Archive
758 recalls were announced in June 2017.
Of the 758 recalls this month scored against our rubric, 4% are Critical, 19% are Severe.
Which agencies issued them
Ethicon Endo-Surgery Inc is recalling 792 units of the Endopath ETS-FLEX Endoscopic Articulating Linear Cutter due to a risk of pinion gear failure under extreme use cases.
Roche Diagnostics is recalling 1,603 units of Elecsys PreciControl Varia 3 because the e-barcode and value sheet contain a typographical error for PTH target values.
Zimmer Biomet is voluntarily recalling 16 units of the Modular Hybrid Glenoid Base Large after two pieces with quality defects were shipped.
Arrow International is recalling VPS Access Kits because they lack required information regarding the included 3M Tegaderm CHG dressing.
Trident Seafoods is recalling Panko Breaded Alaska Cod because it may contain small pieces of plastic.
Medtest Holdings is recalling Pointe Scientific Lactate Dehydrogenase Reagent Sets because the product's stability claim is not being met.
Trident Seafoods is recalling frozen Alaska Cod Diamond Cut Squares because they may contain small pieces of plastic.
Toshiba is recalling 70 Angio WorkStation units because the Peak Skin Dose value may display incorrectly if the workstation is powered on after the Infinix system.
Trident Seafoods is recalling frozen Alaska Cod Rectangles because they may contain small pieces of plastic.
Forest Laboratories is recalling Saphris (asenapine) sublingual tablets because blister packs labeled as 10 mg actually contain 5 mg tablets.
AbbVie is recalling 3,331 PEG kits distributed in the US and 31 other countries because they may have missing components, duplicate parts, or missing labels.
Trident Seafoods is recalling frozen breaded cod products because they may contain small pieces of plastic. The recall affects 7 cases distributed across 26 states.
Exact Sciences is recalling 15 Sample Mixer 2 units in Wisconsin due to door damage incidents caused by the Sample Holder lid.
VistaPharm is recalling Nystatin Oral Suspension because it contains an impurity peak that exceeds approved specifications.
Trident Seafoods is recalling frozen Alaska Cod Rectangles because they may contain small pieces of plastic. The product was distributed in 26 states.
AbbVie is recalling specific lots of PEG Kits due to potential defects including missing components, duplicate parts, or missing labels and instructions.
Acumed LLC is voluntarily removing the Slide-Loc Anatomic Radial Head System from the market due to complaints about instrumentation performance, trial design, and implant dissociations.
Invacare is recalling 5,020 Assist Bed Rail 6632 units because a typo in the user manual could lead to incorrect installation.
Siemens is recalling certain lots of SHBG Immulite 2000 reagents because they may not meet stability claims, potentially causing test bias.
Cell Marque is recalling CD117, c-kit reagents because they were not labeled 'For Export Only' as required by the FD&C Act.
Tosoh Bioscience is recalling 64 boxes of AIA-PACK TgAb Control Set because the labels included instructions for a non-FDA approved methodology.
Cell Marque is recalling Her2/Neu (c-erbB-2) reagents because they were not labeled as 'For Export Only' as required by law.
Tosoh Bioscience is recalling 15 boxes of AIA-PACK TPOAb Control Sets because the labels included instructions for a non-FDA approved methodology.
Acumedia is recalling 10 units of Sabouraud Dextrose Agar in Illinois due to incorrect storage temperature information on the label.
Cell Marque is recalling Adenovirus reagents because they were not properly labeled as 'For Export Only' as required by the FD&C Act.
Acumedia Manufacturers recalled 5 units of Nutrient Gelatin because the label displayed an incorrect expiration date.
Cell Marque is recalling specific lots of Estrogen Receptor reagents because they were not labeled 'For Export Only' as required by law.
Cell Marque is recalling specific lots of Herpes Simplex Virus II reagents because they were not properly labeled as 'For Export Only' as required by federal law.
Cell Marque is recalling Herpes Simplex Virus I reagents because they were not properly labeled as 'For Export Only' as required by the FD&C Act.
Cell Marque is recalling three units of SV40 (MRQ-4) reagent because they were not labeled 'For Export Only' as required by law.
