Archive
639 recalls were announced in July 2026.
Of the 639 recalls this month scored against our rubric, 1% are Critical, 37% are Severe.
Which agencies issued them
Olympus Corporation of the Americas is recalling 10 Olympus 4K UHD LCD Monitors (Model OEV321UH) because the HDMI and DisplayPort connectors may become faulty.
Precision Dose Inc. is recalling Glycopyrrolate Oral Solution (1 mg/5 mL) because the product failed to meet specifications for impurities and degradation.
Medline Industries, LP is recalling specific Medline NEURO PACK convenience kits because they may contain low levels of Bacillus species contamination.
Vintage Roots LLC is recalling Vintage Roots Root Beer Syrup because it contains sassafras bark, which is an unapproved food additive.
Kent Imaging, Inc. is recalling SnapshotGLO Wound Imaging Devices (Models KB100 and KB100AA) because software issues may prevent the device from recharging.
Wilcox Industries Corp. is recalling BOSS Xe family aiming devices to implement a software enhancement designed to increase safety.
Micro Therapeutics, Inc. is recalling Pipeline Flex Embolization Devices because the labels may incorrectly state the implant length.
Micro Therapeutics, Inc. is recalling Pipeline Flex Embolization Devices because the labeled implant length does not match the actual device length.
Boston Scientific is recalling 18 FARASTAR Ablation Generator EU devices due to missing FARAPOINT PFA catheter information in the Instructions For Use.
Ascend Laboratories is recalling 2,717 cartons of Dabigatran Etexilate Capsules, 150 mg, because stability testing found impurities above specification.
AVID Medical, Inc. is recalling certain Halyard EYE PACK convenience kits because the Betadine solution contained within them has an incorrect concentration.
Boston Scientific Corporation is recalling 11 units of FARASTAR PFA Generators and Percutaneous Cardiac Ablation Catheters because the Instructions For Use did not include FARAPOINT PFA catheter information.
Rising Pharma is recalling cyproheptadine hydrochloride syrup due to the presence of precipitate, including crystallization and floating particles in the bottle.
Paragon 28 is recalling specific Phantom Hindfoot TTC/TC Ball Tipped Guide Rods because of complaints regarding breaches in the sterile pouch packaging.
Ascend Laboratories is recalling 1,753 cartons of dabigatran etexilate capsules (lot 25141707) due to out-of-specification results in impurity testing during 12-month stability studies.
FDA is recalling Xylocaine (lidocaine HCl) injections due to the presence of particulate matter, specifically hair found in the product.
Imitation crab sticks made by Shandong Ling Xian Food Co., LTD are being recalled because they contain undeclared sodium tripolyphosphate (STTP), a food additive not listed on the product label.
Island Pacific imitation crab sticks are being recalled because they contain undeclared sodium tripolyphosphate.
Shandong Ling Xian Food Co., LTD is recalling Island Pacific Imitation Crab Flakes because they contain undeclared sodium tripolyphosphate.
Asclemed USA Inc. is recalling 18 Lidolog Kits because the label wrap covers the barcode, making it hard to scan. The recall affects products distributed within the U.S. in Tennessee.
Boston Scientific recalls cardiac ablation generators due to incomplete Instructions For Use that omit information about a compatible catheter.
Supernus Pharmaceuticals is recalling Trokendi XR (topiramate) capsules because they failed dissolution specifications. The recall covers 15,853 bottles distributed nationwide.
Newell Coach Corp. is recalling 2025-2027 P50 coaches because the steer axle air spring base may crack, potentially causing loss of suspension support and increasing crash risk.
Grand Design is recalling 2026 Imagine travel trailers because improperly secured outlet cover screws may contact wiring, increasing the risk of a fire.
Ford is recalling 2023-2025 Mustang Mach E vehicles because rear side quarter window glass trim may detach, creating a road hazard and increasing crash risk.
Ford Motor Company is recalling certain 2021-2023 F-150 and 2023-2026 F-250 SD vehicles because a software error can obstruct the rearview camera image.
Grand Design is recalling 2027 Imagine recreational trailers because an inverter circuit may overheat, increasing the risk of a fire.
Grand Design is recalling 2026-2027 Lineage motorhomes because incorrect rear tire pressure labels may lead to over-inflation and increased crash risk.
PACCAR is recalling 2027 Peterbilt and Kenworth trucks because oil contamination in the power distribution center may cause loss of drive power, ABS, or lighting.
