Montana Recalls

Orthofix U.S. LLC recalls Orthofix MINIRAIL, SHORT, LENGTHENER REF: M103, Unilateral

Unilateral external fixation devices may be incorrectly labeled. Minirail M101 was labeled as M103, Minirail M103 was labeled as M101, and Minirail M122 was labeled as M111

View recall details →

Orthofix U.S. LLC recalls Orthofix MINIRAIL, ARTICULATED, FIXATOR, VERTICAL AXIS REF:

Unilateral external fixation devices may be incorrectly labeled. Minirail M101 was labeled as M103, Minirail M103 was labeled as M101, and Minirail M122 was labeled as M111

View recall details →

Orthofix U.S. LLC recalls Orthofix ARTICULATED MINIRAIL FIXATOR HORIZONTAL AXIS REF:

Unilateral external fixation devices may be incorrectly labeled. Minirail M101 was labeled as M103, Minirail M103 was labeled as M101, and Minirail M122 was labeled as M111

View recall details →

Orthofix U.S. LLC recalls Orthofix MINIRAIL, STANDARD LENGTHENER Model/Catalog Number

Unilateral external fixation devices may be incorrectly labeled. Minirail M101 was labeled as M103, Minirail M103 was labeled as M101, and Minirail M122 was labeled as M111

View recall details →

Nutricia North America recalls functional formularies NOURISH ORGANIC WHOLE FOODS MEAL REPL

Subpotent for Vitamin A. The firm discovered that the testing laboratory used the wrong method when testing for Vitamin A. The test results gave a higher concentration of vitamin A than what is actually in the product.

View recall details →

Nutricia North America recalls functional formularies LIQUID HOPE ORGANIC WHOLE FOODS MEAL

Subpotent for Vitamin A. The firm discovered that the testing laboratory used the wrong method when testing for Vitamin A. The test results gave a higher concentration of vitamin A than what is actually in the product.

View recall details →

Encore Medical, LP recalls Brand Name: EMPOWR 3D KNEE Product Name: EMPOWR 3D KNEE INS,

Due to packaging discrepancy with incorrect product size mixed up.

View recall details →

Encore Medical, LP recalls Brand Name: EMPOWR 3D KNEE Product Name: EMPOWR 3D KNEE INS,

Due to packaging discrepancy with incorrect product size mixed up.

View recall details →

Beta Bionics, Inc. recalls iLet Bionic Pancreas, REF: BB1001

The reason for the recall is: it was found in version 3.3.6 of the iLet ACE Pump firmware and all previous releases that a screen unlock failure could occur when the user successfully slides the unlock slider on the Lock Screen, no screen transition occurs, and the user remains on the Lock Screen. Because the user cannot exit the Lock Screen, the user is unable to perform a cartridge change or meal announcement. If this occurs and therapy is in progress, therapy will continue normally until the insulin cartridge is depleted. The user will be unable to perform a cartridge change or a meal announcement and will be stuck on the screen until the battery fully drains. This can lead to hyperglycemia.

View recall details →

AMD Medicom Inc. recalls Ritmed Neurological Sponges, 0.75x0.75in, Sterile, REF: 8599

Neurological sponges used to moisten or absorb biological fluid during neurological surgery and may also be used to protect the brain during incision, may not consistently meet endotoxin specification for devices that contact the cerebrospinal fluid. Elevated endotoxin levels may lead to neurovascular adverse events, febrile response, and/or local transient inflammation, hypotension, or nausea.

View recall details →

AMD Medicom Inc. recalls Ritmed Neurological Sponges, Description/REF: 0.5x0.5in, N

Neurological sponges used to moisten or absorb biological fluid during neurological surgery and may also be used to protect the brain during incision, may not consistently meet endotoxin specification for devices that contact the cerebrospinal fluid. Elevated endotoxin levels may lead to neurovascular adverse events, febrile response, and/or local transient inflammation, hypotension, or nausea.

View recall details →

U.S. Tov, Inc. dba U.S. Trading Company recalls DRAGONFLY Thai Ginger Powder Net Weight: 4.37 oz (125 g) PRO

Potential contamination with lead.

View recall details →

Intuitive Surgical, Inc. recalls Brand Name: Da Vinci 5 Product Name: ASSY,DV5 TOWER,IS5000

Due to unintentionally activated near infrared handheld camera when attempting to turn off illumination during normal clinical workflow transitions, particularly when switching from the handheld camera to the robotic endoscope.

View recall details →

C.R. Bard Inc recalls Silastic Foley Catheters Silastic Brand Foley Catheter 30cc

Due to stain present on the surface of affected foley catheters.

View recall details →