Archive
561 recalls were announced in July 2022.
Of the 561 recalls this month scored against our rubric, 1% are Critical, 17% are Severe.
Which agencies issued them
Covidien recalls 25,765 Palindrome Precision HSI Chronic Catheters due to a defect in the hub that may cause unintended fluid leakage during dialysis treatment.
Covidien is recalling Mahurkar Chronic Carbothane dialysis catheters due to a potential leaking condition in the hub that may cause unanticipated fluid return during use. Approximately 132,443 units distributed worldwide are affected.
Covidien is recalling certain Palindrome Precision H Chronic Catheters because the hub may leak, causing unexpected fluid to flow back during use. This FDA Class I recall affects 26,675 units distributed globally.
Covidien recalls Palindrome Precision SI chronic dialysis catheters due to a potential leaking condition in the hub that may cause unanticipated fluid return during use.
Giant Eagle brand mini chocolate gobs with peanut butter icing are being recalled due to potential Salmonella contamination from Jiff peanut butter used in manufacturing. The product was distributed in Pennsylvania.
Giant Eagle Brownie Classic Peanut Butter is recalled due to potential Salmonella contamination from the Jiff Peanut Butter ingredient. Affected product distributed in Pennsylvania.
Giant Eagle is recalling Peanut Butter Fudge Bar Cake made with Jiff Peanut Butter due to potential Salmonella contamination. The affected product was distributed in Pennsylvania.
Giant Eagle's Brownie Tray Classic brownies made with Jiff Peanut Butter are being recalled due to potential Salmonella contamination. The product was distributed in Pennsylvania.
Giant Eagle Petite Cake Peanut Butter 18Oz, distributed in Pennsylvania, is recalled due to potential Salmonella contamination. Products were manufactured using Jiff Peanut Butter.
American Contract Systems is recalling 274,400 Clean Catch Urine Kits due to improper assembly by potentially untrained individuals. The FDA classified this as a Class I recall.
Covidien is recalling Palindrome Chronic Catheters due to a potential leaking condition in the hub that may cause unexpected fluid return during use.
Arcoma AB recalls 47 Omnera 400A Digital Radiographic Systems due to potential electrical short circuits that could cause uncontrolled movement of the overhead tube crane.
The FDA has recalled Boric Acid 600 mg capsules (Lot #000-03868160, Exp: 09/14/22) manufactured by Wedgewood Village Pharmacy due to insanitary conditions and lack of processing controls observed during FDA inspection. The recalled product was distributed nationwide.
Siemens is recalling the Dimension LTNI cardiac troponin-I test due to positive bias in Lithium Heparin plasma samples, which may cause false-positive results and inappropriate medical intervention.
Radiometer Medical is recalling ABL800 Flex Analyzers that may produce biased measurements in sodium, calcium, and potassium levels. Approximately 1,489 analyzers are affected worldwide.
Siemens Dimension CTNI cardiac troponin test is recalled for positive bias (falsely elevated readings) in Lithium Heparin plasma samples, which may lead to misdiagnosis of myocardial infarction.
Menarini Silicon Biosystems is recalling CELLSEARCH Circulating Tumor Cell Kit due to potential false positive results in patient samples. The device may generate unassigned events that could affect diagnostic accuracy.
Paris Brothers Inc recalls Brie D'Amir soft ripened cheese due to Listeria detected in environmental samples. The affected product was distributed to wholesale warehouses and retail food establishments.
Covidien is recalling EEA Autosuture Circular Staplers (25mm) because the staple guide may not be securely attached and could disengage during use, potentially allowing the device to cut tissue without forming staples.
Luminex Corporation is recalling the Verigene CDF Nucleic Acid Test due to potential false negative results caused by the swab's hydrophobic characteristics, which could result in missed positive diagnoses.
Abbott recalls 191 TactiCath cardiac ablation catheters that may display incorrect error messages when connected to the EnSite Precision Navigation System, potentially causing user confusion.
SoDelicious DairyFree Wondermilk Salted Caramel Sundae cones are recalled due to peanut contamination. Some cartons mistakenly contain peanut pieces, posing a serious risk to consumers with peanut allergies.
Chromsystems is recalling MassCheck Amino Acid Acylcarnitines dried blood spot control material due to too-low glycine concentration in batch 2821. The defect was found in units distributed to New York, Ohio, and Connecticut.
Covidien is recalling 2,462 units of Palindrome SI Chronic Catheters due to a potential leaking condition in the hub that may cause unanticipated fluid return during treatment.
