Recalls in April 2026 (page 6)
673 recalls.
- DELFLEX recall (Fresenius Medical Care Holdings, Inc.)
DrugClass IIReported May 13, 2026 · Lack of Assurance of Sterility: Potential leaks from perforations in bags. - DELFLEX recall (Fresenius Medical Care Holdings, Inc.)
DrugClass IIReported May 13, 2026 · Lack of Assurance of Sterility: Potential leaks from perforations in bags. - busPIRone Hydrochloride Tablets recall (Unichem Pharmaceuticals USA Inc.)
DrugClass IIIReported May 13, 2026 · Subpotent drug - One Step P in vitro diagnostic test REF: 8194 recall (DFI Co., Ltd.)
Medical deviceClass IIReported May 13, 2026 · The devices were distributed without required FDA premarket clearance or approval. - One Step K in vitro diagnostic test REF: 81A4 recall (DFI Co., Ltd.)
Medical deviceClass IIReported May 13, 2026 · The devices were distributed without required FDA premarket clearance or approval. - Uric Acid in vitro diagnostic test REF: 31H0P recall (DFI Co., Ltd.)
Medical deviceClass IIReported May 13, 2026 · The devices were distributed without required FDA premarket clearance or approval. - QUCARE Total Cholesterol in vitro diagnostic test REF: 6407 recall (DFI Co., Ltd.)
Medical deviceClass IIReported May 13, 2026 · The devices were distributed without required FDA premarket clearance or approval. - One Step pH in vitro diagnostic test REF: 31I4P recall (DFI Co., Ltd.)
Medical deviceClass IIReported May 13, 2026 · The devices were distributed without required FDA premarket clearance or approval. - One Step UTI in vitro diagnostic test REF: 3374 recall (DFI Co., Ltd.)
Medical deviceClass IIReported May 13, 2026 · The devices were distributed without required FDA premarket clearance or approval. - One Step 10A in vitro diagnostic test recall (DFI Co., Ltd.)
Medical deviceClass IIReported May 13, 2026 · The devices were distributed without required FDA premarket clearance or approval. - Biofire Spotfire Respiratory/Sore Throat Panel REF: 423485 recall (BioFire Diagnostics, LLC)
Medical deviceClass IIReported May 13, 2026 · Respiratory/sore throat panel test may result in false negative results and control failures. - BioFire Joint Infection recall (BioFire Diagnostics, LLC)
Medical deviceClass IIReported May 13, 2026 · Contamination to in-vitro diagnostic test may result in false positives. - LIFEPAK 15 recall (Physio-Control, Inc.)
Medical deviceClass IIReported May 13, 2026 · Some defibrillators serviced between July 2023 through November 2025 were serviced without objective evidence that a Performance Inspection Procedure (PIP) was... - Brand Name: Da Vinci X and Da Vinci Xi Product Name: da Vinci X recall (Intuitive Surgical, Inc.)
Medical deviceClass IIReported May 13, 2026 · Due to manipulator containing screws with in the arm sub-assembly that my be susceptible to breaking. - Beacon Tip Centimeter Sizing Catheter RPN/GPN NR5.0-35-70-P-10S-0-CSC-20 G31213 ... recall (Cook Incorporated)
Medical deviceClass IReported May 13, 2026 · Marker bands may be at an increased risk of cracking/breakage. Potential adverse events that may result include increased procedural time, harms associated... - Aurous Centimeter Sizing Catheter RPN N5.0-35-100-P-10S-PIG-CSC-20-01 GPN G47308 ... recall (Cook Incorporated)
Medical deviceClass IReported May 13, 2026 · Marker bands may be at an increased risk of cracking/breakage. Potential adverse events that may result include increased procedural time, harms associated... - Centimeter Sizing Catheter RPN N5.0-35-100-P-10S-PIG-CSC-20 GPN G11916 Catheters... recall (Cook Incorporated)
Medical deviceClass IReported May 13, 2026 · Marker bands may be at an increased risk of cracking/breakage. Potential adverse events that may result include increased procedural time, harms associated... - Black label with blue lettering. FOOD Korean Food recall (HEMU TRADING INC)
FoodClass IReported May 6, 2026 · product tested positive for Listeria Monocytogenes. - Calypso Tropic Tango Lemonade. 16 FL oz recall (King Juice Company, Inc.)
