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 · 8 months ago
Waldemar Link GmbH & Co. KG Endo-Model Replacement Plateau recall: The potential for an implant with a plateau screw where the bushing
The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.
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Class II · 8 months ago
Instrumentation Laboratory GEM Premier 5000 recall: Confirmed customer complaints indicating that GEM PAKs (cartridges)
Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control…
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Class II · 8 months ago
International Life Sciences Artelon FlexBand Dynamic Matrix Ref: 31057 recall: Augmentation devices failed bacterial endotoxin testing
Augmentation devices failed bacterial endotoxin testing.
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Class II · 8 months ago
Beckman Coulter Mishima K.K. Chemistry Analyzer AU5800, REF: B96697, B96698 recall: A delay in results may occur. When clinical chemistry analyzer calibration
A delay in results may occur. When clinical chemistry analyzer calibration monitor with PC installed with Microsoft SQL Server 2022 Express is open…
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Class II · 8 months ago
Instrumentation Laboratory GEM Premier 5000 PAK recall: Confirmed customer complaints indicating that GEM PAKs (cartridges)
Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control…
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Class III · 8 months ago
Penner Pacific Bathing Spa, Model Numbers 360020-1P recall: The device does not bear a unique device identifier
The device does not bear a unique device identifier.
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Class II · 8 months ago
Waldemar Link GmbH & Co. KG Endo-Model Replacement Plateau recall: The potential for an implant with a plateau screw where the bushing
The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.
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Class II · 8 months ago
Zydus Pharmaceuticals Inc Icosapent Ethyl Capsules, 1 gram, 120 Capsules per bottle recall: Failed Tablet/Capsule specifications: Red dots inside capsule and melted
Failed Tablet/Capsule specifications: Red dots inside capsule and melted capsule caused by oxidized Icosapent ethyl, the active ingredient.
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NHTSA safety recall · 8 months ago
Ford F-59 and F-53 commercial stripped chassis recall: The exterior brake lights may remain illuminated when the driver
The exterior brake lights may remain illuminated when the driver is not applying the brakes. As such, these vehicles fail to comply with the…
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NHTSA safety recall · 8 months ago
Ford Explorer and Lincoln Aviator recall: The seat belt anchor bolts at the second-row outer seating positions
The seat belt anchor bolts at the second-row outer seating positions may be improperly secured.
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NHTSA safety recall · 8 months ago
Chrysler Jeep Wagoneer S recall: The liftgate hinge cover may not be properly clipped into position
The liftgate hinge cover may not be properly clipped into position and may detach from the vehicle.
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Highest risk · 8 months ago
Stoney Games Kluster Magnet Chess Games recall: Risk of Serious Injury or Death from Magnet Ingestion
Risk of Serious Injury or Death from Magnet Ingestion; Violates Mandatory Standard for Toys
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Highest risk · 8 months ago
ProRider Bicycle Helmets recall: Risk of Serious Injury or Death from Head Injury
Risk of Serious Injury or Death from Head Injury; Violates Mandatory Standard for Bicycle Helmets
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Elevated risk · 8 months ago
Lfte USA Playground Swing Set Seats recall: Fall Hazard
Fall Hazard
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NHTSA safety recall · 8 months ago
Volvo Car EX30 and EX30CC recall: The seat belt warning system may not activate the audible warning chime
The seat belt warning system may not activate the audible warning chime as intended. As such, these vehicles fail to comply with the requirements of…
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NHTSA safety recall · 8 months ago
Volkswagen Jetta recall: The transmission ground wire may not have been properly connected during
The transmission ground wire may not have been properly connected during assembly, causing an open electrical circuit.
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Class II · 8 months ago
Olympus Corporation of the Americas Brand Name: ShockPulse-SE Lithotripsy System recall: Ongoing investigations identified additional instances of the device
Ongoing investigations identified additional instances of the device Generator remaining in a blinking phase waiting to recognize the transducer…
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Class II · 8 months ago
Vascutek, Ltd. Gelsoft Plus, REF: 635024PE, 631514PE, 631222PE, 633008PE recall: Gelatin sealed woven polyester prostheses devices
Gelatin sealed woven polyester prostheses devices, designed for vascular repair, were incorrectly labeled with an additional month of shelf life…
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Class II · 8 months ago
Diagnostica Stago, Inc. Brand Name: STA Liatest Free Protein S Product Name: STA recall: The potential of out-of-range results and an underestimation of the free
The potential of out-of-range results and an underestimation of the free protein S level in normal patient plasmas. The defect only affects…
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Class II · 8 months ago
Olympus Corporation of the Americas Brand Name: ShockPulse-SE Lithotripsy System recall: Ongoing investigations identified additional instances of the device
Ongoing investigations identified additional instances of the device Generator remaining in a blinking phase waiting to recognize the transducer…
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Class II · 8 months ago
B Braun Medical Inc Brand Name: B. Braun Product Name: BBraun Medical 21G X4.4CM recall: The potential for the needle tip to be dull/blunt
The potential for the needle tip to be dull/blunt, difficult to advance, and/or break.
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Class II · 8 months ago
B Braun Medical Inc Brand Name: B. Braun Product Name: 21GA Winged Infusion recall: The potential for the needle tip to be dull/blunt
The potential for the needle tip to be dull/blunt, difficult to advance, and/or break.
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Class II · 8 months ago
Datascope Corp. CS100 Iabp. Software Version CS100 Iabp Q.01 recall: The firm has identified that the battery runtime and cycle specifications
The firm has identified that the battery runtime and cycle specifications contained in the devices Instructions for Use (IFU) need to be updated.
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Class II · 8 months ago
Siemens Healthcare Diagnostics, Inc. Atellica CH Urine Albumin . Material Number recall: Falsely depressed UAlb patient results may occur. Affected samples with any
Falsely depressed UAlb patient results may occur. Affected samples with any urine albumin concentration above the UAlb measuring interval >40.0 mg/dL…