Archive
662 recalls were announced in March 2022.
Of the 662 recalls this month scored against our rubric, 4% are Critical, 25% are Severe.
Which agencies issued them
Bard Peripheral Vascular is recalling 49,760 SAFE-T PLUS lumbar puncture trays for adults due to manometer leaking and mating issues. Healthcare providers should discontinue use and contact the manufacturer.
Bard Peripheral Vascular Inc. recalls SAFE-T PLUS lumbar puncture trays due to manometer leaking and mating issues affecting device function. The FDA Class II recall covers 15,650 devices distributed nationwide and internationally.
Boston Scientific is recalling 32 units of DREAMTOME endoscopic devices due to a sterile barrier breach that compromises device sterility, creating potential infection risk. No illnesses have been reported.
Bard Peripheral Vascular Inc recalled 3,240 SAFE-T PLUS Adult lumbar puncture trays due to manometer failures involving leaking and defective mating connections.
Bard Peripheral Vascular Inc is recalling pediatric lumbar puncture trays due to manometer leaking and mating failures that could prevent proper pressure measurement during procedures.
Bio-Rad's BioPlex 2200 Syphilis Test Reagent Pack is being recalled due to concerns that COVID-19 vaccines may interfere with test results, and due to manufacturing defects affecting reagent stability.
Sam Medical Products is recalling 2,950 packages of SAM CHEST SEAL (Model CS203-EN, Lot Y060321-09) with defective dressing containing holes that prevent creating an occlusive seal for chest wounds.
Boston Scientific is recalling 254 units of the Hydratome RX 44-20MM medical device worldwide due to a compromised sterile barrier that may affect device sterility.
Family Pharmacy of Statesville is recalling Trimix injectable vials (Alprostadil/Papaverine/Phentolamine 20 mcg/30 mg/0.5 mg) due to lack of assurance of sterility. The recall affects 2 vials distributed in North Carolina.
Boston Scientific is recalling RX Cholangiogram Kits because the sterile barrier has been breached, compromising the sterility of the devices. The affected kits were distributed worldwide.
Herbalife International is recalling Herbalife NutritionProtein Bar Deluxe in Chocolate Peanut flavor nationwide due to undeclared egg allergen. The product poses a risk to consumers with egg allergies.
Stutzman Farms is recalling its Organic All Purpose Flour sold in bulk due to undeclared wheat allergen. The flour was distributed across seven states and may affect individuals with wheat allergies.
Stutzman Farms is recalling 4oz and 8oz bags of Sourdough Einkorn Pretzels due to undeclared wheat allergen. Consumers with wheat allergies should not consume this product.
Wright Medical Technology's ORTHOLOC Non-Locking Screw was recalled due to a packaging error in lot #73967511638696, where locking screws were mistakenly packaged instead. The affected product was distributed to France.
Fresh Creative Foods is recalling its Red Sauce Chicken Enchilada Kit due to plastic pieces discovered during manufacturing. The contamination came from ice supplied to the manufacturer.
Port City Soups Baton Rouge Beans in 32-oz glass jars are being recalled due to an unapproved production process for acidified foods. The recall affects products sold in Alabama, Louisiana, Mississippi, and Tennessee.
RMJV LP's First Street brand basil pesto sauce is recalled because hard plastic pieces were found in the product during manufacturing, traced to supplier ice.
Boston Scientific is recalling 96 units of JAGTOME RX medical devices due to a sterile barrier breach that compromises device sterility. Patients should contact their physician if they received this device.
Fresh Creative Foods is recalling Thai Noodle Salad due to hard clear plastic pieces found during manufacturing. The contamination originated from ice supplied to the manufacturer.
Port City Soups Creole Gumbo is being recalled because the production process was not approved for acidified foods. The product should not be consumed.
Boston Scientific is recalling 7,115 units of JAGTOME REVOLUTION RX devices worldwide due to sterile barrier breach that could allow contamination.
Vbest Inc is recalling salted dried plums (saladitos) distributed in California and Washington due to high lead levels detected by the California Department of Public Health. Consumers should not consume the affected product.
Boston Scientific has recalled 3,578 units of the JAGTOME RX medical device due to sterility compromise from a barrier breach. Affected units were distributed worldwide.
Walmart's Freshness Guaranteed Broccoli Cheddar Pasta Salad is recalled due to hard plastic pieces found during manufacturing. The contamination came from ice purchased from a supplier and affects products with use-by dates of March 14–22, 2022.
Boston Scientific is recalling 98 units of the JAGTOME RX 39-30-260-025 medical device due to compromised sterile barrier that affects device sterility. Units were distributed worldwide.
Candies Tolteca is recalling Tolteca Saladitos Salted Dried Plums due to potential high lead contamination. Consumers should not consume affected product.
