Archive
502 recalls were announced in July 2018.
Of the 502 recalls this month scored against our rubric, 7% are Critical, 38% are Severe.
Which agencies issued them
Rock Run Industries is recalling LP Bottle Ring Brackets that may break, potentially causing propane cylinders to fall from vehicles.
Avella of Deer Valley, Inc. is recalling 40 bags of Heparin 1,000 Units in NS 250mL due to potential leakage that compromises sterility.
Zeiss is recalling 8 UV disinfection units for the Celldiscoverer 7 microscope because a firmware issue may allow the unit to activate outside its housing, exposing users to harmful UV radiation.
Cardinal Health is recalling Hydroline Trumpet Valves because the suction valve may not close properly, potentially causing continuous suction.
Tandem Diabetes Care is recalling 55 t:slim G4 Insulin Pumps because the fuel gauge may provide inaccurate battery readings, causing the pump to stop delivering insulin.
The Coca-Cola Company is recalling Odwalla Superfood fruit smoothies due to the potential for tiny wire metal fragments in the bottles.
Cardinal Health is recalling Hydroline Trumpet Valves because the suction valve may not close properly, potentially causing continuous suction.
Medtronic is recalling Tri-Staple 2.0 Black Intelligent Reloads because a missing sled component may prevent staple formation, potentially causing bleeding or leakage.
Cardinal Health 200, LLC is recalling Hydroline Trumpet Valves because the suction valve may not close properly, potentially causing continuous suction.
Cardinal Health is recalling Hydroline Trumpet Valves because the suction valve may not close properly, potentially causing continuous suction.
Cardinal Health 200, LLC is recalling Hydroline Trumpet Valves because the suction valve may not close properly, potentially causing continuous suction.
AesDex is recalling 587 Cardica C-Port xA PLUS Anastomosis Systems because the handle mechanism may break during use, causing a loud noise and potential dispersion of plastic fragments.
Ethicon is recalling 588 units of Proline Suture Blue 4x18" 5/0 due to a packaging design issue that may allow the needle to perforate the package, posing a risk of injury or infection.
Avella of Deer Valley is recalling 480 single-dose hydromorphone syringes due to potential bag leakage and lack of sterility assurance.
Cardinal Health 200, LLC is recalling Hydroline Trumpet Valves because the suction valve may not close properly, potentially causing continuous suction.
Ethicon is recalling specific Proline sutures because a packaging design issue allows the needle to perforate the package, posing a risk of injury or infection.
Ethicon is recalling specific Proline sutures because the needle may perforate the packaging, posing a risk of soft tissue injury or infection.
NewDeal SA is recalling Large QWIX medical devices because their use may cause superficial or deep infections requiring antibiotic treatment or device removal.
Ethicon, Inc. is recalling 432 units of Prolene Suture 30" 8-0 Blue (D8292) because the needle may perforate the packaging, posing a risk of injury or infection.
Cardinal Health 200, LLC is recalling Hydroline Trumpet Valves because the suction valve may not close properly, potentially causing continuous suction.
Ethicon, Inc. is recalling specific Prolene suture products because a packaging design issue allows the needle to perforate the package, posing a risk of injury or infection.
Cardinal Health is recalling Hydroline Trumpet Valves because the suction valve may not close properly, potentially causing continuous suction.
Ethicon, Inc. is recalling specific Prolene suture products because a packaging design issue allows the needle to perforate the package, posing a risk of injury or infection.
Ethicon is recalling specific Prolene suture products because a packaging design issue allows needles to perforate the package, posing a risk of injury or infection.
Ethicon is recalling specific PRONOVA suture needles because a packaging design issue may allow the needle to perforate the package, posing injury or infection risks.
Avella of Deer Valley is recalling specific lots of ePHEDrine 50mg syringes because bags may leak, compromising sterility.
Ethicon is recalling specific Proline sutures because a packaging design issue allows needles to perforate the package, posing injury and infection risks.
Ethicon is recalling specific Prolene suture products because a packaging design issue may allow needles to perforate the package, posing injury and infection risks.
Ethicon is recalling specific Proline suture products because the needle may perforate the packaging, posing a risk of soft tissue injury or infection.
Hitachi Medical Systems America Inc is recalling 264 Oasis MRI systems because an exposed stainless steel belt can cause finger cuts.
Avella of Deer Valley, Inc. is recalling 15 cassettes of fentanyl and bupivacaine due to potential bag leakage and lack of sterility assurance.
GE Medical Systems is recalling T2100 Microflex Drive Treadmills because unaddressed spare parts may cause uncontrolled walking belt motion during stress tests.
Ethicon is recalling 372 units of Proline Suture Blue 18" 7-0 because the needle may perforate the packaging, posing a risk of soft tissue injury or infection.
