Archive
771 recalls were announced in May 2017.
Of the 771 recalls this month scored against our rubric, 6% are Critical, 28% are Severe.
Which agencies issued them
The Anspach Effort, Inc. is recalling 14 IMRI Short Attachment units because the supplied directions for use did not include a recommended service interval.
Breg Inc is recalling 2,609 units of If Hip Sterile Polar Dressings because some may have unsealed pouches, rendering them non-sterile.
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 98 Minimal Access Straight Drivers because the supplied directions for use did not contain a recommended service interval.
The Anspach Effort, Inc. is recalling 203 units of the 10.5cm QD Angle Attachment because the supplied directions for use did not contain a recommended service interval.
The Anspach Effort, Inc. is recalling 2,339 units of the 5.0cm Heavy Duty Short Attachment because the supplied directions for use did not contain a recommended service interval.
Tradewind Foods is recalling Goya Octopus in Olive Oil because the product contains squid instead of octopus. This labeling error affects consumers in Puerto Rico and the Caribbean.
The Anspach Effort, Inc. is recalling 207 Electronic Foot Controls because the supplied directions for use did not contain a recommended service interval.
The Anspach Effort, Inc. is recalling 9,829 pneumatic attachments because the supplied directions for use did not include a recommended service interval.
Smith & Nephew is recalling Renovation Thin Osteotome Blades because stability data does not support the labeled 10-year shelf life.
The Anspach Effort, Inc. is recalling 293 eMax2 Hybrid Hand 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 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 7.5cm Angle Attachments 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 16 Small Attachment, J-Latch units 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 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 three IMRI Motor pneumatic systems because the supplied directions for use did not contain a recommended service interval.
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 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 10 units of the 90 Degree Right Angle Attach, Black Max, 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 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 821 Electronic Foot Controls because the supplied directions for use did not contain 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 6.8cm Controlled Depth 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 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 462 System Console units because the supplied directions for use did not contain a recommended service interval.
Profile Design is recalling Cobra S bicycle handlebar stems because they can corrode and break, causing riders to lose control and crash.
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.
Mercedes-Benz is recalling 5,818 vehicles because electronic stability control software may keep brakes slightly applied, increasing crash and fire risks.
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.
General Motors is recalling 2016-2017 Chevrolet Spark vehicles because the front passenger air bag may injure an unbelted child's neck during deployment.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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, 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 Amish Creamery cheese products due to potential Listeria monocytogenes contamination. The recall affects multiple private-label brands distributed across eleven states.
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 bulk liquid whey due to potential Listeria monocytogenes contamination. The product was distributed to multiple states.
Deutsch Kase Haus is recalling cheddar cheese products due to potential Listeria monocytogenes contamination. Affected brands include Guggisberg, Amish Classics, Dutch Farms, and Banquet.
Guggisberg Cheese Inc is recalling specific lots of Monterey Jack Cheese because the product may contain Listeria monocytogenes.
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 Farmers Cheese because the product may contain Listeria monocytogenes.
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, LLC is recalling bulk cream due to potential Listeria monocytogenes contamination. The product was distributed to multiple 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.
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.
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 specific lots of semi-soft cheese due to potential Listeria monocytogenes contamination. The affected products were distributed to multiple states.
Guggisberg Cheese Inc is recalling specific lots of Marble Cheese because the product may contain Listeria monocytogenes.
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.
Valley Bakery Wholesalers Inc is recalling 7 packages of Steak Buns because they contain egg but do not declare it on the label.
Armada Nutrition is recalling Performix Crea-Bead creatine supplements because a raw material initially failed testing for Staphylococcus aureus, raising concerns about potential contamination.
Valley Bakery Wholesalers Inc is recalling 47 packages of Tea Rolls because the product contains egg but does not declare it on the label.
Whole Foods Market is recalling 6-pack Banana Choc Chip Muffins sold in Massachusetts due to undeclared walnuts.
Armada Nutrition is recalling MusclePharm Assault pre-workout powder because a raw material initially failed testing for Staphylococcus aureus, raising concerns about potential contamination.
Isomeric Pharmacy Solution, LLC is recalling 5,165 bottles of Phenylephrine 2.5% and Tropicamide 1% ophthalmic drops due to a lack of assurance of sterility.
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 cheddar cheese because the product may contain Listeria monocytogenes.
Isomeric Pharmacy Solution, LLC is recalling 2,335 vials of Triamcinolone Acetonide and Lidocaine HCl injection due to production processes that cannot assure sterility.
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.
Valley Bakery Wholesalers Inc is recalling Wheat Hamburger Buns because they contain egg but do not declare it on the label.
Valley Bakery Wholesalers Inc is recalling Cherry Tea Rings because they contain egg but do not declare it on the label.
The FDA is recalling hCG Body Shaper because it was marketed without approval and contains human chorionic gonadotropin, making it an unapproved drug.
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.
Valley Bakery Wholesalers Inc is recalling 21 packages of hot dog buns because they contain egg but do not declare it on the label.
Valley Bakery Wholesalers Inc is recalling Specialty Crimp products because they contain egg but do not declare it on the label.
Medtronic is notifying clinicians that an improved splice kit is available to replace the HeartWare HVAD Pump Driveline Splice Kit due to a safety issue.
Sigma Foods is recalling specific lots of Menu Del Sol Beans and Cheese Burritos due to potential Listeria monocytogenes contamination.
Maple Leaf Foods is recalling approximately 24,768 pounds of frozen quiche products that entered the U.S. without required FSIS re-inspection.
Guggisberg Cheese Inc is recalling specific lots of Pepper Jack Cheese because the product may contain Listeria monocytogenes.
Valley Bakery Wholesalers Inc is recalling Large Hamburger Buns because they contain egg but do not declare it on the label.
Valley Bakery Wholesalers Inc is recalling 10 packages of Cocktail Buns because the product contains egg but does not declare it on the label.
Volkswagen Group of America is recalling 2017 Audi Q5 vehicles because a gearbox defect may allow the vehicle to roll unexpectedly while in Park.
Guggisberg Cheese Inc is recalling Thunder Jack Cheese sold as Amish Classic Firecracker due to potential Listeria monocytogenes contamination.
Valley Bakery Wholesalers Inc is recalling Apricot Tea Rings because the product contains egg but does not declare it on the label.
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.
Porsche is recalling 2015-2017 Macan models because a fuel pump flange may crack, causing a fuel leak that increases fire risk.
Valley Bakery Wholesalers Inc is recalling Almond Tea Rings because they contain egg but do not declare it on the label.
Valley Bakery Raisin Buns are being recalled because they contain egg but do not declare it on the label.
Looking for a different month? Back to 2017.