Fresh Creative Foods is recalling Thai Peanut Dressing due to the presence of hard plastic pieces potentially found in the product. The plastic originated from ice used during manufacturing.
ConAgra Foods is recalling Rosarita Organic Refried Beans due to possible contamination with small rocks. The recall affects approximately 169,680 cases distributed across seven states.
Candies Tolteca is recalling Tolteca Saladitos dried plums with chili and lemon due to potential high lead levels. Approximately 1,248 bags were distributed in California, Utah, and Nevada.
Fresh Creative Foods is recalling Lemon Capellini Salad due to hard clear plastic pieces found in the product. The contamination source was traced to ice purchased from a supplier.
Swanson Health Products is recalling Swanson Ultra Vitamin B12 Methylcobalamin supplements due to potential metal shavings in the product. The contamination poses a choking and injury risk.
Arcimoto Inc. is recalling certain 2019-2022 motorcycles because the brake pressure switch may corrode when exposed to salt and de-icer chemicals. Corroded switches cause brake lights to illuminate constantly, confusing other drivers and increasing crash risk.
Boston Scientific is recalling 98 JAGTOME RX medical devices due to a sterile barrier breach. The affected units were distributed worldwide.
Boston Scientific is recalling 982 units of DREAMTOME medical devices due to sterile barrier breach that compromises device sterility. Affected units were distributed worldwide.
Stutzman Farms is recalling Organic All Purpose Einkorn Flour sold in bulk due to undeclared wheat allergen. The product was distributed across seven Midwest states.
Bentley Motors is recalling certain 2020-2022 Continental GT and Flying Spur vehicles due to incorrectly installed front seat belt assemblies that may lack an automatic locking retractor, potentially failing to secure child restraints properly in a crash.
PS Seasoning & Spices is recalling its Honey Sriracha Snack Stick Seasoning due to undeclared wheat. The product was distributed to multiple U.S. states and Canada.
Boston Scientific is recalling 4,487 JAGTOME RX medical devices worldwide due to sterility compromise from a sterile barrier breach. Users face contamination risk if devices are used.
Medtronic is recalling 8 LINQ II Insertable Cardiac Monitors due to moisture ingress susceptibility that may cause loss of functionality. Affected devices were distributed in the US (NJ, NY, PA, VA) and Italy.
Boston Scientific is recalling Hydratome RX 44-30MM/260CM devices due to a sterile barrier breach that could compromise device sterility. The recall affects 3,371 units distributed worldwide.
Alliance RV is recalling certain 2022 Valor, Paradigm, and Avenue travel trailers due to faulty power inlet bolts that can cause loose wiring and electrical fire risk. Dealers will replace the power inlet free of charge.
Fifteen Boston Scientific DREAMTOME medical devices are being recalled due to a sterile barrier breach that compromises device sterility. The affected lot number 27802363 requires appropriate action.
GE Healthcare is recalling 10,445 CARESCAPE Central Station monitoring systems. If connected to an unapproved keyboard, audio alarms may be muted, potentially preventing users from receiving critical notifications.
USDA FSIS issued a public health alert for specific Charlie's Produce salads containing undeclared allergens like peanut, wheat, egg, and milk. Consumers should not eat these products.
Bio-Rad Laboratories is recalling 724 BioPlex 2200 Syphilis Calibrator sets due to COVID-19 vaccine interference concerns and manufacturing problems with reagent stability. The recalled lots were distributed nationwide in the U.S. and internationally.
PS Seasoning & Spices, Inc. recalled Honey BBQ Snack Stick Seasoning containing undeclared wheat, affecting approximately 10,441 units distributed across multiple U.S. states and Canada. Consumers with wheat allergies should not consume affected products.
LivaNova is recalling four Sorin Centrifugal Pump CP5 Drive Units because a ferrite ring on the power cable may be missing. The units were distributed in Florida, Texas, and Nebraska.
CellEra LLC is recalling Vitale Silver calcium alginate wound dressings nationwide due to incorrect instructions for use containing language beyond FDA-cleared content.
The Harvard Drug Group is recalling hydrALAZINE HCl Tablets, USP, 10 mg due to failed impurity and degradation specifications detected during routine stability testing. The recall affects 5,953 cartons distributed nationwide.
Golden State Medical Supply Inc. is recalling Alprazolam Tablets, USP 1mg (180-count bottles, Lot #GS027852) due to potential cross-contamination with other drug substances during manufacturing.
CellEra LLC is recalling Vitale Silver calcium alginate dressings nationwide because packages contain incorrect Instructions for Use with language not approved by the FDA. The firm is providing replacement packages with corrected instructions.