Ethicon is recalling specific Prolene suture products because a packaging design issue allows needles to perforate the package, posing risks of soft tissue injury or infection.
Ethicon is recalling specific Prolene suture units because a packaging design issue allows needles to perforate the package, posing injury and infection risks.
Wescam Inc is recalling 29 MX-10 surveillance laser systems because the ocular hazard distance is longer than specified, posing a risk of eye exposure.
Ethicon is recalling specific Proline suture products because a packaging design issue allows needles to perforate the package, posing injury and infection risks.
Siemens is recalling 197 units of Dimension Vista MULTI 1 SDIL diluent due to a potential defect in the vial cap septum that may cause inaccurate test results.
NewDeal SA is recalling TIBIAXYS devices because use may cause superficial or deep infections requiring antibiotic treatment or device removal.
T R Toppers, Inc. is recalling Chopped Chocolate Pretzel Pieces due to potential peanut contamination. Consumers should check for Lot 10481 and stop using the product.
Ethicon is recalling 300 units of Proline Suture 30" 6-0 Blue because a packaging design issue may allow the needle to perforate the package, posing injury or infection risks.
Opgen Inc is recalling AdvanDx QuickFISH Slides because they may show diminished performance before their expiration date.
Edwards Lifesciences is recalling one SAPIEN 3 Transcatheter Heart Valve because it was packaged with the incorrect valve size relative to the label.
Cardinal Health is recalling 8,928 Presource PBDS kits because a defect in the Gatorade pouch seal caused the pouch to leak within the kit.
The Hain Celestial Group is recalling alba BOTANICA sport mineral sunscreen because the wrong product formulation was placed in the packages.
Philips is recalling 32 Ingenuity Digital PET/CT Systems because a block connecting the patient pallet to the couch may be assembled incorrectly, potentially causing a misaligned screw.
Cardinal Health is recalling Presource PBDS kits because a defect in the Gatorade pouch seal caused the pouch to leak within the kit.
Stryker is recalling 180 reprocessed Harmonic Ace shears because they may display an error code preventing use.
Siemens Healthcare Diagnostics is recalling 1,446 units of Dimension Vista CTNI Sample Diluent because a defective cap septum may cause erroneously elevated test results.
Medtronic is voluntarily recalling Vectris Trial Screening Lead Kits because a manufacturing defect in the curved tip introducer needle may cause difficulty advancing or withdrawing the lead.
Valeris Medical is recalling 113 Apollo XT Suture Anchors because the labels incorrectly identified the material as titanium instead of PEEK.
Fx Solutions is recalling specific proton beam therapy heads due to a breach in the external blister packaging.
Cardinal Health is recalling 8,928 Presource PBDS kits because a defect in the Gatorade pouch seal caused the pouch to leak within the kit.
Sun Pharmaceutical Industries is recalling one lot of Metformin Hydrochloride Extended Release Tablets because a piece of rubber glove was detected in a tablet.
Fx Solutions is recalling specific lots of Humelock Offset Heads due to a breach in the external blister packaging.
Intel-GE Care Innovations LLC is recalling the Health Harmony Mobile application because patient data sometimes failed to sync with the backend database in a timely manner.
Canadian Hospital Specialties is recalling specific lots of pediatric feeding tubes because they may be packaged with the incorrect length as labeled.
Siemens is recalling 1,195 units of Dimension Vista MULTI 2 SDIL diluent because a defective septum may cause erroneously elevated test results.
Cardinal Health is recalling 8,928 Presource PBDS kits because a defect in the Gatorade pouch seal caused the pouch to leak within the kit.
SynTec is recalling S3B 45-inch Restraint School Bus Seats because the mounting foot may pull through the bolted joint at the bus floor, increasing injury risk in a crash.
JCPenney is recalling Okie Dokie Denim Patches Shortie shorts because the patches can detach, posing a choking hazard to young children.
Ross Stores is recalling Bronze Hammered bistro chairs because the frames can break, posing a fall hazard. Consumers should stop using the chairs and return them for a full refund.
Karma Automotive is recalling 2018 Revero vehicles because the driver's side exterior rearview mirror may use convex glass instead of flat glass, failing federal safety standards.
Meritor is recalling specific wheel studs installed in steer axle hubs because improper heat treatment may cause them to fail, potentially leading to wheel detachment.
Jost International is recalling certain Outboard Sliders because a narrow bracket may allow the trailer to separate from the tractor, increasing crash risk.
Braun Corporation is recalling 2012-2018 BraunAbility Dodge and Chrysler wheelchair vans because brake lines may be disconnected, reducing electronic stability control performance.
