Archive
446 recalls were announced in October 2022.
Of the 446 recalls this month scored against our rubric, 2% are Critical, 21% are Severe.
Which agencies issued them
Hobbs Medical, Inc. is recalling Hobbs Helical Retrieval Baskets with lot numbers ending in R due to incorrect expiration dates on device labels. Affected units were distributed worldwide from March 2018 to September 2020.
Novis PR, LLC recalled G-PREPROTEIN Liquid Dietary Supplement due to atypical bottle appearance, unusual odor, and atypical bubbles when opened. The recall affects 1,369 units distributed in Puerto Rico.
Hobbs Medical Spray Catheter devices sold between March 2018 and September 2020 have incorrect expiration dates on their labels. The error may extend the device's shelf life beyond its actual expiration.
Hobbs Medical is recalling Helical Retrieval Baskets with incorrect expiration dates on labels. The labeled shelf life extends beyond the actual safe duration for device use.
Hobbs Medical is recalling Biliary Pigtail Stent Kits with incorrect expiration dates on labels. The incorrect dates extend the product shelf life, potentially allowing devices to be used past their actual expiration.
Hobbs Medical is recalling Cytology Brush Catalog Number 4206 due to incorrect expiration dates on product labels that extend the intended shelf life. Approximately 300 units were distributed nationwide and internationally between March 2018 and September 2020.
Hobbs Medical is recalling Freeman Pancreatic Flexi-Stent devices with incorrect expiration dates on labels. Affected units distributed in the US and internationally from 2018 to 2020 may have extended shelf lives beyond accuracy.
Hobbs Medical is recalling Hobbs Posi-Stop Injection Needles due to incorrect expiration dates on device labels that extend the shelf life. Affected devices have lot numbers ending in 'R' distributed from 2018–2020.
Hobbs Medical is recalling Helical Retrieval Baskets due to incorrect expiration dates on device labels. The mislabeling extends the shelf life, potentially allowing use of expired devices.
Hobbs Medical is recalling polypectomy snares with incorrect expiration dates on labels. Affected devices have lot numbers ending in R and were distributed from March 2018 to September 2020.
Hobbs Medical is recalling Freeman Pancreatic Flexi-Stent devices distributed between March 2018 and September 2020 due to incorrect expiration dates on product labels. The mislabeled devices display extended shelf-life information that does not reflect actual product safety.
Baxter Healthcare recalls Prismaflex HF Set devices due to a mistranslation in Estonian language instructions. The mistranslation contains contradictory information about patient body weight restrictions.
PACCAR is recalling 2023 Kenworth and Peterbilt trucks because improperly heat-treated tie rod clamps may fail, causing a sudden loss of steering.
Harley-Davidson is recalling certain 2019-2022 Touring, Trike, and CVO models due to a software error causing brake lights to illuminate without rider input. This malfunction may confuse other drivers and increase crash risk.
Comoto is recalling specific Bilt Grommet Youth helmets that may not adequately protect the wearer during a crash.
Spartan Fire is recalling 2021-2023 emergency vehicles because improperly heat-treated tie rod clamps may fail, causing loss of steering.
Precision Industries is recalling two 2021 Spartan Fire Metrostar emergency vehicles because an electrical defect can cause vehicle lighting to fail.
PACCAR is recalling certain 2022-2023 Kenworth and Peterbilt trucks whose digital displays may freeze. A frozen display prevents critical safety information like vehicle speed and warning lights from appearing.
AdvancePierre Foods is recalling approximately 4,137 pounds of frozen pork loin steak fritters that may contain hard pieces of plastic. No illnesses have been reported.
SAF-Holland is recalling certain ULX40 suspensions because a retaining clip may detach, potentially reducing brake performance or causing a flat tire.
Shyft Group is recalling 2023 Spartan K4 motorhomes because an incorrectly installed parking brake valve may cause the brake to engage unexpectedly, increasing crash risk.
HD Trailer is recalling 2022 Non-CDL Gooseneck trailers because improper axle spindle welds may crack or separate, increasing crash risk.
Starcraft is recalling 2021-2022 Autumn Ridge Outfitter travel trailers because the cooktop flame may invert when the stove and furnace operate simultaneously, increasing the risk of fire or injury.
Jayco is recalling 2021-2022 Jay Feather, Jay Flight, and Jay Flight SLX travel trailers because the cooktop flame may invert when the stove and furnace operate simultaneously, increasing fire and injury risks.
