Archive
771 recalls were announced in May 2017.
Of the 771 recalls this month scored against our rubric, 6% are Critical, 23% are Severe.
Which agencies issued them
The Anspach Effort, Inc. is recalling 31 Large Craniotome, Black Max units because the supplied directions for use did not include a recommended service interval.
The Anspach Effort, Inc. is recalling 216 units of the 11.25cm Black Max attachment because the supplied directions for use did not include a recommended service interval.
The Anspach Effort, Inc. is recalling 618 Minimal Access Attachment pneumatic systems because the supplied directions for use did not contain a recommended service interval.
Smith & Nephew is recalling 1,416 units of Renovation Radial Osteotome Blades because stability data does not support the labeled 10-year shelf life.
The Anspach Effort, Inc. is recalling 121 Bearing Sleeves because the supplied directions for use did not contain a recommended service interval.
The Anspach Effort, Inc. is recalling 22 Sagittal Saw pneumatic systems because the supplied directions for use did not contain a recommended service interval.
The Anspach Effort, Inc. is recalling 177 units of the 16cm Minimally Invasive Attachment because the supplied directions for use did not contain a recommended service interval.
The Anspach Effort, Inc. is recalling 19 AL-III pneumatic systems because the supplied directions for use did not contain a recommended service interval.
The Anspach Effort, Inc. is recalling three Pediatric Craniotomes because the supplied directions for use did not contain a recommended service interval.
The Anspach Effort, Inc. is recalling 182 Bearing Sleeve, 10CM Curved units because the supplied directions for use did not contain a recommended service interval.
The Anspach Effort, Inc. is recalling five AL-III-DISS Adapters because the supplied directions for use did not contain a recommended service interval.
The Anspach Effort, Inc. is recalling three IMRI Motor pneumatic systems because the supplied directions for use did not contain a recommended service interval.
The Anspach Effort, Inc. is recalling 293 eMax2 Hybrid Hand Controls because the supplied directions for use did not contain a recommended service interval.
The Anspach Effort, Inc. is recalling 375 units of 7.5cm QD Angle Attachments because the supplied directions for use did not contain a recommended service interval.
The Anspach Effort, Inc. is recalling 7.5cm Angle Attachments because the supplied directions for use did not contain a recommended service interval.
The Anspach Effort, Inc. is recalling two Black Max contra angle attachments because the supplied directions for use did not contain a recommended service interval.
The Anspach Effort, Inc. is recalling 10 IMRI CRANI-A pneumatic attachments because the supplied directions for use did not include a recommended service interval.
The Anspach Effort, Inc. is recalling 821 Electronic Foot Controls because the supplied directions for use did not contain a recommended service interval.
Fagron, Inc. is recalling Zinc Oxide Paste 25% because of an incorrect strength value in the Drug Facts Panel.
The Anspach Effort, Inc. is recalling 10 units of the 90 Degree Right Angle Attach, Black Max, because the supplied directions for use did not contain a recommended service interval.
Zimmer Trabecular Metal Technology, Inc. is recalling the TM Ardis Interbody System due to a procedural error in the approval of literature, resulting in the unauthorized release of certain content.
The Anspach Effort, Inc. is recalling 13 units of the 10.5cm Angle Attachment, Black Max, because the supplied directions for use did not include a recommended service interval.
The Anspach Effort, Inc. is recalling 25 BLACKMAX-NEURO LOW PRESSURE pneumatic systems because the supplied directions for use did not include a recommended service interval.
The Anspach Effort, Inc. is recalling 16 Autolube-III pneumatic systems because the supplied directions for use did not contain a recommended service interval.
The Anspach Effort, Inc. is recalling 13.5CM Angle Attachments because the supplied directions for use did not contain a recommended service interval.
The Anspach Effort, Inc. is recalling 49 Rotating Adult Craniotomes because the supplied directions for use did not contain a recommended service interval.
The Harvard Drug Group is recalling Aripiprazole Tablets, 2 mg, due to out-of-specification assay results. The recall covers 36,990 tablets distributed nationwide and in Puerto Rico.
The Anspach Effort, Inc. is recalling 5,757 units of the 5.0cm Short Attachment because the supplied directions for use did not contain a recommended service interval.
The Anspach Effort, Inc. is recalling 16 Small Attachment, J-Latch units because the supplied directions for use did not contain a recommended service interval.
The Anspach Effort, Inc. is recalling 6.8cm Controlled Depth Attachments because the supplied directions for use did not contain a recommended service interval.
The Anspach Effort, Inc. is recalling 462 System Console units because the supplied directions for use did not contain a recommended service interval.
Chrysler is recalling 2017 Jeep Compass vehicles because the left front halfshaft may not be properly seated, potentially causing loss of drive or vehicle roll.
Profile Design is recalling Cobra S bicycle handlebar stems because they can corrode and break, causing riders to lose control and crash.