Siemens Artis and Artis Q.zeego fluoroscopic X-ray systems may lose stand mobility if the robotic control system's BIOS battery discharges at startup. Field service is required to restore function.
EAT REAL FOOD LLC is recalling Culina Plant Based Yogurt nationwide due to potential glass fragments in the product. Affected units were distributed to all states.
Wedgewood Village Pharmacy is recalling Estriol 1mg/gm Vaginal Cream due to insanitary manufacturing conditions and lack of adequate processing controls identified during FDA inspection. The product was distributed nationwide.
Ossur has recalled 410 Variflex Suba Junior prosthetic feet due to cracking and breaking under impact stress. The device is designed for children and adolescents worldwide.
Paris Brothers Inc is recalling Mild Cheddar Cheese (UPC 033954252225) due to Listeria in environmental samples. The affected lots (05042022 and 05052022) were distributed to wholesalers, retailers, and food service establishments.
Culina Strawberry Rose plant-based yogurt is being recalled because glass may be present in the product. The recall affects 13,725 cases distributed nationwide.
Siemens imaging systems with syngo VE20 software may display CT images mirrored horizontally and vertically when loading Toshiba data, potentially causing misinterpretation of patient positioning and inappropriate treatment.
Fresenius Medical Care recalled NaturaLyte 2301 dialysate in Texas and Louisiana after exposure to below-recommended storage temperatures. The exposure may cause packaging leaks, potentially leading to biological contamination and bloodstream infection risk.
Chromsystems has recalled MassCheck Amino Acid, Acylcarnitines dried blood controls (batch 2821) for insufficient glycine concentration. This may affect laboratory test accuracy.
EAT REAL FOOD LLC is recalling Plant Based Yogurt Culina Peach Cashew due to potential glass contamination. The product was distributed nationwide in 13,725 cases.
GE Centricity Universal Viewer Zero Footprint software can display inaccurate measurements on medical images. This Class II recall affects approximately 1,934 units distributed worldwide.
Paris Brothers Inc recalled Pepper Jack Cheese after environmental samples from the production facility tested positive for Listeria.
EAT REAL FOOD LLC is recalling Culina Plant Based Blueberry Lavender Yogurt due to potential glass fragments. Affected lots were distributed nationwide with best-by dates in October and November 2022.
Milton Creamery Prairie Breeze cheese is being recalled due to environmental samples testing positive for Listeria. The product was distributed to wholesale, retail, and food service locations.
Arcoma AB is recalling 71 Omnera 400T radiographic systems because liquid ingress in the display handles may cause electrical short circuits and uncontrolled movement of the overhead tube crane.
EAT REAL FOOD LLC is recalling Plant Based Yogurt Culina Mango Orange Blossom due to potential glass contamination. The affected lot code is 07422CBCUCYMOB0723 with best-by date 11/13/2022, distributed nationwide.
Milton Creamery Tomato Garlic Cheddar Cheese, made by Paris Brothers Inc, is being recalled because Listeria was detected in environmental samples. The affected product was distributed to wholesale warehouses, grocery stores, and food service establishments.
Bix Produce Company LLC is recalling diced spinach due to plastic contamination. The recall affects 1,181 cases distributed in Wisconsin with use-by dates between January and June 2022.
Paris Brothers Inc is recalling WIEBE DAIRY Raw Milk Cheese because environmental samples tested positive for Listeria. The product was distributed to wholesale and retail locations.
EAT REAL FOOD LLC is recalling Plant Based Yogurt Culina Bourbon Vanilla in 5 oz. glass jars nationwide due to potential glass fragments in the product. Consumers should not consume products with the affected lot codes.
Paris Brothers Inc is recalling Colby Jack Cheese due to environmental samples testing positive for Listeria. Affected product has lot code 05042022 and best-by date of August 3–4, 2022.
Cervasi Pecorino Romano Cheese is being recalled by Paris Brothers Inc due to Listeria contamination detected in environmental samples at the production facility.
Luminex Corporation is recalling VERIGENE Enteric Pathogens tests worldwide due to potential false negative results caused by hydrophobic characteristics of the sampling swab. The defect could lead to missed detection of infections in stool specimens.
Wedgewood Village Pharmacy is recalling Boric Acid 600 mg vaginal suppositories (Lot #000-03843532) nationwide due to insanitary manufacturing conditions and lack of processing controls detected during an FDA inspection. No illnesses have been reported.
Wedgewood Village Pharmacy is recalling Estriol vaginal cream nationwide due to insanitary manufacturing conditions and lack of processing controls identified during an FDA inspection.
