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 · 1+ years ago
Integra LifeSciences Corp. Brand Name: MediHoney ¿ Product Name: MediHoney¿ Paste recall: Packaging failures were identified which could lead to a breach
Packaging failures were identified which could lead to a breach in the sterile barrier.
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Class I · 1+ years ago
Brand Name: Dexcom G7 Continuous Glucose Monitoring System Product recall: The affected devices are the Dexcom G7 Continuous Glucose Monitoring System
The affected devices are the Dexcom G7 Continuous Glucose Monitoring System (CGM System) using iOS, watchOS and Android App software (versions 2.8.0…
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Class II · 1+ years ago
Raysearch Laboratories Ab RayStation with the following product descriptions: 1 recall: DICOM SOP Instance UID and Series Instance UID from RayGateway
DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the interface to Accuray's iDMS, are not guaranteed to be unique.
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Class II · 1+ years ago
Raysearch Laboratories Ab RayStation with the following product descriptions: 1 recall: DICOM SOP Instance UID and Series Instance UID from RayGateway
DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the interface to Accuray's iDMS, are not guaranteed to be unique.
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Class II · 1+ years ago
Lumicell, Inc. Brand Name: 900-00218 Sterile Cover 10-Pack Shipper Box Assembly recall: The potential of the elastic bands included in the kit detaching
The potential of the elastic bands included in the kit detaching or fracturing during surgical procedures. As a result, these failures may pose a…
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Class II · 1+ years ago
Visgeneer, Inc. Blood Uric Acid Monitoring System Each kit contains 1 meter recall: Due to products distributed without premarket clearance or approvals
Due to products distributed without premarket clearance or approvals.
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Class I · 1+ years ago
Medtronic Perfusion Systems DLP Left Heart Vent Catheter Malleable body and vented recall: The catheters may not retain their shape
The catheters may not retain their shape.
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Class I · 1+ years ago
mo-Vis BVBA IDM-MICRO-R. Electrical wheelchair component recall: Devices with firmware versions 2.3 and lower may experience timing variations
Devices with firmware versions 2.3 and lower may experience timing variations between software tasks, which could result in skipping the necessary…
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Class II · 1+ years ago
Semaglutide, 2.5 mg/mL injection, 4 mL, Boothwyn Pharmacy recall: Subpotent Drug
Subpotent Drug
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Class II · 1+ years ago
Immunocore, LLC Kimmtrak Injection, 100 mcg/0.5 mL, For intravenous Infusion After recall: Subpotent Drug
Subpotent Drug
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Class II · 1+ years ago
Semaglutide, 2.5 mg/mL injection, 2 mL., Boothwyn Pharmacy recall: Subpotent Drug
Subpotent Drug
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Class II · 1+ years ago
Amneal Pharmaceuticals, LLC chlorproMazine Hydrochloride Tablets, USP recall: Presence of a foreign substance.A specific lot of auxiliary polyester coil
Presence of a foreign substance.A specific lot of auxiliary polyester coil, used in product packaging was detected with presence of a micro-organism…
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Class I · 1+ years ago
DermaRite Industries, LLC KleenFoam, Antimicrobial Foam Soap with Aloe Vera recall: Microbial Contamination of Non-Sterile Drug Product: The products were found
Microbial Contamination of Non-Sterile Drug Product: The products were found to be contaminated with the bacteria Burkholderia cepecia.
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Class II · 1+ years ago
Amneal Pharmaceuticals, LLC Sulfamethoxazole and Trimethoprim Tablets, USP 800mg/160mg recall: Presence of a foreign substance.A specific lot of auxiliary polyester coil
Presence of a foreign substance.A specific lot of auxiliary polyester coil, used in product packaging was detected with presence of a micro-organism…
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Class I · 1+ years ago
DermaRite Industries, LLC DermaKleen, Health Care Antiseptic Lotion Soap with Vitamin recall: Microbial Contamination of Non-Sterile Drug Product: The products were found
Microbial Contamination of Non-Sterile Drug Product: The products were found to be contaminated with the bacteria Burkholderia cepecia.
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Class II · 1+ years ago
Amneal Pharmaceuticals, LLC chlorproMazine Hydrochloride Tablets, USP recall: Presence of a foreign substance.A specific lot of auxiliary polyester coil
Presence of a foreign substance.A specific lot of auxiliary polyester coil, used in product packaging was detected with presence of a micro-organism…
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Class II · 1+ years ago
Amneal Pharmaceuticals, LLC chlorproMazine Hydrochloride Tablets, USP recall: Presence of a foreign substance.A specific lot of auxiliary polyester coil
Presence of a foreign substance.A specific lot of auxiliary polyester coil, used in product packaging was detected with presence of a micro-organism…
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Class II · 1+ years ago
Amneal Pharmaceuticals, LLC chlorproMazine Hydrochloride Tablets, USP recall: Presence of a foreign substance.A specific lot of auxiliary polyester coil
Presence of a foreign substance.A specific lot of auxiliary polyester coil, used in product packaging was detected with presence of a micro-organism…
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Class III · 1+ years ago
Fluorescein 2% Ophth, 3 ML, Boothwyn Pharmacy, 800-476-7496 recall: Subpotent Drug
Subpotent Drug
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Class I · 1+ years ago
DermaRite Industries, LLC DermaSarra, External Analgesic, 222 mL per bottle recall: Microbial Contamination of Non-Sterile Drug Product: The products were found
Microbial Contamination of Non-Sterile Drug Product: The products were found to be contaminated with the bacteria Burkholderia cepecia.
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Class I · 1+ years ago
DermaRite Industries, LLC PeriGiene, Health Care Antiseptic, 222 mL per bottle recall: Microbial Contamination of Non-Sterile Drug Product: The products were found
Microbial Contamination of Non-Sterile Drug Product: The products were found to be contaminated with the bacteria Burkholderia cepecia.
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Class II · 1+ years ago
Semaglutide, 2.5 mg/mL injection, 0.8 mL, Boothwyn Pharmacy recall: Subpotent Drug
Subpotent Drug
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NHTSA safety recall · 1+ years ago
Rivian Automotive R1S and R1T recall: 18.30. The Hands-Free Highway Assist (HWA) software may fail to correctly
18.30. The Hands-Free Highway Assist (HWA) software may fail to correctly identify a lead vehicle.
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NHTSA safety recall · 1+ years ago
Honda 2020-2022 and CRF1100 Africa Twin recall: The left handlebar switch harness may corrode due to oxidation
The left handlebar switch harness may corrode due to oxidation, resulting in the loss of horn function or the ability to switch the headlight from…