Mercedes-Benz is recalling 5,818 vehicles because electronic stability control software may keep brakes slightly applied, increasing crash and fire risks.
FCA US LLC is recalling 2013-2016 Ram 1500, 2500, and 3500 trucks because a sensor fault may disable side curtain air bags and seat belt pretensioners, increasing injury risk in crashes.
Norgren Inc. is recalling one Kneeling Module because improperly seated snap rings may cause a loss of suspension air pressure, increasing crash and injury risks.
The USDA FSIS issued a public health alert for frozen ready-to-eat fried chicken and pork sausage products due to possible Listeria monocytogenes contamination. No illnesses have been reported.
Polaris is recalling about 6,000 model year 2017 RMK and SKS snowmobiles because a steering post weld can separate, causing loss of control.
American Honda is recalling about 2,200 2017 Pioneer 700 recreational off-highway vehicles because a manufacturing defect may cause the front passenger seat belt buckle to fail.
General Motors is recalling 2016-2017 Chevrolet Spark vehicles because the front passenger air bag may injure an unbelted child's neck during deployment.
Ford Brothers Wholesale Meats is recalling beef patties because they contain soy, a known allergen, that is not declared on the label.
Forest River is recalling 2017 XLR ToyHauler trailers because the Federal Placard incorrectly lists rear tire pressure as 50psi instead of 80psi, which could lead to tire failure.
Perdue Foods is recalling 2,148 pounds of Italian Style Organic Chicken Sausage due to possible blue plastic contamination. No injuries have been reported.
TRW is recalling aftermarket lower ball joints for Toyota 4Runner, Sequoia, and Tundra vehicles because a design defect could cause steering loss and increase crash risk.
Segway is recalling specific off-board chargers for Personal Transporters because a wire can detach and cause a shock hazard. No injuries have been reported.
DGFA is recalling about 200 women's scarves sold on Amazon because they fail to meet federal flammability standards, posing a burn risk.
Springs Window Fashions is recalling motorized window coverings sold with Zeus brand lithium batteries due to fire and burn hazards.
Akron Brass Company is recalling Ultrajet firefighting nozzles because internal components may bind, limiting water output and hindering firefighting efforts.
KZRV is recalling 2018 Sport Trek and Durango travel trailers with outside kitchens due to potential propane line leaks that could cause fire or explosion.
Marcho Farms is recalling approximately 5,620 pounds of veal, beef, and pork products due to possible non-O157 Shiga toxin-producing E. coli contamination.
Honda is recalling 2015-2016 CR-Vs that received replacement engines potentially built with wrong pistons, which may cause engine stalls and increase crash risk.
Combi USA is recalling about 1,000 Shuttle Travel Systems because the car seat can disengage from the stroller frame, posing a fall hazard to infants.
Jim Reed's Truck Sales is recalling 2014-2016 Hino 338 trucks because certification labels fail to identify the final stage manufacturer, potentially hindering safety recall awareness.
Deutsch Kase Haus is recalling cheddar cheese products due to potential Listeria monocytogenes contamination. Affected brands include Guggisberg, Amish Classics, Dutch Farms, and Banquet.
Deutsch Kase Haus, LLC is recalling Pepper-Jack cheese due to potential Listeria monocytogenes contamination. The product was sold under multiple private labels in 11 states.
Deutsch Kase Haus, LLC is recalling approximately 4.1 million pounds of Colby cheese due to potential Listeria monocytogenes contamination. The product was distributed in 11 states.
Deutsch Kase Haus, LLC is recalling bulk cream due to potential Listeria monocytogenes contamination. The product was distributed to multiple states.
Valley Bakery Wholesalers Inc is recalling Large Hamburger Buns because they contain egg but do not declare it on the label.
Deutsch Kase Haus, LLC is recalling White Colby cheese due to potential Listeria monocytogenes contamination. The product was distributed in 11 states.
Guggisberg Cheese Inc is recalling specific lots of Marble Cheese because the product may contain Listeria monocytogenes.
Deutsch Kase Haus is recalling private-label farmers cheese due to potential Listeria monocytogenes contamination. Affected products were distributed in 11 states.
Valley Bakery Wholesalers Inc is recalling Wheat Tea Rolls because the product contains egg but does not declare it on the label.
Guggisberg Cheese Inc is recalling specific lots of Monterey Jack Cheese because the product may contain Listeria monocytogenes.
Deutsch Kase Haus, LLC is recalling Amish Creamery cheese products due to potential Listeria monocytogenes contamination. The recall affects multiple private-label brands distributed across eleven states.
Henry-Broch Co is recalling 15,268 cartons of Jalapeno Powder due to potential Salmonella contamination. The product was distributed in New Jersey and Texas.
Deutsch Kase Haus, LLC is recalling approximately 4.1 million pounds of Colby-Jack cheese due to potential Listeria monocytogenes contamination. The product was distributed to 11 states.