Highland Ridge RV is recalling 2021-2022 travel trailers because the cooktop flame may invert when the stove and furnace operate simultaneously, increasing fire and injury risks.
U-Line is recalling about 90 Outdoor Series 24-inch built-in convertible freezers that can overheat and pose a fire hazard. U-Line has received three reports of freezer fires with no injuries reported.
BRP is recalling certain 2022 Ski-Doo snowmobiles with 850 E-TEC engines due to a loose fuel injector hose retainer screw that can cause fuel leaks and fires. The company has received five fuel-leak reports, resulting in two fires.
General Motors is recalling 2022-2023 Hummer EV Pickups and 2022 BrightDrop EV600s because the high-voltage battery pack may not be sealed, allowing water entry that can cause loss of drive power.
About 22,000 Ancheer e-bikes with lithium-ion batteries are being recalled because the batteries can ignite, explode, or spark, causing fire and burn injuries. Consumers should stop using the recalled bikes immediately and contact Ancheer for a free replacement battery and mount.
Addo Play has recalled about 9,300 Early Learning Centre Little Senses Lights & Sounds Shape Sorter Toys sold on Amazon from October 2020 through August 2022. The red cube can detach during use and release a small white ball, posing a choking hazard to infants.
U.P. Fashion is recalling approximately 1,800 children's rings sold nationwide at dollar stores and discount stores from April 2021 through July 2022 because the metal base contains lead levels exceeding the federal lead content ban.
Chrysler is recalling the 2022-2023 Jeep Wrangler PHEV for battery fuse defects caused by incorrect fasteners. The fuses can overheat and fail, causing loss of drive power and increasing the risk of a crash.
USDA issued a public health alert for specific Frank's Butcher Shop ground beef packages due to possible E. coli O103 contamination found in routine testing.
Storyteller Overland is recalling 2022-2023 Mode LT motorhomes because improperly routed wiring may contact the axle, causing damage and increasing fire risk.
Cressi-Sub USA is recalling about 1,350 scuba buoyancy compensator devices (BCDs) with defective inflator hoses that may fail to inflate properly, posing a drowning hazard to divers.
Jammers Apparel Group is recalling about 450 children's nightgowns sold at JCPenney from March to May 2022 because they fail to meet federal flammability standards and pose a burn risk to children.
Ekouaer children's bathrobes fail to meet federal flammability standards for sleepwear, posing a burn risk to children. About 9,200 units sold on Amazon between March 2020 and July 2021 are affected.
Nissan is recalling certain 2022 Titan XD and related models because the in-vehicle infotainment system may continuously reboot when restarted, causing the rearview display to become inoperative and reducing rear visibility.
Chrysler is recalling specific Mopar 3.0L Diesel Engines because the high-pressure fuel pump may fail, causing the engine to stall and increasing crash risk.
Chrysler is recalling 2020-2022 Jeep Wranglers, Gladiators, and Ram 1500s due to potential fuel pump failure that may cause engine stall, increasing crash risk. Dealers will replace the pump at no cost.
Jayco is recalling 2023 Seismic and Seismic Luxury trailers because the fuel cap does not fit properly, which may cause fuel leaks and increase fire risk.
Certain 2022 RAM 1500 vehicles have front seat belt retractors with improperly welded components that may fail to restrain occupants during a crash. Chrysler is replacing the affected retractors free of charge.
Newair is recalling about 11,750 Magic Chef Air Fryers because they can overheat, posing fire and burn hazards. Consumers should stop using them immediately and contact Newair for a refund.
Renaissance Food Group is recalling 3 Skewer Veggie Kabobs due to confirmed Listeria monocytogenes contamination. Products were distributed in Alabama, Georgia, and South Carolina.
Renaissance Food Group is recalling its Small Ranch Tray with Dip due to positive test results for Listeria monocytogenes. Products were distributed to Alabama, Georgia, and South Carolina.
Renaissance Food Group is recalling Mushroom Stir Fry Blend after testing detected Listeria monocytogenes in the finished product. Products were distributed to Alabama, Georgia, and South Carolina.
Renaissance Food Group is recalling Large Mild Salsa (13 oz) due to positive Listeria monocytogenes test results. Products were distributed to Alabama, Georgia, and South Carolina.
Renaissance Food Group is recalling Mexican Style Layered Bean Dip (1.25 lb) distributed in Alabama, Georgia, and South Carolina due to positive test results for Listeria monocytogenes.
Arcade Industries candy corn sold at Shapiro Produce stores in Massachusetts and Connecticut is recalled due to undeclared egg allergen. People with egg allergies risk allergic reaction.