Foretravel is recalling 2025-2027 Realm and Realm Presidential motorcoaches because exterior brake lights may stay on, increasing crash risk.
Jayco is recalling certain 2024-2026 Entegra motorhomes because exterior brake lights may stay on when brakes are not applied, increasing crash risk.
Jayco is recalling 2026 Entegra Anthem motorhomes because the vehicle certification label may list the wrong tire size, which could lead to installing incorrect replacement tires.
Midwest Industries is recalling 2027 Yamaha boat trailers because the tongue may fail during towing, causing the trailer to detach and increasing crash risk.
Maple Leaf Foods Inc. recalls approximately 12,036 pounds of not-ready-to-eat smoked bacon from Canada that was imported without required reinspection. No illnesses or injuries have been reported.
ARBOC is recalling 2017-2026 Spirit of Independence transit buses because incorrect washers on rear spring hanger bolts may cause the hanger to detach, increasing crash risk.
Mercedes-Benz USA, LLC is recalling certain 2020-2026 Mercedes-Benz vehicles because a faulty door lock micro-switch may cause the vehicle to roll away.
Frontrunner is recalling 2025 transit buses because wheelchair retractors may fail to lock, increasing injury risk. Owners will be notified to have parts replaced.
CuddleCubs Creations Baby Highchair Teething Toy Sets are recalled due to pull-string teething toys that violate mandatory toy safety standards. The silicone strings can lodge in a child's throat, creating a risk of choking and respiratory distress.
About 670 Sviyatp pool drain covers sold online violate federal safety standards and pose entrapment and drowning hazards. Consumers should stop using affected pools immediately and contact Sviyatp for a refund.
K&N Engineering is recalling specific K&N and Spectre replacement fuel filters because the O-ring may disintegrate, causing leaks or clogs.
BCI Foods, Inc. is recalling approximately 4,300 pounds of canned chicken noodle soup that was imported from Canada without the required import reinspection. No illnesses or injuries have been reported.
BMW is recalling certain 2020-2026 S 1000 RR motorcycles because vibration may cause ignition lock failure, leading to engine stalls or electrical system failures.
EnHomee 9-Drawer Fabric Dressers sold on Walmart.com pose a risk of serious injury or death from tip-over and entrapment if not anchored to the wall. About 16,809 units are affected.
Romorgniz 12-Drawer Fabric Dressers sold on Amazon pose tip-over and entrapment risks to children if not anchored to the wall. About 10,040 units are affected.
Peony Design has recalled personalized baby bibs and stroller bags sold online because snaps can detach, posing a choking risk to young children. The company is offering refunds.
Aojieni Silicone is recalling about 5,918 Sili Factory Pull String Teething Toys because the silicone strings violate toy safety standards and can lodge in a child's throat, posing a serious choking risk.
Forest River is recalling 2027 travel trailers because the Federal Placard may list an incorrect fresh water tank capacity, which could lead to vehicle overloading.
OeyUoc white pool drain covers sold on Amazon violate safety standards and pose entrapment and drowning risks. About 404 units have been recalled; consumers should stop using them immediately.
Forest River is recalling 2026-2027 Pause and OG Luxury Coach RVs because a rooftop fan circuit board may overheat and cause a fire.
D'Dioses Fresa Leche ice pops may contain undeclared milk, pecans, pistachios, and food colorings (yellow #5 and red #40). The product was distributed in NJ, CT, NY, and PA.
ABIOMED Impella CP Introducer Kit 14Fr is being recalled due to a potential for introducer sheath leakage from under the sheath cap and along hub score lines. The manufacturing defect is not visually detectable by users.
W.Y. Industries, Inc. is recalling WY Duck Sauce packets because the product may contain metal fragments. The recall affects 1,120 cases distributed to New York, New Jersey, Ohio, and Pennsylvania.
Abiomed is recalling Impella 5.5 SmartAssist S2 heart pump sets worldwide due to a potential for introducer sheath leakage from under the sheath cap and along hub score lines that may not be visible to users.
Oscor Inc. is recalling Abiomed REF: 0052-3025 Introducer Kits for Impella heart pump due to potential leakage from the sidearm and hub region. Manufacturing issues may cause the 14Fr and 23Fr introducer sheaths to leak under the sheath cap and along hub score lines.
ABIOMED is recalling Impella CP heart pump sets worldwide due to a potential for introducer sheath leakage from under the sheath cap and along hub score lines in 14Fr and 23Fr introducers. The manufacturing defect is not visually detectable.