FoodClass IIReported May 6, 2026 · Product contains undeclared Yellow No. 5. - My Mochi Strawberry flavored Non-Dairy Frozen Dessert recall (The Mochi Ice Cream Company, LLC)
FoodClass IIReported May 6, 2026 · Foreign object found inside retail container. - Specially SELECTED brand Vanilla Creme Brulee recall (LACTALIS CANADA, INC)
FoodClass IIReported May 6, 2026 · Product may contain foreign objects, specifically glass. - Negita Cracker- Shrimp 2.8oz recall (Hadson (Toko) Trading Co. Inc.)
FoodClass IIReported May 6, 2026 · Contains undeclared FD&C Yellow 6 - 52USA brand POPPING BOBA recall (Guangdong Zonegoing Food Co., LTD)
FoodClass IIReported May 6, 2026 · Products contain unapproved colors, specifically tartrazine (FD&C Yellow 5), sunset yellow (FD&C Yellow 6), and allura red (FD&C Red 40). - 52USA brand POPPING BOBA recall (Guangdong Zonegoing Food Co., LTD)
FoodClass IIReported May 6, 2026 · Products contain unapproved colors, specifically tartrazine (FD&C Yellow 5), sunset yellow (FD&C Yellow 6), and allura red (FD&C Red 40). - 52USA brand POPPING BOBA recall (Guangdong Zonegoing Food Co., LTD)
FoodClass IIReported May 6, 2026 · Products contain unapproved colors, specifically tartrazine (FD&C Yellow 5), sunset yellow (FD&C Yellow 6), and allura red (FD&C Red 40). - Alendronate Sodium Oral Solution recall (Hikma Pharmaceuticals USA INC)
DrugClass IIReported May 6, 2026 · This recall is being conducted due to out of specification assay results in a limited number of bottles that were stored on side. - Lidocaine Wound Gel recall (Water-Jel Technologies, LLC)
DrugClass IIIReported May 6, 2026 · Failed PH Specifications - fentaNYL Citrate Injectable Solution in 0.9% Sodium Chloride recall (Wells Pharma of Houston LLC)
DrugClass IIReported May 6, 2026 · cGMP deviations. - Ketamine Hydrochloride Injectable Solution recall (Wells Pharma of Houston LLC)
DrugClass IIReported May 6, 2026 · cGMP deviations. - fentaNYL Citrate Injectable Solution in 0.9% Sodium Chloride recall (Wells Pharma of Houston LLC)
DrugClass IIReported May 6, 2026 · cGMP deviations. - fentaNYL Citrate Injectable Solution recall (Wells Pharma of Houston LLC)
DrugClass IIReported May 6, 2026 · cGMP deviations. - fentaNYL Citrate injectable Solution in 0.9% Sodium Chloride recall (Wells Pharma of Houston LLC)
DrugClass IIReported May 6, 2026 · cGMP deviations. - fentaNYL Citrate Injectable Solution recall (Wells Pharma of Houston LLC)
DrugClass IIReported May 6, 2026 · cGMP deviations. - Phenylephrine Hydrochloride Injectable Solution recall (Wells Pharma of Houston LLC)
DrugClass IIReported May 6, 2026 · cGMP deviations. - Similasan recall (Thea Pharma, Inc.)
DrugClass IIReported May 6, 2026 · Lack of Assurance of Sterility: This recall has been initiated due to CGMP deviations found by the FDA during an inspection of the manufacturer. - iVIZIA recall (Thea Pharma, Inc.)
DrugClass IIReported May 6, 2026 · Lack of Assurance of Sterility: This recall has been initiated due to CGMP deviations found by the FDA during an inspection of the manufacturer. - Optase Dry Eye Intense Drops recall (SCOPE HEALTH)
DrugClass IIReported May 6, 2026 · Lack of Assurance of Sterility - Levocarnitine Injection recall (American Regent, Inc.)
DrugClass IIIReported May 6, 2026 · Labeling: Missing Label - GenTeal Tears recall (Alcon Research LLC)
DrugClass IIReported May 6, 2026 · Lack of Assurance of Sterility: Due to FDA inspection observations that it believes may impact product quality. - Systane recall (Alcon Research LLC)
DrugClass IIReported May 6, 2026 · Lack of Assurance of Sterility: Due to FDA inspection observations that it believes may impact product quality. - epoc BGEM BUN Test Card recall (Siemens Healthcare Diagnostics Inc)
Medical deviceClass IIReported May 6, 2026 · Use of the affected product can result in discrepant low pH and measured Total Carbon Dioxide (mTCO2) results and corresponding calculated values in arterial... - Philips Bridge Prep Kit REF: K12-09098C Sterile EO recall (Merit Medical Systems, Inc.)
