Recalls affecting Guam
Notices that name Guam in their distribution area, plus every nationwide recall — nationwide recalls reach Guam too.
-
Class II · 7 months ago
I.T.S. GmbH I.T.S. Straight Plate with Angular Stability with the below recall: Updated MRI safety testing demonstrates higher RF-induced temperature
Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the…
-
Class I · 7 months ago
Erbe USA Inc Flexible Cryoprobe REF: 20402-411. For surgical use recall: Probes may rupture/burst during activation
Probes may rupture/burst during activation
-
Class I · 7 months ago
Merit Medical Systems, Inc. CentrosFLO Hemodialysis Catheters, REF: Cenfp15K/A recall: 16F dual-valved splittable sheath introducer due to a design defect
16F dual-valved splittable sheath introducer due to a design defect, may not split as intended, which may result in hemorrhage, foreign bodies…
-
Class II · 7 months ago
I.T.S. GmbH Distal Humeral Plates with Angular Stability with the below recall: Updated MRI safety testing demonstrates higher RF-induced temperature
Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the…
-
Class II · 7 months ago
I.T.S. GmbH HLS - Hand Locking Plates System with the below descriptions recall: Updated MRI safety testing demonstrates higher RF-induced temperature
Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the…
-
Class II · 7 months ago
Brand Name: Olympus PKS Cutting Forceps, 5mm 33cm Product Name: PKS recall: Olympus identified that the Cutting Forceps contain components
Olympus identified that the Cutting Forceps contain components for which the supplier did not adequately validate the welding process. Defective…
-
Class II · 7 months ago
I.T.S. GmbH I.T.S. Screw System with the below descriptions and corresponding recall: Updated MRI safety testing demonstrates higher RF-induced temperature
Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the…
-
Class III · 7 months ago
Philips S5-2 Ultrasound Transducer recall: To provide clarification and labelling to define the useful life
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
-
Class II · 7 months ago
I.T.S. GmbH Olecranonplate with Angular Stability with the below descriptions recall: Updated MRI safety testing demonstrates higher RF-induced temperature
Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the…
-
Class I · 7 months ago
Erbe USA Inc Flexible Cryoprobe w/ oversheath REF: 20402-401 Sterile EO recall: Probes may rupture/burst during activation
Probes may rupture/burst during activation
-
Class II · 7 months ago
I.T.S. GmbH FLS - Foot Locking Plates System and HOL - Hallux Osteotomy Locking recall: Updated MRI safety testing demonstrates higher RF-induced temperature
Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the…
-
Class I · 7 months ago
Philips Respironics Trilogy EV300, Software Version 1.05.15.00 recall: Using non-pneumatic nebulizers with Trilogy Evo Platform ventilators
Using non-pneumatic nebulizers with Trilogy Evo Platform ventilators may result in a discrepancy between the set tidal volume and the tidal volume…
-
Class I · 7 months ago
Philips Respironics Trilogy Evo Universal recall: Using non-pneumatic nebulizers with Trilogy Evo Platform ventilators
Using non-pneumatic nebulizers with Trilogy Evo Platform ventilators may result in a discrepancy between the set tidal volume and the tidal volume…
-
Class II · 7 months ago
I.T.S. GmbH HCS - Headless Compression Screw System, Headless Compression Screw recall: Updated MRI safety testing demonstrates higher RF-induced temperature
Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the…
-
Class II · 7 months ago
Orthalign, Inc Drill Plate, Ortho Dev. Trimax - Pegged, PREF Size 6-7 REF:402567 recall: Drill plates manufactured out of specification can result in a bone cut
Drill plates manufactured out of specification can result in a bone cut in excess 00800"(2.8448mm)
-
Class II · 7 months ago
Orthalign, Inc Drill Plate, Ortho Dev. Trimax - Pegged, PREF Size 1 -5 REF:402566 recall: Drill plates manufactured out of specification can result in a bone cut
Drill plates manufactured out of specification can result in a bone cut in excess 00800"(2.8448mm)
-
Class II · 7 months ago
Chiesi USA, Inc. Curosurf , 240 mg, Intratracheal Suspension, 3L Single-dose-Vial recall: Lack of Assurance of Sterility
Lack of Assurance of Sterility
-
Class III · 7 months ago
Radnostix Gelatin Capsule Pack for use with the Sodium Iodide I-131 Kit recall: Failed Tablet/Capsule Specifications
Failed Tablet/Capsule Specifications
-
Class II · 7 months ago
Amerisource Health Services LLC Meclizine Hydrochloride Tablets, USP 12.5 mg recall: Failed tablet specifications
Failed tablet specifications.
-
Class II · 7 months ago
Teva Pharmaceuticals USA, Inc Octreotide Acetate for Injectable Suspension recall: Lack of Assurance of Sterility: Quality system deficiencies identified during
Lack of Assurance of Sterility: Quality system deficiencies identified during a routine U.S Food and Drug Administration (FDA) inspection at the…
-
Class II · 7 months ago
Teva Pharmaceuticals USA, Inc Octreotide Acetate for Injectable Suspension recall: Lack of Assurance of Sterility: Quality system deficiencies identified during
Lack of Assurance of Sterility: Quality system deficiencies identified during a routine U.S Food and Drug Administration (FDA) inspection at the…
-
Class II · 7 months ago
Macleods Pharma USA, Inc Levothyroxine Sodium Tablets USP 150 mcg, 1000 Tablets bottle recall: Subpotent Drug
Subpotent Drug
-
Class II · 7 months ago
Teva Pharmaceuticals USA, Inc Octreotide Acetate for Injectable Suspension recall: Lack of Assurance of Sterility: Quality system deficiencies identified during
Lack of Assurance of Sterility: Quality system deficiencies identified during a routine U.S Food and Drug Administration (FDA) inspection at the…
-
Class I · 7 months ago
Nuts.com Inc. Nuts.com, Espresso Malted Milk Balls, 1 lb. sealed pouch & 20 lb. clear recall: Undeclared Allergen - Wheat and Soy (from Soy Lecithin). The ingredient
Undeclared Allergen - Wheat and Soy (from Soy Lecithin). The ingredient statement and allergen information do not include wheat or soy.