Rayner is recalling RayOne intraocular lens injection systems because the outer package is mislabeled and contains a different lens strength than indicated. Approximately 162 devices were distributed in 13 US states.
Siemens is recalling 88 Artis Icono X-ray systems in the U.S. due to increased fan wear that could lead to electrical failure and malfunction of the imaging system during operation.
Golden State Medical Supply is recalling 31,260 bottles of Enalapril Maleate Tablets due to manufacturing practice deviations.
Sun Pharmaceutical is recalling 27 vials of Testosterone Cypionate Injection (200 mg/mL) due to manufacturing deviations caused by abnormal machinery appearance. The recall affects multiple lot numbers distributed nationwide.
DePuy Spine's EIT CIF intervertebral fusion cage (46 units, Part No. CUI8070S) is recalled due to a labeling discrepancy where the outer carton label does not match the labels on the product packaging and patient materials.
Domino Foods Inc is recalling 3,150 bags of 50-pound Domino Light Brown Sugar (product number 403350) due to potential exposure to extraneous material during manufacturing. Affected lots were distributed in NY, NJ, PA, and RI.
Golden State Medical Supply Inc. is recalling Enalapril Maleate 2.5 mg tablets due to Current Good Manufacturing Practice (CGMP) deviations. Approximately 1,471 bottles were distributed nationwide.
Wedgewood Village Pharmacy is recalling Bethanechol Chloride 1mg/ml suspension (lot 000-03715131) due to insanitary conditions and lack of processing controls observed during an FDA inspection.
Wedgewood Village Pharmacy LLC is recalling Doxycycline oral suspension (10 mg/ml, 60 ml bottles) nationwide due to insanitary conditions and lack of processing controls discovered during FDA inspection.
Golden State Medical Supply Inc. is recalling 1,424 bottles of Enalapril Maleate 20 mg tablets due to Current Good Manufacturing Practice deviations. The affected lot numbers have expiration dates ranging from March 2022 to December 2022.
Macleods Pharma USA Inc is recalling Eszopiclone 1 mg tablets due to shortfill—customers reported one to three missing tablets from 30-count bottles. Affected lot BEK2009A (exp. 11/2023) was distributed nationwide and to Puerto Rico.
Golden State Medical Supply Inc. is recalling Enalapril Maleate Tablets due to manufacturing practice deviations. The voluntary recall involves 9,058 units distributed nationwide.
DePuy Spine is recalling 61 units of the EIT CIF cage spinal fusion device due to a labeling mismatch. The outer carton label does not match the labels on the blister packages and patient information labels.
Glenmark Pharmaceuticals is recalling Mometasone Furoate Topical Solution USP 0.1% due to defective containers. Approximately 98,307 packs were distributed nationwide.
Vermeer is recalling 2022 BC1800XL trailers because improper hitch bolts may fail, causing the trailer to separate and increasing crash risk.
USDA issued a public health alert for Trader Joe's Caesar Salad with Chicken because the dressing packets contain undeclared egg. No illnesses have been reported.
Winnebago is recalling 2021-2022 Inspire motorhomes because the step well cover support may be insufficient, potentially causing the step to collapse when stepped on.
Prevost is recalling 30 units of the 2021 X3-45 commuter bus because a bolt securing the rear bench seat was not installed, creating a crash injury risk.
Mercedes-Benz is recalling 1,168 2020 GLC 350 E vehicles because a transmission wiring harness may chafe against the drive shaft, causing loss of drive power and increasing crash risk.
Isuzu is recalling 2022 FTR trucks because a missing parking pawl in the transmission could allow the vehicle to roll away, increasing crash risk.
Daimler Vans USA is recalling 2021 Mercedes-Benz Sprinter 2500 vehicles because an incorrectly connected generator wiring harness may cause an electrical surge, increasing the risk of a fire.
Prevost is recalling 2021-2023 X3-45 commuter buses because a seat retention pin could fail, causing the backrest to collapse and increasing injury risk in a crash.
Eveland is recalling 2022 Scamp travel trailers because damaged burner control valves may cause a gas leak, increasing the risk of fire.
Mercedes-Benz is recalling 8,530 vehicles because a software error may prevent the rearview camera from displaying images, increasing crash risk.
Big Tex Trailer Manufacturing is recalling 2003-2022 16GN trailers with defective spare tire mounts that may detach, creating a road hazard.
Forest River is recalling 2022 Coachmen Catalina travel trailers because incorrect wiring may prevent trailer brakes from activating, increasing crash risk.
Subaru is recalling certain 2020-2021 Outback and Legacy vehicles for a transmission control unit programming error that may cause the drive chain to slip, resulting in loss of drive power and increased crash risk.