Medical deviceClass IIReported May 6, 2026 · catheter may experience resistance when being advanced over the guidewire - Philips Bridge Prep Kit REF: K12-09098C Sterile EO recall (Merit Medical Systems, Inc.)
Medical deviceClass IIReported May 6, 2026 · catheter may experience resistance when being advanced over the guidewire - Philips Bridge Prep Kit REF: K12-09098B Sterile EO recall (Merit Medical Systems, Inc.)
Medical deviceClass IIReported May 6, 2026 · catheter may experience resistance when being advanced over the guidewire - i-STAT G3+ cartridge recall (Abbott Point Of Care Inc.)
Medical deviceClass IIReported May 6, 2026 · Approximately 7.6% of cartridges from specific i-STAT EG7+ (list number 03P76-25), i-STAT EG6+ (list number 03P77-25) and i-STAT G3+ (list number 03P78-26)... - i-STAT EG6+ cartridge recall (Abbott Point Of Care Inc.)
Medical deviceClass IIReported May 6, 2026 · Approximately 7.6% of cartridges from specific i-STAT EG7+ (list number 03P76-25), i-STAT EG6+ (list number 03P77-25) and i-STAT G3+ (list number 03P78-26)... - i-STAT EG7+ cartridge recall (Abbott Point Of Care Inc.)
Medical deviceClass IIReported May 6, 2026 · Approximately 7.6% of cartridges from specific i-STAT EG7+ (list number 03P76-25), i-STAT EG6+ (list number 03P77-25) and i-STAT G3+ (list number 03P78-26)... - Depuy Synthes recall (DEPUY (IRELAND))
Medical deviceClass IIReported May 6, 2026 · The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility. - Depuy Synthes recall (DEPUY (IRELAND))
Medical deviceClass IIReported May 6, 2026 · The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility. - Depuy Synthes recall (DEPUY (IRELAND))
Medical deviceClass IIReported May 6, 2026 · The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility. - Depuy Synthes recall (DEPUY (IRELAND))
Medical deviceClass IIReported May 6, 2026 · The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility. - Depuy Synthes recall (DEPUY (IRELAND))
Medical deviceClass IIReported May 6, 2026 · The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility. - Depuy Synthes recall (DEPUY (IRELAND))
Medical deviceClass IIReported May 6, 2026 · The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility. - Depuy Synthes recall (DEPUY (IRELAND))
Medical deviceClass IIReported May 6, 2026 · The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility. - Depuy Synthes recall (DEPUY (IRELAND))
Medical deviceClass IIReported May 6, 2026 · The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility. - Depuy Synthes recall (DEPUY (IRELAND))
Medical deviceClass IIReported May 6, 2026 · The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility. - BD GasPak EZ Campy Pouch System. Catalog Number: 260685. for microbiologic use recall (Becton Dickinson & Co.)
Medical deviceClass IIReported May 6, 2026 · BD identified an issue affecting certain lots of BD GasPak EZ CO2 and BD GasPak EZ Campy Gas Generating Pouch Systems, where gas generating sachets may produce... - BD GasPak EZ CO2 Pouch System. Catalog Number: 260684. for microbiologic use recall (Becton Dickinson & Co.)
