Recalls affecting Guam
Notices that name Guam in their distribution area, plus every nationwide recall — nationwide recalls reach Guam too.
-
Class II · 3 months ago
Pride Mobility Products Corp. Brand Name: Quantum Rehab Product Name: Q6 Edge 3 recall: If the "Remind Me Later" option is selected for user reminders
If the "Remind Me Later" option is selected for user reminders, reminder pop-up messages may appear while the wheelchair is in use. If this occurs…
-
Class II · 3 months ago
United Orthopedic Corp. Brand Name: U2 Total Knee System Product Name: PSA Box Trial recall: Due to an incomplete process of the component screw by a subcontractor
Due to an incomplete process of the component screw by a subcontractor which prevents the properly assembling of stem trail.
-
Class II · 3 months ago
Boston Scientific Corporation Radial Jaw 4 Jumbo Biopsy Forceps with the following recall: Potential for breach in sterile barrier of device packaging
Potential for breach in sterile barrier of device packaging.
-
Class I · 3 months ago
AVID Medical, Inc. Halyard convenience kits containing recalled Medline Namic recall: Affected kits contain Medline Namic Angiographic Star Off Handle Manifolds
Affected kits contain Medline Namic Angiographic Star Off Handle Manifolds, which were recalled by the manufacturer due to presence of particulates…
-
Class II · 3 months ago
United Orthopedic Corp. Brand Name: U2 Total Knee System Product Name: Femoral offset recall: Due to a design issue causing the incorrect engraved numbering on implant
Due to a design issue causing the incorrect engraved numbering on implant that could result in the incorrect orientation of the implant.
-
Class II · 3 months ago
Freudenberg Medical, LLC Blom-Singer Classic Indwelling Voice Prosthesis recall: Incorrect labeling- The labeled box for the Large Esophageal Flange contains
Incorrect labeling- The labeled box for the Large Esophageal Flange contains a Large Esophageal and Tracheal Flange, and the labeled box for the…
-
Class II · 3 months ago
Freudenberg Medical, LLC Blom-Singer Classic Indwelling Voice Prosthesis recall: Incorrect labeling- The labeled box for the Large Esophageal Flange contains
Incorrect labeling- The labeled box for the Large Esophageal Flange contains a Large Esophageal and Tracheal Flange, and the labeled box for the…
-
Class II · 3 months ago
Beckman Coulter Inc. REF # D23354, MicroScan LabPro V5.03 Panel Update 11 DVD Kit recall: Analyzers contain incorrect algorithms which may affect antimicrobial
Analyzers contain incorrect algorithms which may affect antimicrobial susceptibility test results, leading to false susceptibility classifications."
-
Class II · 3 months ago
GE Medical Systems Information Technologies Inc GE Healthcare MAC VU360, REF# recall: Software issue issue with the MAC VU360 v3.0 system. After selecting
Software issue issue with the MAC VU360 v3.0 system. After selecting the order refresh icon, an open preview or review screen might fail to close…
-
Class II · 3 months ago
Integrated Medcraft LLC Forward Oral Airway Kit . REF Number: 1011-40002. Containing recall: Devices could potentially contain an occluded or partially occluded Guedel
Devices could potentially contain an occluded or partially occluded Guedel Airway tip.
-
Class II · 3 months ago
Brand Name: OXOS Medical, Inc Product Name: MC2 Portable X-Ray System recall: Due to a defective circuit board that overheats
Due to a defective circuit board that overheats
-
Class II · 3 months ago
Siemens Healthcare Diagnostics, Inc. Atellica CH Urine Albumin REF: 11537225 recall: Processing of urine albumin assay on the CI analyzers may lead
Processing of urine albumin assay on the CI analyzers may lead to the following issues: Falsely depressed Atellica CH Urea Nitrogen (UN_c) results…
-
Class II · 3 months ago
United Orthopedic Corp. Brand Name: U2 Total Knee System Product Name: Femoral valgus recall: Due to an incomplete process of the component screw by a subcontractor
Due to an incomplete process of the component screw by a subcontractor which prevents the properly assembling of stem trail.
-
Class III · 3 months ago
Siemens Healthcare Diagnostics, Inc. Syva Emit tox Serum Tricyclic Antidepressant recall: out-of-specification sodium azide concentration in Syva Emit Tox Serum
out-of-specification sodium azide concentration in Syva Emit Tox Serum Tricyclic Antidepressant Calibrator/Controls Lot U2. While the assay results…
-
Class I · 3 months ago
Sunny Pharmtech Inc. Cyclophosphamide for Injection, USP, 1 gram/vial recall: Presence of Particulate Matter; identified as stainless steel
Presence of Particulate Matter; identified as stainless steel
-
Class II · 3 months ago
Zydus Pharmaceuticals Inc Mirabegron Extended-Release Tablets, 25 mg, 30-count bottle recall: CGMP: Due to Out of Specification (OOS) result for N-Nitroso Mirabegron
CGMP: Due to Out of Specification (OOS) result for N-Nitroso Mirabegron impurity.
-
Class I · 3 months ago
Sunny Pharmtech Inc. Cyclophosphamide for Injection, USP, 2 gram/vial recall: Presence of Particulate Matter; identified as stainless steel
Presence of Particulate Matter; identified as stainless steel
-
Class II · 3 months ago
Aurobindo Pharma USA Inc Dicyclomine Hydrochloride Capsules, USP, 10mg, 1,000 bottles recall: shortfill; reports of empty capsules
shortfill; reports of empty capsules.
-
Class I · 3 months ago
Akkarco LLC Ashfiat Alharamain Energy Support 250ml/8fl. oz recall: Undeclared tadalafil
Undeclared tadalafil
-
High - Class I · 3 months ago
City Foods, Inc. Ready-To-Eat Pastrami and Corned Beef products recall: Product Contamination
Product Contamination
-
Public Health Alert · 3 months ago
FSIS Issues Public Health Alert for Various Meat and Poultry Products Containing FDA-Regulated Jalapeños That Have Been Recalled Due To Possible…
Product Contamination
-
NHTSA safety recall · 3 months ago
Volvo Trucks VNL and VNR recall: The center roof marker lights may fail to illuminate
The center roof marker lights may fail to illuminate. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety…
-
NHTSA safety recall · 3 months ago
Toyota Tacoma Hybrid and Tacoma recall: The metal flange on the front and rear shock absorbers may corrode and fail
The metal flange on the front and rear shock absorbers may corrode and fail, resulting in detachment of the external oil reservoir.
-
NHTSA safety recall · 3 months ago
Toyota Camry Hybrid recall: The instrument cluster display may fail during vehicle startup
The instrument cluster display may fail during vehicle startup, deactivating the hazard lights, turn signals, seat belt warning system, and smart key…