Philips Respironics is recalling the Therapy Mask 3100 NC/SP because the product lacks warnings about magnetic components that may affect patients with implantable devices or metallic splinters in the eyes.
Renaissance Food Group is recalling Diced Red Onion (10 oz units) distributed to Alabama, Georgia, and South Carolina due to positive test results for Listeria monocytogenes in finished product.
Daimler Trucks North America is recalling 2011-2023 Thomas Built EFX and HDX school buses because exterior roof panels may separate during a crash.
Renaissance Food Group is recalling Tri-Pepper Blend (7 oz units) due to positive test results for Listeria monocytogenes. All products manufactured with the same components are included in the recall.
Kenover Marketing Corp. is recalling Mighty Sesame Organic Tahini over potential Salmonella contamination. Approximately 13,766 units were distributed to stores across 20 states.
Renaissance Food Group is recalling 12 oz packages of Snacking Peppers due to positive test results for Listeria monocytogenes. All products manufactured with the same components are affected.
Renaissance Food Group is recalling diced bell pepper and white onion products due to positive test results for L. monocytogenes. The recalled products were distributed in Alabama, Georgia, and South Carolina.
Renaissance Food Group is recalling Hatch Chile Guacamole Blender due to positive test results for Listeria monocytogenes. Products were distributed to Alabama, Georgia, and South Carolina.
Renaissance Food Group is recalling Large Medium Salsa (13 oz) after positive test results for Listeria monocytogenes were detected in finished product. All products made with the same components are included in the recall.
Renaissance Food Group is recalling Medium Hatch Salsa (13 oz units) because positive test results detected Listeria monocytogenes in the finished product. The affected salsa was distributed to Alabama, Georgia, and South Carolina.
Renaissance Food Group is recalling Vegetable Bowl products because testing found Listeria monocytogenes contamination. The products were distributed to Alabama, Georgia, and South Carolina.
Renaissance Food Group is recalling Small Medium Hatch Chile Pico de Gallo (9 oz units) because positive tests detected Listeria monocytogenes in the finished product. All products made with the same components are included in the recall.
Renaissance Food Group is recalling 106 units of Seasoned Squash Onion & Dill due to detection of Listeria monocytogenes. Products were distributed to Alabama, Georgia, and South Carolina.
Antigua Farmacista Hand Sanitizer Ocean Citron (473 mL bottles) is being recalled because the product was found to contain benzene. The affected lot was distributed in Florida and Washington only.
Philips Respironics is recalling Wisp and Wisp Youth nasal masks because they lack warnings about magnetic components that could interfere with implanted medical devices or cause eye injuries from metallic splinters.
Philips Respironics is recalling 930,813 DreamWisp Nasal Masks worldwide due to missing warnings about magnetic components that could interfere with implantable medical devices or cause metallic splinters.
Philips Respironics Amara View Full-Face Mask lacks critical safety warnings about magnetic components for patients with implantable medical devices. The Class I recall affects 5.6 million units worldwide.
Philips Respironics is recalling DreamWear Full Face CPAP masks due to missing warnings about magnetic components that may pose risks to patients with implantable devices or metallic eye splinters.
Renaissance Food Group is recalling Fajita Mix due to positive test results for Listeria monocytogenes in the finished product. The recall affects products distributed in Alabama, Georgia, and South Carolina.
Renaissance Food Group is recalling Mango Habanero Blender (9 oz units) because positive test results detected Listeria monocytogenes in the finished product.
Renaissance Food Group is recalling Hamburger Fixin's (10 oz units) distributed in Alabama, Georgia, and South Carolina due to positive test results for Listeria monocytogenes in the finished product.
Renaissance Food Group is recalling Large Mild Chunky Guacamole (13 oz) due to positive test results for Listeria monocytogenes in the finished product.
Renaissance Food Group is recalling Asparagus Saute' products due to positive test results for Listeria monocytogenes. The recalled products were distributed to Alabama, Georgia, and South Carolina.
Renaissance Food Group is recalling Steak Topper seasoning (7.5 oz units) due to positive test results for Listeria monocytogenes. The affected product was distributed in Alabama, Georgia, and South Carolina.
Renaissance Food Group is recalling Fiesta Corn (10 oz) after positive test results confirmed Listeria monocytogenes in the finished product. All products made with the same components are affected.
Renaissance Food Group is recalling Mild Guacamole Blender products due to positive test results for Listeria monocytogenes. The affected products were distributed in Alabama, Georgia, and South Carolina.
