Recalls affecting Guam
Notices that name Guam in their distribution area, plus every nationwide recall — nationwide recalls reach Guam too.
-
Class II · 10 months ago
Meridian Bioscience Inc Revogene C. difficile, in vitro diagnostic assay intended recall: The affected lots show a decline in performance over time
The affected lots show a decline in performance over time, which may lead to false-negative results.
-
Class II · 10 months ago
IMRIS Imaging Inc Brand Name: HFD100 Product Name: Head Fixation Device HFD100 Model/ recall: Torque screw may crack or separate. If used
Torque screw may crack or separate. If used, an affected screw could lead to inadequate head stabilization, compromised surgical precision…
-
Class I · 10 months ago
AVID Medical, Inc. Halyard Organ Recovery OR Pack, Kit Code: Llog1000-15 recall: Devices are not suitable for organ transplant
Devices are not suitable for organ transplant.
-
Class I · 10 months ago
AVID Medical, Inc. Halyard Organ Recovery OR Pack, Kit Code: Llof1000-17 recall: Devices are not suitable for organ transplant
Devices are not suitable for organ transplant.
-
Class II · 10 months ago
Beckman Coulter UniCel Dxl 800, Part numbers: 973100, A71456 recall: Beckman Coulter has determined that, due to a potential communication issue
Beckman Coulter has determined that, due to a potential communication issue, the analyzers listed above may not successfully restart following a…
-
Class II · 10 months ago
Beckman Coulter UniCel Dxl 600, Part numbers: A71460, A71461, A30260 recall: Beckman Coulter has determined that, due to a potential communication issue
Beckman Coulter has determined that, due to a potential communication issue, the analyzers listed above may not successfully restart following a…
-
Class II · 10 months ago
Medline Hudson RCI Medium Concentration Oxygen Masks: 1041CE recall: Firm received multiple complaints regarding tubing disconnecting from oxygen
Firm received multiple complaints regarding tubing disconnecting from oxygen mask. If issue occurs during use, may lead to delay in patient care and…
-
Class II · 10 months ago
Sophysa The Pressio 2 ICP Monitoring System recall: Customer complaints of Pressio monitor rebooting
Customer complaints of Pressio monitor rebooting.
-
Class II · 10 months ago
CareFusion 303, Inc. BD Pyxis ES Enterprise Server Catalog Numbers 1115-00 recall: Due a software issue that may result in equipment not receiving timely
Due a software issue that may result in equipment not receiving timely updates of patient, medication, or related information from enterprise systems.
-
Class II · 10 months ago
Integra LifeSciences Corp. Codman Microsensor Basic Kit recall: Potential corrosion stains on the surface of the 14-gauge Tuohy Needle
Potential corrosion stains on the surface of the 14-gauge Tuohy Needle that is included in the Microsensor and Cerelink ICP Kits.
-
Class II · 10 months ago
Imprimis NJOF, LLC Dexamethasone Moxifloxacin, 1 mg/mL and 5 mg/mL recall: Presence of particulate matter - Glass like particles
Presence of particulate matter - Glass like particles.
-
Class II · 10 months ago
Imprimis NJOF, LLC Dexamethasone Moxifloxacin Ketorolac, 1 mg/mL, 0.5 mg/mL recall: Presence of particulate matter - Glass like particles
Presence of particulate matter - Glass like particles.
-
Class III · 10 months ago
Alembic Pharmaceuticals Limited Fesoterodine Fumarate, Extended-release Tablets recall: Failed Impurities/Degradation Specifications: Due to levels of 'Diester
Failed Impurities/Degradation Specifications: Due to levels of 'Diester Impurity' exceeding the specification limit.
-
Class II · 10 months ago
AvKARE Rosuvastatin Tablets, USP, 10 mg recall: Out of specification for dissolution
Out of specification for dissolution.
-
Class II · 10 months ago
SpecGx, LLC Oxycodone and Acetaminophen CII Tablets USP, 7.5 mg/325 mg, 100 tablets recall: Failed Tablet/Capsule Specification: There is a potential for the imprint
Failed Tablet/Capsule Specification: There is a potential for the imprint to be missing on tablets.
-
Class II · 10 months ago
Tri-Moxi+¿ Single-Use Intraocular Injection, Imprimis NJOF, LLC recall: Presence of particulate matter - Glass like particles
Presence of particulate matter - Glass like particles.
-
Class II · 10 months ago
SpecGx, LLC Oxycodone and Acetaminophen CII Tablets USP, 10mg/325 mg, 100 tablets recall: Failed Tablet/Capsule Specification: There is a potential for the imprint
Failed Tablet/Capsule Specification: There is a potential for the imprint to be missing on tablets.
-
Class II · 10 months ago
Ziyad Brothers Importing Baraka Gourmet Pastry Kunafe 6.7oz recall: May contain partially hydrogenated oils
May contain partially hydrogenated oils
-
Class II · 10 months ago
MAYEJ COMERCIALIZADORA S. de R.L. de C.V. Italian Parsley packaged in 24lb boxes recall: pathogen Cyclospora cayetanensis
pathogen Cyclospora cayetanensis
-
Class II · 10 months ago
Ziyad Brothers Importing Baraka French Style Puff Pastry 1lb and 1.5lbs sizes recall: May contain partially hydrogenated oils
May contain partially hydrogenated oils
-
Highest risk · 10 months ago
Spring & Mulberry Mint Leaf Date Sweetened Chocolate Bar recall: Potential Foodborne Illness - Salmonella
Potential Foodborne Illness - Salmonella
-
Class II · 10 months ago
True Sea Moss Sea Moss Gel Superfood in various flavors recall: Potential Foodborne Illness - Botulism
Potential Foodborne Illness - Botulism
-
Class I · 10 months ago
Modern Warrior Dietary supplement capsules marketed for metabolism moosting recall: Unapproved new drug found to contain undeclared 1,4-DMAA and aniracetam
Unapproved new drug found to contain undeclared 1,4-DMAA and aniracetam, and tianeptine
-
Elevated risk · 10 months ago
HerbsForever Gastro Care capsule and Hingwastika powder and capsule dietary recall: Potential or Undeclared Allergen – Wheat
Potential or Undeclared Allergen – Wheat