Sandoz Inc is recalling 4,464 bottles of Amoxicillin and Clavulanate Potassium tablets found to be subpotent in clavulanic acid.
Cell Marque is recalling 8 units of Estrogen Receptor reagent because they were not properly labeled as 'For Export Only' as required by the FD&C Act.
Randox Laboratories is recalling 198 kits of Liquid Urine Control Level 3 due to a labeling error affecting Total Protein values.
Cell Marque is recalling Varicella Zoster Virus reagents because they were not properly labeled as 'For Export Only' as required by the FD&C Act.
Cell Marque is recalling Her2/Neu (EP3) reagents because they were not properly labeled as 'For Export Only' as required by the FD&C Act.
Cell Marque is recalling HHV-8 in vitro diagnostic reagents because they were not properly labeled as 'For Export Only' as required by the FD&C Act.
Acumedia Manufacturers, Inc. is recalling 16 units of Beef Extract Powder (PN 7228) because the label displays an incorrect expiration date.
Cell Marque is recalling five units of H. pylori reagent because they were not properly labeled as 'For Export Only' as required by the FD&C Act.
Arctic Cat is recalling about 2,700 snowmobiles because the drive clutch can fracture, causing fragments to escape the shielding and posing an impact hazard.
Lila + Hayes is recalling about 600 units of Eloise and Benton Bubble children's playwear because buttons can detach, posing a choking hazard to young children.
Hyundai is recalling 2017 Santa Fe Sport vehicles because the driver's seat belt anchor bolt may not be sufficiently tightened, increasing injury risk in a collision.
Forest River is recalling 2016-2017 XLR ToyHauler trailers because axle equalizers are too long, which may cause failure and loss of vehicle control.
Vactor is recalling 2015-2017 Jetter vehicles because an unexpected idle rise may overpower the parking brake, increasing crash risk.
Daimler Vans USA is recalling 2016 Mercedes-Benz Sprinter 2500 and 3500 vehicles because the B-pillar tire labels list incorrect, low tire pressures.
Creation Gardens is recalling approximately 22,832 pounds of raw ground beef and primal cuts shipped to food service locations in four states due to possible E. coli O157:H7 contamination.
Hyundai is recalling 2013-2017 Santa Fe and Santa Fe Sport vehicles because the secondary hood latch cable may corrode, potentially allowing the hood to open while driving.
Hyundai is recalling 2015-2016 Sonata and Genesis vehicles because the parking brake indicator light may fail to illuminate due to switch corrosion.
Motor Coach Industries is recalling 2014-2017 J4500 motor coaches because over-tightened front brake hose clamps may damage the hoses, potentially increasing stopping distance and crash risk.
P&S Bakery is recalling approximately 2,959 pounds of Gia Russa brand pepperoni rolls due to possible contamination with clear meat casing. No illnesses have been reported.
Eldorado Mobility is recalling 2010-2017 Amerivan 10 vehicles because rear suspension air bags may fail unexpectedly, increasing the risk of a crash.
Thor Motor Coach is recalling 2017 Challenger 37YT motorhomes because the generator exhaust pipe may be mislocated or missing, creating a carbon monoxide risk.
Correctional Industries Airway Heights is recalling approximately 319,000 pounds of frozen meat and poultry products because they were produced using water with unsafe chemical levels.
McNeilus is recalling 2016-2017 Bridgemaster V concrete mixers because the backup alarm and camera may shut off during extended reversing, increasing injury risk.
Mazda is recalling 2004-2008 RX-8 vehicles because heat may crack the fuel pump pipe, causing a fuel leak and increasing fire risk.
Mazda is recalling 2004 RX-8 vehicles because a crack in the front suspension lower control arm ball joint socket may cause the ball joint to separate, potentially leading to loss of steering control.
Polaris is recalling 2015-2017 Slingshot vehicles because missing grommets on replacement swingarms may allow debris to contaminate the rear wheel speed sensor, disabling ABS and traction control.
Toyota is recalling 2016-2017 Tacoma vehicles with six-cylinder engines because a faulty crank position sensor may cause the engine to stall, increasing crash risk.
Kreative Kids is recalling about 7,600 children's robes because they fail to meet federal flammability standards for sleepwear, posing a risk of burn injuries.
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