Renaissance Food Group is recalling Spicy Guacamole Blender products because positive test results confirmed Listeria monocytogenes contamination in the finished product.
Fresenius Kabi is recalling the Ivenix Infusion System (IIS) LVP Software version 5.2.0 because the display screen may freeze and become unresponsive, stopping medication flow and requiring immediate clinician intervention.
Salon Technologies International is recalling Sanitizing Hand Spray 80% due to GMP deviations: the product contains acetaldehyde and acetal above specification limits. The recall affects 1,656 bottles distributed in Florida and Washington.
Cipla recalls Arformoterol Tartrate Inhalation Solution due to environmental monitoring failure affecting sterility assurance.
Synthes is recalling Hammertoe Continuous Compression Implant (CCI) Kits because the drill pin is incompatible with the included drill template, which may delay surgery or cause soft tissue damage and adverse tissue reactions.
Coca-Cola Southwest Beverages LLC is recalling Coca-Cola Classic 12 FL OZ metal cans in 12-pack fridge packs due to the presence of metal particles in the product.
Wright Medical Technology recalls 32 units of Stryker EVOLVE Proline Stem due to labeling mismatch: outer packages are labeled with one stem size but contain a different size. Surgeons should verify device size before implantation.
Hologic recalls 233 BioZorb LP Markers nationwide due to removable labels showing incorrect expiration dates. Implants labeled with January 2022 dates may be mistakenly used after their actual July 2024 expiration.
Wright Medical is recalling EVOLVE Proline Stem devices due to labeling errors where the outer package does not match the device inside. Affected devices are size-mismatched, which could lead to incorrect surgical placement.
B. Braun is recalling 94,000 Introcan Safety FEP 14G catheters due to potential leakage at the catheter hub. Affected units were distributed in the US and Canada.
Eden's Answers Inc is recalling Sprigs Lil Ones Sleepy Time herbal supplement due to high bacterial growth in the product. Consumers should stop using it immediately.
Zimmer, Inc. is recalling certain G7 Acetabular System acetabular shells (52 MM and 60 MM) because the outer sterile package has corner walls thinner than specification, which could crack during transit and potentially lead to surgical complications or infection.
Pfizer is recalling Aminophylline Injection vials due to a complaint of particulate matter (hair) in one vial. Over 103,000 vials were distributed to the US and Puerto Rico.
WFM 365 Organic Creamy Caesar dressing is recalled because the product does not declare wheat and soy allergens on its label. Consumers with wheat or soy allergies should not consume this product.
Blue Bird is recalling 2023 Vision and All-American transit buses because the entrance door handrail diameter is too small to meet ADA standards, posing a slip and fall risk.
IN MY BATHROOM LLC is recalling 485 units of the Seago SG-153 handheld UV-C germicidal wand nationwide due to excessive ultraviolet-C radiation. Consumers should stop using the device and contact the manufacturer for instructions.
Aurora Products is recalling its Aurora Natural brand Organic Cranberry Frontier Mix due to undeclared peanuts. People with peanut allergies are at risk.
2022 Volkswagen ID.4 vehicles have rearview cameras that may be delayed or deactivated, reducing rear visibility and increasing the risk of crashes. Dealers will provide a free software update.
Eden's Answers Inc is recalling Sprigs Dental Health, an herbal dietary supplement, due to detection of high bacterial growth. The product was distributed across 37 states.
Philips has recalled MR Patient Care Portal 5000 desktop units (Model 453564792561) due to intermittent audio failure. The device may fail to produce audio, and standard troubleshooting does not reliably resolve the issue.
Dr. Reddy's Laboratories is recalling Phytonadione Injectable Emulsion USP due to out-of-specification aluminum content results found during 12-month stability testing.
Eden's Answers Inc is recalling Sprigs Honey Herbal Syrup dietary supplement due to high bacterial growth within the product. The affected product was distributed across multiple states.
Woodbine Products is recalling FOAMFRESH DYE FREE ANTIBACTERIAL HAND WASH due to incorrect scent information on the label. The affected lots VDAF017 and VDAF018 were distributed in North Carolina, and no illnesses have been reported.
Fila Manila Coconut Jam (12 oz, UPC 860003619353) is being recalled because it contains undeclared gluten. Consumers with gluten sensitivity should not consume the product.
AuroMedics Pharma LLC is recalling one lot of Tranexamic Acid Injection due to the presence of metal particles found in a vial. The affected product was distributed nationwide.
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