Oscor Inc. is recalling Abiomed introducer kits due to manufacturing issues that may cause the 14Fr and 23Fr introducer sheaths to leak. The recall affects approximately 1,332 units distributed in Massachusetts.
Argon Medical Devices is recalling Transvenous Pacing Electrode Trays with Bipolar Balloon Pacing Electrode 5F because kits containing Lidocaine HCL Injection USP did not meet sterility release criteria.
D'Dioses Fruit Pops, Inc. is recalling D'Dioses Guayaba ice pops because they may contain undeclared milk, pecans, pistachios, yellow #5, and red #40. Consumers with allergies or sensitivities to these ingredients should not consume the product.
Argon Medical Devices is recalling T-Lok Bone Marrow Tray kits containing Lidocaine HCL Injection USP 1% because the kits did not meet sterility release criteria.
Abiomed is recalling Impella CP Introducer Kits worldwide due to potential leakage from the introducer sheath that cannot be visually detected by users. The manufacturing defect affects 1,540 units across multiple countries.
D'Dioses Coconut Ice Pops (4 oz) may contain undeclared milk, pecans, pistachios, yellow #5, and red #40. Consumers with allergies or sensitivities to these substances should not consume the product.
D'Dioses Mango Ice Pops (3.7 oz) are being recalled because they may contain undeclared milk, pecans, pistachios, yellow #5, and red #40. Consumers with allergies or sensitivities to these ingredients should not consume the product.
D'Dioses Fruit Pops, Inc. is recalling D'Dioses Nanche ice pops because they may contain undeclared milk, pecans, pistachios, yellow #5, and red #40. The product was distributed in NJ, CT, NY, and PA.
D'Dioses Cookies Cream Ice Pops may contain undeclared milk, pecans, pistachios, yellow #5, and red #40. The product was distributed in NJ, CT, NY, and PA.
Olympus Corporation of the Americas is recalling the Olympus Ellik Evacuator (Model 194) worldwide because certain sterilization parameters in the instructions may not render the device adequately sterile.
Abiomed is recalling the Impella 5.5 Smart Assist Set heart pump due to potential leakage from introducer sheaths. The defect is not visually detectable and affects all affected pump sets worldwide.
ABIOMED Impella CP heart pump sets contain introducers that may leak from under the sheath cap and along hub score lines. These manufacturing defects are not visible during use.
Abiomed is recalling the Impella RP Flex heart pump due to potential introducer sheath leakage from the sheath cap and hub score lines. The manufacturing defect is not visually detectable.
Argon Medical Devices is recalling One-Piece Introducer Tray kits containing Lidocaine HCL Injection because they do not meet sterility release criteria. The kits were distributed nationwide and internationally.
Oscor Inc. is recalling the Abiomed Impella Hemostatic Peel Away Introducer System (23F) due to manufacturing defects that may cause leakage from the sidearm, under the sheath cap, or along the hub region.
Abiomed is recalling the Impella CP Smart Assist Set due to a potential for introducer sheath leakage from under the sheath cap and along hub score lines in 14Fr and 23Fr introducers. These manufacturing issues are not visually detectable.
Chiesi USA, Inc. is recalling Cleviprex (clevidipine) injectable emulsion due to lack of assurance of sterility. The affected product is distributed nationwide.
Argon Medical Devices is recalling an Arterial Line Kit containing Lidocaine HCL Injection USP because the kits do not meet sterility release criteria, creating a risk of infection from non-sterile medical injection.
Argon Medical Devices is recalling Bone Marrow Tray kits containing Lidocaine HCL Injection because they do not meet sterility release criteria.
Abiomed is recalling the Impella CP heart pump set (87,277 units worldwide) due to potential leakage from the introducer sheath that cannot be visually detected by users. The defect affects the 14Fr and 23Fr introducers included in every pump set.
ICU Medical is recalling Plum Duo Infusion Pump v1.2.3 units due to a software defect that may cause the pump to deliver up to twice the programmed volume without decrementing the display, risking patient overdose.
D'Dioses Fruit Pops, Inc. is recalling D'Dioses Grocella Ice Pop (1 bar, 81.7 g) due to undeclared milk, pecans, pistachios, yellow #5, and red #40. The product was distributed in NJ, CT, NY, and PA.
CareFusion 213, LLC is recalling ChloraPrep One-Step (chlorhexidine gluconate and isopropyl alcohol) applicators nationwide because affected units may have open or incomplete seals on the packaging, which could compromise sterility assurance.