Daimler Trucks is recalling 2018-2019 Freightliner Business Class M2 trucks because an incorrectly installed steering shaft may disconnect the steering wheel from the front wheels.
Van-Con is recalling 2011-2018 33803 Dual Rear Wheel school buses because seat foam may not absorb enough impact in a crash, increasing injury risk.
The USDA FSIS issued a public health alert for Hungry Man frozen dinners containing whey powder recalled due to possible Salmonella contamination. No adverse reactions have been reported.
Daimler Trucks is recalling 2017-2019 Freightliner Cascadia trucks because the instrument cluster may fail to check ABS and ESC warning lights, increasing crash risk.
Ducati is recalling 2018 Panigale and Hypermotard motorcycles because rear brake pad friction material may detach, increasing stopping distance and crash risk.
Polaris is recalling 2011-2016 GEM electric vehicles because a cracked lower frame tube can cause the upper cab frame to fail, increasing injury risk.
Polaris is recalling 2016-2017 GEM E2, E4, E6, and ELXD vehicles because a faulty drive mode switch may cause the vehicle to move in the opposite direction intended.
Thor Motor Coach is recalling 2018-2019 Outlaw motorhomes because they lack required rear reflex reflectors, which reduces visibility to other drivers.
Yamaha is recalling 3,493 2018 MT-07 and XSR700 motorcycles because drive chain guard bolts may loosen, causing the guard to break and fall onto the road.
Peanut Processors, Inc. is recalling 30 lb boxes of Dry Roasted Peanut Meal after a customer reported the product tested positive for Salmonella.
Gaia Ethnobotanical LLC is recalling specific lots of Gaia Kratom powder due to FDA-confirmed Salmonella contamination.
Gaia Ethnobotanical LLC is recalling Gaia Kratom powder due to FDA-confirmed Salmonella contamination. Consumers should stop using the product.
Nectar Foods LLC is recalling Honey Mama's Oregon Peppermint Cacao-Nectar Bars due to undeclared almonds, a major food allergen.
Gaia Ethnobotanical LLC is recalling Gaia Kratom powder due to FDA analysis confirming Salmonella contamination.
Gaia Ethnobotanical LLC is recalling Gaia Kratom powder due to FDA-confirmed Salmonella contamination.
Gaia Ethnobotanical LLC is recalling Gaia Kratom powder due to FDA analysis confirming salmonella contamination.
Win Opportunity Knocks is recalling approximately 6,020 pounds of fresh and frozen raw ground beef products due to possible contamination with Shiga toxin-producing E. coli.
Gaia Ethnobotanical LLC is recalling various Gaia Kratom powder products nationwide due to FDA-confirmed Salmonella contamination.
Gaia Ethnobotanical LLC is recalling Gaia Kratom powder due to FDA-confirmed Salmonella contamination.
Gaia Ethnobotanical LLC is recalling specific lots of Gaia Kratom powder due to FDA-confirmed Salmonella contamination.
Gaia Ethnobotanical LLC is recalling Gaia Kratom powder due to FDA-confirmed Salmonella contamination.
Gaia Ethnobotanical LLC is recalling Green Dragon Kratom powder due to FDA-confirmed Salmonella contamination.
Gaia Ethnobotanical LLC is recalling Green Malay Kratom powder due to FDA-confirmed Salmonella contamination.
Gaia Ethnobotanical LLC is recalling Gaia Kratom powder due to FDA-confirmed Salmonella contamination. Consumers should stop using the product.
Gaia Ethnobotanical LLC is recalling Gaia Kratom powder due to FDA analysis confirming Salmonella contamination.
Gaia Ethnobotanical LLC is recalling Gaia Kratom powder due to FDA-confirmed Salmonella contamination.
Gaia Ethnobotanical LLC is recalling Red Dragon Kratom powder due to Salmonella contamination found by FDA analysis.
Gaia Ethnobotanical LLC is recalling Gaia Kratom powder due to FDA-confirmed Salmonella contamination. Consumers should stop using the product.
Gaia Ethnobotanical LLC is recalling Gaia Kratom powder due to FDA-confirmed Salmonella contamination.
Gaia Ethnobotanical LLC is recalling Gaia Kratom powder due to FDA-confirmed Salmonella contamination.
Gaia Ethnobotanical LLC is recalling Gaia Kratom powder due to FDA-confirmed Salmonella contamination.
Gaia Ethnobotanical LLC is recalling Gaia Kratom powder due to FDA-confirmed Salmonella contamination.
Peanut Processors, Inc. is recalling dry roasted peanut granules after a customer reported the product tested positive for Salmonella.
Brew Dr. Kombucha is recalling Clear Mind kombucha bottles because glass fragments were found inside. Consumers should stop using the affected products.
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