, lacks sterility assurance
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Class II · 5 months ago
SSC- Surgical Specialties Corporation Sharpoint 2.2MM, Angled, Double- Bevel Model/ recall: 3.0mm surgical knives labeled and packaged as 2.2mm surgical knives
3.0mm surgical knives labeled and packaged as 2.2mm surgical knives.
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Class II · 5 months ago
Shimadzu Medical Systems Digital Angiography System Trinias:UD150G-40 / D150GC-40 recall: Electromagnetic contactors within high voltage generator may weld together
Electromagnetic contactors within high voltage generator may weld together, resulting in current being supplied to power supply even if power is off.
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Class II · 5 months ago
CareFusion 303, Inc. BD Pyxis Anesthesia Station ES REF: 327 Medication cabinet recall: Fingerprint scanner may overheat to a temperature to cause 1st degree burn
Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
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Class II · 5 months ago
Fresenius Kabi USA, LLC The Large Volume Pump of the Ivenix Infusion System recall: Potential for the Cassette Loading Lever to break
Potential for the Cassette Loading Lever to break.
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Class I · 5 months ago
Becton Dickinson & Company BD¿Spinal Tray with BD¿Quincke Needle 22 G x 3.5 recall: This is a sub-recall of a product recall from Huons Co, Ltd
This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is…
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Class I · 5 months ago
Becton Dickinson & Company BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 recall: This is a sub-recall of a product recall from Huons Co, Ltd
This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is…
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Class I · 5 months ago
Becton Dickinson & Company BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 recall: This is a sub-recall of a product recall from Huons Co, Ltd
This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is…
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Class I · 5 months ago
B Braun Medical Inc Spinal Needle procedure kits: Material Description 24GA. Pencan recall: These procedure kits contain Bupivacaine Hydrochloride in Dextrose Injection
These procedure kits contain Bupivacaine Hydrochloride in Dextrose Injection, USP. The manufacturer of the Bupivacaine, Huons Co, Ltd., has issued a…
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Class II · 5 months ago
Oculus Technologies of Mexico, S.A. de C.V. PhaseOne Antimicrobial Solution, Model/ recall: The recall is being conducted due to corrosion of the internal metallic
The recall is being conducted due to corrosion of the internal metallic spring within the sprayer component. This condition is caused by material…
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Class I · 5 months ago
Becton Dickinson & Company BD¿Spinal Tray with BD¿Quincke Needle 25 G x 3.5 recall: This is a sub-recall of a product recall from Huons Co, Ltd
This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is…
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Class I · 5 months ago
Becton Dickinson & Company BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 recall: This is a sub-recall of a product recall from Huons Co, Ltd
This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is…
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Class II · 5 months ago
Grace Medical, Inc. Titanium/Fluoroplastic Piston 0.6MM DIA X 3.75MM L Model/ recall: Due to incorrect functional length on device labeling
Due to incorrect functional length on device labeling.
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Class II · 5 months ago
Philips Azurion 7M20, Model Numbers: 722079 recall: During the device phase of Roadmap Pro, a user may experience a dark image
During the device phase of Roadmap Pro, a user may experience a dark image that is not clinically usable. The dark image may result after the user…
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Class II · 5 months ago
Philips Azurion 5M20, Model Numbers: 722228 with Software release recall: During the device phase of Roadmap Pro, a user may experience a dark image
During the device phase of Roadmap Pro, a user may experience a dark image that is not clinically usable. The dark image may result after the user…
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Class II · 5 months ago
B Braun Medical Inc Brand Name: B. Braun Medical INC. Product Name: Bpsk recall: B. Braun was notified by our supplier, Ferndale Laboratories, Inc
B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL¿ Liquid Adhesive, that they have issued a voluntary…
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Class II · 5 months ago
CareFusion 303, Inc. BD Pyxis MedStation ES REF: 323 Medication cabinet recall: Fingerprint scanner may overheat to a temperature to cause 1st degree burn
Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
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Class II · 5 months ago
Philips Azurion 7M12, Model Numbers: 722078 recall: During the device phase of Roadmap Pro, a user may experience a dark image
During the device phase of Roadmap Pro, a user may experience a dark image that is not clinically usable. The dark image may result after the user…
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Class II · 5 months ago
Covidien Shiley Tracheostomy Tube Cuffed with Inner Cannula REF 6FEN recall: Due to customer complaint regarding incorrect display box labeling
Due to customer complaint regarding incorrect display box labeling.
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Class II · 5 months ago
B Braun Medical Inc Brand Name: B. Braun Medical INC. Product Name: NES1725Kfxl recall: B. Braun was notified by our supplier, Ferndale Laboratories, Inc
B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL¿ Liquid Adhesive, that they have issued a voluntary…