Argon Medical Devices is recalling General Biopsy Tray kits containing Lidocaine HCL Injection because the kits do not meet sterility release criteria.
Abiomed, Inc. is recalling ABIOMED Impella CP Introducer Kit 14 Fr units worldwide due to potential introducer sheath leakage from under the sheath cap and along hub score lines. The manufacturing defect is not visually detectable.
Heil is recalling 2025-2026 side loader garbage trucks because water may enter high voltage cabinets, causing electrical shorts, fires, or unexpected shutdowns.
Abiomed is recalling ABIOMED Introducer Kit 23 Fr due to potential sheath leakage from manufacturing defects. The leakage risk is not visually detectable and affects all current batches worldwide.
D'Dioses Fruit Pops, Inc. is recalling D'Dioses Vainilla ice pops because they may contain undeclared milk, pecans, pistachios, yellow #5, and red #40. The products were distributed in NJ, CT, NY, and PA.
D'Dioses Fruit Pops, Inc. is recalling D'Dioses Nuez Ice Pop bars because they may contain undeclared milk, pecans, pistachios, yellow #5, and red #40, which pose a serious health risk to consumers with allergies or sensitivities.
Abiomed, Inc. is recalling ABIOMED Intro Kit heart pump introducer sheaths due to potential leakage from under the sheath cap and along hub score lines. The manufacturing defects are not visually detectable by users.
Abiomed is recalling ABIOMED Insertion Kits due to a potential for introducer sheath leakage from under the sheath cap and along hub score lines. The manufacturing defect is not visually detectable by users.
Frutas y Hortalizas del Sur S.A. is recalling Organic Whole Blueberries due to potential E. coli O145:H28 contamination. Affected product is 10 oz frozen blueberry bags distributed in Florida.
D'Dioses Fruit Pops, Inc. is recalling Ice Pop D'Dioses Limon 4 oz packages because they may contain undeclared milk, pecans, pistachios, yellow #5, and red #40. Consumers with allergies or sensitivities to these ingredients should not consume the product.
Medtronic is recalling its Bio-Medicus Adult Cannula Kit (Product Number 96530-115) used in cardiopulmonary bypass procedures due to the discovery of loose foreign material containing trace levels of blood in two units.
ICU Medical is recalling the Plum Solo Precision IV Pump (v1.0.3) because in specific scenarios, the pump may fail to decrease the displayed volume and could deliver up to twice the programmed medication amount.
GE Medical Systems is recalling certain Optima XR200/220/240amx mobile radiographic systems after column replacements because functional testing of the safety pawl may not have been performed, which could allow the X-ray arm to drop and injure patients.
D'Dioses Fruit Pops, Inc. is recalling D'Dioses Mamey Ice Pop (1 Bar, 81.7 g) because it may contain undeclared milk, pecans, pistachios, yellow #5, and red #40.
D'Dioses Fruit Pops, Inc. is recalling D'Dioses Pistachio Ice Pop (1 Bar, 81.7 g) because it may contain undeclared milk, pecans, pistachios, yellow #5, and red #40.
General Mills is recalling Pillsbury Bread Rolls, Kaiser Roll Dough due to potential foreign glass material in the product. Affected consumers should not consume the product and should contact the company or retailer for a refund.
Olympus is recalling the Toomey Evacuator 50cc with Adaptor (Model 188A) because some sterilization parameters in the instructions may not reliably render the devices sterile.
D'Dioses Tamarindo ice pops may contain undeclared milk, pecans, pistachios, yellow #5, and red #40. Consumers with allergies to these ingredients should not consume the product.
D'Dioses Fruit Pops, Inc. is recalling D'Dioses Arroz con Leche Ice Pops because they may contain undeclared milk, pecans, pistachios, yellow #5, and red #40 that are not listed on the label.
Gellert Global Group is recalling Ruby brand Artichoke Hearts Quartered in cans because glass fragments were found in the product. Consumers should not consume affected items.
Orthofix U.S. LLC is recalling 19 units of Orthofix MINIRAIL orthopedic external fixation devices distributed across the US due to incorrect model labeling that could lead to surgical use of the wrong device.
Maquet Cardiovascular is recalling Vasoview Hemopro 2 devices from Lot 3000547797 due to exposure to out-of-specification sterilization during gamma sterilization. The affected devices may not be properly sterilized.
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