Forest River is recalling certain Coachmen Freelander and other motorhomes due to improperly connected LPG service valves that can cause propane leaks and fire risk. Dealers will inspect and replace valves at no cost.
Forest River and related RV manufacturers are recalling 2022 trailers with electric awnings that may separate and drop. This poses an injury risk, and owners should contact the manufacturer for free replacement.
Mitsubishi is recalling certain 2022 Outlander vehicles because the rearview camera may fail to display images due to a software error, reducing rear visibility and increasing crash risk.
Roadtrek motorhomes from 2021-2022 are being recalled due to a potential propane tank connection defect that may cause propane leaks and fire risk. Contact Roadtrek at 1-888-762-3873 for free repairs.
Certain 2022 Coachmen Apex travel trailers have incorrectly wired tail lights that may not illuminate, reducing visibility and increasing crash risk.
Samson International recalls Universal Broadmoore Cayden Gentleman's 9-drawer chests sold at Costco because they can tip over and create entrapment hazards if not anchored to the wall. One tip-over incident involving a child has been reported.
Scholastic is recalling approximately 185,700 Shake Look Touch books because pom poms attached to the books can detach, posing a choking hazard to young children. No injuries have been reported.
BMW is recalling 2022–2023 iX and 2022 i4 vehicles because their central display may fail to show critical safety warnings while in Valet Parking Mode. This can increase crash risk.
Daimler Vans USA is recalling 2016-2018 Mercedes-Benz Metris vans because incorrect tire load labels may lead to overloading and tire failure.
Deere & Company is recalling about 160 John Deere X380 and X390 lawn tractors sold from April to May 2022 because wheel hubs may fail, causing loss of braking and propulsion. One minor injury has been reported.
About 1,100 Fugleman UT10E and UT10X utility terrain vehicles are recalled because the cockpit rear panel can overheat and melt, posing a fire hazard. Consumers should stop using the vehicles and bring them to an authorized dealer for free repair.
USDA FSIS issued a public health alert for Don Panchito rendered pork fat produced without federal inspection. No illnesses have been reported, but consumers should discard the product.
Certain 2020-2022 Ford Escape, 2021-2022 Lincoln Corsair, and 2022 Maverick vehicles may experience engine failure leading to engine compartment fires. Owners should stop immediately if they notice engine noises, power loss, or smoke.
Allergy Bee Gone for Kids Nasal Swab Remedy is recalled due to FDA-confirmed microbial contamination including yeast, mold, and Bacillus cereus. Affected consumers should stop using the product.
Taylor Farms Florida is recalling Wawa Apples & Peanut Butter dipper snack cups due to possible Salmonella contamination in the JM Smucker's Jif peanut butter component. Approximately 7,942 units distributed to Wawa locations in Florida are affected.
Forest River Aurora travel trailers (2021-2022) have a brake system defect where the breakaway switch may be incorrectly wired, preventing trailer brakes from activating. Dealers will provide free inspection and repairs.
Fudgeamentals LLC is recalling PEANUT BUTTER CHOCOLATE FUDGE BITES nationwide due to Salmonella contamination in the peanut butter ingredient. The recall affects 189,096 units.
Stellex/CF Houston, LLC is recalling 134,554 cases of Snack Fresh Apples and Peanut Butter fruit trays (6.5 oz) due to potential Salmonella contamination. Code dates 5/14/21–6/4/22 were distributed across 20 U.S. states.
Stellex/CF Houston is recalling Giant Apples, Pretzels & Celery with peanut butter trays due to potential Salmonella contamination. The recall affects 134,554 cases distributed across 20 states from May 2021 through June 2022.
Fudgeamentals LLC is recalling approximately 189,096 units of Peanut Butter Fudge Bars nationwide because the peanut butter ingredient is contaminated with Salmonella. Consumers should not consume the affected product.
Stellex/CF Houston is recalling Wegmans and Market32 apple, pretzels, and cheese trays with peanut butter due to potential Salmonella contamination. Products were distributed across 20 states from May 2021 to June 2022.
Akcea Therapeutics recalls certain Tegsedi (inotersen) Injection lots due to higher-than-labeled active ingredient content. Affected lots were distributed in Kentucky.
Snack Fresh Apple & Cheese Bites with Crackers are being recalled nationwide due to potential Salmonella contamination. Consumers should not consume the product.
Safeway Fresh Foods recalled 1164 cases of Quick Chek Apples and Peanut Butter Snack Trays due to potential Salmonella contamination in the peanut butter. Affected products have various Best Buy dates from April through June 2022.
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