Microbiologics Inc is recalling Mycoplasma genitalium Control Panel units that did not undergo proper release testing before distribution. Affected lots were distributed across the U.S. and internationally.
Microbiologics Inc recalls LYFO Disk lot 983-40-3 because it is labeled as Candida tropicalis but actually contains Yersinia enterocolitica. The mislabeling may cause laboratory quality control failures and delayed test results.
PS Seasoning & Spices, Inc. recalled Maplewood Meats Honey BBQ Stick Seasoning (lot 2022-53578) for undeclared wheat. The product was distributed across multiple U.S. states and Canada; consumers with wheat allergies should not use it.
Tony's Tejas Salsa is recalling Port City Soups Thai Green Curry (32oz glass jars) because the production process has not been approved for acidified foods. The product was distributed in Alabama, Louisiana, Mississippi, and Tennessee.
PS Seasoning & Spices, Inc. is recalling WAP Honey BBQ Seasoning because it contains undeclared wheat. Consumers with wheat allergies should not consume this product.
Tony's Tejas Salsa is recalling Port City Soups Tex-Mex Chili because the production process was not approved for acidified foods. The recall affects 81 units distributed in Alabama, Louisiana, Mississippi, and Tennessee.
CellEra LLC is recalling Vitale Silver calcium Alginate Dressings because product packages contain incorrect Instructions for Use with language beyond FDA 510(k) clearance scope. The firm is replacing affected units with correct instructions.
CellEra LLC is recalling Vitale Silver calcium alginate dressings because the included Instructions for Use contain language exceeding FDA clearance. The firm is replacing affected units with correct instructions.
CellEra LLC recalls Vitale Silver calcium Alginate Dressing Ropes due to incorrect Instructions for Use in product packaging. The manufacturer is replacing affected units with corrected instructions.
LeMans is recalling specific replacement laced motorcycle rear wheels because incorrect welding may cause spokes to break, increasing the risk of a crash.
Hi-Tech E.V.S. is recalling 2020 Spartan MetroStar and 2021 Spartan Gladiator emergency vehicles because LCD displays may lock up, potentially delaying emergency efforts.
Marion Body Works is recalling one 2018 International SR525 emergency vehicle because the engine may overcome the parking brake, increasing crash risk.
Heartland is recalling certain 2022 Trail Runner, Prowler, and Lithium travel trailers with defective power inlet bolts that may loosen, creating an electrical fire hazard. Dealers will inspect and replace the inlet free of charge.
ZH Brothers is recalling Epicord 50-amp Shore Power Inlets because loose wiring connections may cause electrical arcs or shorts, increasing the risk of fire.
Mercedes-Benz is recalling specific 2007-2014 models because incorrect software updates may cause loss of drive power or control functions, increasing crash risk.
Mercedes-Benz is recalling 2021 S 500/S 580 and 2022 EQS 450/580 vehicles because a software error may disable rear turn signals, hazard lights, and reverse lights.
Midwest Motorsports is recalling Kylin K77 helmets in sizes L, XL, and XXL because they may not adequately protect the wearer in a crash.
Dometic is recalling specific 2-burner cooktops because damaged burner control valves may cause a gas leak, increasing the risk of fire.
Tesla is recalling certain Model 3, S, and X vehicles because the rearview camera image may not display immediately when reversing, increasing crash risk.
HD Premier is recalling DigitDots 3mm and 5mm magnetic balls because swallowed magnets can lodge in the digestive system, causing perforation, blockage, infection, and potentially death. Four children have required surgery to remove ingested DigitDots.
FXswede AB is recalling about 5,000 ToolGuards Portable Water Immersion Heaters sold on Amazon.com because the units can overheat, melt, or catch fire, creating electrocution and fire hazards. The firm has received 19 reports of overheating or fires and 2 reports of consumer shock.
Newmar is recalling 1,277 of its 2021 and 2022 motorhomes because the steering column bolt may not be properly tightened, potentially causing loss of steering control. Owners should contact dealers for free inspection and tightening.
Acme United is recalling PhysiciansCare brand over-the-counter pain relievers and aspirin because the packaging is not child-resistant as required by law, creating a poisoning risk for young children.
Navistar is recalling 2018-2023 International LT vehicles with 1500W Purkeys inverter systems. The positive battery cable may be incorrectly routed, causing it to chafe and become damaged, which increases the risk of electrical fire.
General Motors is recalling 2014-2015 Chevrolet Equinox and GMC Terrain vehicles because corroded ball joints may cause windshield wipers to fail, reducing visibility.
Abbott Laboratories is recalling 22,074 cases of Similac for Supplementation infant formula due to potential Cronobacter sakazakii and Salmonella Newport contamination identified through consumer complaints and manufacturing facility testing.