Deutsch Kase Haus, LLC is recalling specific cheese by-products due to potential Listeria monocytogenes contamination. The products were distributed across eleven states.
Deutsch Kase Haus is recalling Colby-Jack cheese products due to potential Listeria monocytogenes contamination. The recall affects private-label brands sold in 11 states.
Guggisberg Cheese Inc is recalling specific lots of Farmers Cheese because the product may contain Listeria monocytogenes.
Deutsch Kase Haus, LLC is recalling bulk liquid whey due to potential Listeria monocytogenes contamination. The product was distributed to multiple states.
Deutsch Kase Haus, LLC is recalling specific lots of semi-soft cheese due to potential Listeria monocytogenes contamination. The affected products were distributed to multiple states.
Valley Bakery Wholesalers Inc is recalling Large Hamburger Buns because they contain egg but do not declare it on the label.
Armada Nutrition is recalling MusclePharm Assault pre-workout powder because a raw material initially failed testing for Staphylococcus aureus, raising concerns about potential contamination.
Guggisberg Cheese Inc is recalling Garden Vegetable Natural Cheese because it may contain Listeria monocytogenes. The product was distributed to 13 states.
Isomeric Pharmacy Solution, LLC is recalling 4,001 vials of Methylprednisolone Acetate and Lidocaine HCl injection due to production processes that cannot assure sterility.
Isomeric Pharmacy Solution, LLC is recalling 2,352 vials of Methylprednisolone Acetate and Lidocaine HCl injection due to production processes that cannot assure sterility.
Bevovations, LLC is recalling specific apple cider products due to elevated levels of patulin. The recall covers 1,409 cases distributed in New Hampshire, Connecticut, Massachusetts, and Rhode Island.
Arrow International is recalling 310 units of Arrowg+ard Blue Plus Central Venous Catheterization Kits due to possible voids in the catheter hub that could lead to interlumen crossover.
Guggisberg Cheese Inc is recalling Colby Cheese sold under multiple brands due to potential Listeria monocytogenes contamination.
Valley Bakery Wholesalers Inc is recalling Specialty Crimp products because they contain egg but do not declare it on the label.
Valley Bakery Wholesalers Inc is recalling Blueberry Tea Rings because the product contains egg but does not declare it on the label.
Guggisberg Cheese Inc is recalling Amish Creamery Butter Cheese because it may contain Listeria monocytogenes. The product was distributed to 13 states.
Valley Bakery Wholesalers Inc is recalling 7 packages of Steak Buns because they contain egg but do not declare it on the label.
Valley Bakery Wholesalers Inc is recalling 13 packages of Brat Buns because they contain egg but do not declare it on the label.
Guggisberg Cheese Inc is recalling specific lots of Pepper Jack Cheese because the product may contain Listeria monocytogenes.
Whole Foods Market is recalling 6-pack Banana Choc Chip Muffins sold in Massachusetts due to undeclared walnuts.
Valley Bakery Wholesalers Inc is recalling Raisin Bread because it contains egg but does not declare it on the label.
Valley Bakery Wholesalers Inc is recalling 14 packages of Large Wheat Hamburger Buns because they contain egg but do not declare it on the label.
Guggisberg Cheese Inc. is recalling specific lots of cheddar cheese because the product may contain Listeria monocytogenes.
Guggisberg Cheese Inc is recalling Thunder Jack Cheese sold as Amish Classic Firecracker due to potential Listeria monocytogenes contamination.
Volkswagen Group of America is recalling 2017 Audi Q5 vehicles because a gearbox defect may allow the vehicle to roll unexpectedly while in Park.
Volkswagen Group of America is recalling 2013-2017 Audi Q5 and Q7 vehicles because a fuel pump flange may crack, allowing fuel to leak and increasing fire risk.
Valley Bakery Wholesalers Inc is recalling 91 packages of hamburger buns because they contain egg but do not declare it on the label.
TP Food Processing Inc. is recalling Shrimp Satay and Lemongrass Satay sauces because improper production makes them susceptible to Clostridium botulinum contamination.
Valley Bakery Wholesalers Inc is recalling 21 packages of hot dog buns because they contain egg but do not declare it on the label.
Isomeric Pharmacy Solution, LLC is recalling 2,156 vials of Testosterone Cypionate and Propionate injection due to production processes that cannot assure sterility.
Isomeric Pharmacy Solution, LLC is recalling 2,335 vials of Triamcinolone Acetonide and Lidocaine HCl injection due to production processes that cannot assure sterility.
TP Food Processing is recalling Lemongrass Satay and Shrimp Satay because the acidified sauces were not properly produced, making them susceptible to Clostridium botulinum contamination.
Savaria Concord Lifts is recalling 74 Omega Incline Platform Lifts because loose bolts can cause the carriage to separate from the trolley, leading to unit failure.
Sigma Foods is recalling specific lots of Menu Del Sol Beans and Cheese Burritos due to potential Listeria monocytogenes contamination.
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