Abbott Similac For Spit Up Infant Formula with Iron is recalled due to consumer complaints of Cronobacter sakazakii and Salmonella Newport, with evidence of Cronobacter sakazakii found in the manufacturing facility.
Abbott Similac Pro-Advance infant formula is being recalled due to potential contamination with Cronobacter sakazakii and Salmonella Newport. The FDA Class I recall affects products distributed nationwide and worldwide.
Abbott Similac Pro-Total Comfort Infant Formula is being recalled due to potential contamination with Cronobacter sakazakii and Salmonella Newport. Consumer complaints have been linked to these dangerous pathogens in affected infants.
Abbott is recalling EleCare Junior Vanilla infant formula due to possible contamination with Cronobacter sakazakii or Salmonella Newport. The company found evidence of Cronobacter in the manufacturing facility and received consumer complaints.
Abbott is recalling Similac For Spit Up Infant Formula due to contamination risks. Consumer complaints linked the product to Cronobacter sakazakii and Salmonella Newport, and Cronobacter was found in the manufacturing facility.
Abbott is recalling Similac Sensitive Infant Formula with Iron due to potential Cronobacter sakazakii and Salmonella Newport contamination linked to consumer complaints about infant illness. The FDA classified this as a Class I recall.
Abbott is recalling Similac Alimentum infant formula due to consumer complaints of Cronobacter sakazakii and Salmonella Newport contamination, with evidence of Cronobacter in the manufacturing facility. The recall affects 40,943 cases.
Abbott is recalling Similac infant formula products for possible contamination with Cronobacter sakazakii and Salmonella Newport following consumer complaints of illness in infants.
Abbott Similac Alimentum Toddler Drink is recalled for consumer complaints related to Cronobacter sakazakii or Salmonella Newport contamination in infants, with Cronobacter sakazakii evidence found in the manufacturing facility.
Abbott is recalling EleCare Jr infant nutrition powder (203,416 cases) due to consumer complaints of Cronobacter sakazakii and Salmonella Newport in infants and contamination found in the manufacturing facility.
Abbott Similac Pro-Sensitive Infant Formula is being recalled due to consumer complaints of Cronobacter sakazakii and Salmonella Newport in infants, with evidence of Cronobacter found in the manufacturing facility.
Abbott recalls Similac Advance Step-1 infant formula due to Cronobacter sakazakii and Salmonella Newport detected in the product and manufacturing facility, following consumer complaints in infants.
Abbott Similac PM 60/40 Low Iron Infant Formula has been recalled due to contamination with Cronobacter sakazakii and Salmonella Newport. The recall affects 8,358 cases distributed nationally and worldwide.
Abbott Similac Organic infant formula products are recalled by the FDA due to potential Cronobacter sakazakii or Salmonella Newport contamination. Consumer complaints of illness in infants and manufacturing facility contamination triggered this Class I recall.
Nature's Eats Balance Hearty Mix 16 oz is being recalled because it contains undeclared milk, a common allergen. The voluntary FDA Class I recall affects 13,656 cases distributed across 21 states.
Abbott Similac Total Comfort Infant Formula with Iron is being recalled due to consumer complaints related to Cronobacter sakazakii and Salmonella Newport. The FDA classified this Class I recall affecting over 1.2 million cases.
Abbott Laboratories is recalling Alimentum infant formula due to Cronobacter sakazakii detected in the manufacturing facility and consumer complaints of Cronobacter and Salmonella Newport in infants.
Abbott is recalling Similac infant formula due to possible contamination with Cronobacter sakazakii and Salmonella Newport. The recall covers approximately 103,025 cases distributed nationwide and worldwide.
Abbott is recalling Similac Pro-Advance infant formula due to potential contamination with Cronobacter sakazakii and Salmonella Newport. Consumer complaints related to these pathogens in infants have been reported, and the bacteria was found in the manufacturing facility.
Abbott is recalling Similac Sensitive infant formula due to potential contamination with Cronobacter sakazakii or Salmonella Newport. Consumer complaints related to these pathogens in infants and evidence of Cronobacter in the facility prompted the Class I recall.
Abbott Similac Pro-Advance Infant Formula is being recalled due to potential Cronobacter sakazakii and Salmonella Newport contamination. The FDA Class I recall affects approximately 1.7 million cases distributed nationwide and worldwide.
Concord Farms is recalling Fresh Enoki Mushrooms due to Listeria monocytogenes contamination found by the California Department of Public Health. The affected product was distributed in California and Nevada.
Abbott is recalling Similac Alimentum infant formula due to consumer complaints involving Cronobacter sakazakii and Salmonella Newport bacteria. The bacteria were found in some products and in the manufacturing facility.
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