Medical deviceClass IIReported May 6, 2026 · BD identified an issue affecting certain lots of BD GasPak EZ CO2 and BD GasPak EZ Campy Gas Generating Pouch Systems, where gas generating sachets may produce... - Philips Upgrade to MR 7700 with MR Elastography recall (Philips North America)
Medical deviceClass IIReported May 6, 2026 · The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading... - Philips SmartPath to Ingenia Elition X with MR Elastography recall (Philips North America)
Medical deviceClass IIReported May 6, 2026 · The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading... - Philips SmartPath to dStream for XR and 3.0T with MR Elastography recall (Philips North America)
Medical deviceClass IIReported May 6, 2026 · The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading... - Philips SmartPath to dStream for 3.0T with MR Elastography recall (Philips North America)
Medical deviceClass IIReported May 6, 2026 · The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading... - Philips SmartPath to dStream for 1.5T with MR Elastography recall (Philips North America)
Medical deviceClass IIReported May 6, 2026 · The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading... - Philips MR 7700 with MR Elastography recall (Philips North America)
Medical deviceClass IIReported May 6, 2026 · The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading... - Philips Ingenia Elition X with MR Elastography recall (Philips North America)
Medical deviceClass IIReported May 6, 2026 · The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading... - Philips Ingenia Elition S with MR Elastography recall (Philips North America)
Medical deviceClass IIReported May 6, 2026 · The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading... - Philips Ingenia Ambition X with MR Elastography recall (Philips North America)
Medical deviceClass IIReported May 6, 2026 · The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading... - Philips Ingenia Ambition S with MR Elastography recall (Philips North America)
Medical deviceClass IIReported May 6, 2026 · The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading... - Philips Ingenia 3.0T CX with MR Elastography recall (Philips North America)
Medical deviceClass IIReported May 6, 2026 · The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading... - Philips Ingenia 3.0T with MR Elastography recall (Philips North America)
Medical deviceClass IIReported May 6, 2026 · The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading... - Philips Ingenia 1.5T CX with MR Elastography recall (Philips North America)
Medical deviceClass IIReported May 6, 2026 · The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading... - Philips Ingenia 1.5T with MR Elastography recall (Philips North America)
Medical deviceClass IIReported May 6, 2026 · The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading... - Philips Evolution upgrade 3.0T with MR Elastography recall (Philips North America)
Medical deviceClass IIReported May 6, 2026 · The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading... - Philips Evolution Upgrade 1.5T with MR Elastography recall (Philips North America)
Medical deviceClass IIReported May 6, 2026 · The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading... - Philips Achieva 3.0T with MR Elastography recall (Philips North America)
Medical deviceClass IIReported May 6, 2026 · The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading... - Philips Achieva 1.5T Initial system with MR Elastography recall (Philips North America)
Medical deviceClass IIReported May 6, 2026 · The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading... - Philips Achieva 1.5T with MR Elastography recall (Philips North America)
Medical deviceClass IIReported May 6, 2026 · The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading... - American Honda Motor Recalls Off-Road Motorcycles Due to Risk of Serious Injury or Death Due to Crash Hazard
Consumer productReported May 1, 2026 · The handlebar's clamp can unexpectedly cause the handlebar to rotate, posing a risk of serious injury or death due to a crash hazard. - Build-A-Bear Workshop Recalls Heartwarming Hugs Bears Due to Risk of Serious Injury or Death from Choking Hazard to Children
Consumer productReported May 1, 2026 · The zipper slider on the side pouch can detach, posing a risk of serious injury or death from choking hazard to children. - CBC Group Recalls Stephan Baby Boo Bunnie and Friends Children's Toys Due to Risk of Serious Injury from Choking and Laceration Hazards
Consumer productReported May 1, 2026 · The toys' plastic cube can break into small parts or sharp edges, posing a risk of serious injury from choking and laceration hazards. - Bayer Recalls 6 mL Size Afrin Original Nasal Spray Bottles Due to Risk of Serious Injury or Illness from Child Poisoning; Violates Mandatory Standard for Child-Resistant Packaging
Consumer productReported May 1, 2026 · The 6 mL nasal sprays contain an imidazoline, which must be in child-resistant packaging or meet the labeling requirements for non-complying packaging, as... - Qumeney Bicycle Light Sets Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Consumer Products with Button Cell Batteries; Sold on Amazon by Smfanlus
Consumer productReported May 1, 2026 · The recalled bicycle lights violate the mandatory standard for consumer products with button cell and coin batteries because they contain button cell batteries... - Acer America Corporation Recalls Two-Wheeled Folding Electric Due to Risk of Injury from Fall Hazard
Consumer productReported May 1, 2026 · A loose screw can cause the front tube to fold down unexpectedly, posing a risk of injury from a fall hazard. - Pressure Washers Recalled Due to Serious Risk of Injury or Death from Shock and Electrocution Hazards; Imported by DGIVOVO US
Consumer productReported May 1, 2026 · The recalled pressure washers lack an integral ground-fault circuit-interrupter (GFCI), posing a serious risk of injury or death from shock and electrocution... - Earthtec Pool Drain Covers Recalled Due to Risk of Serious Injury or Death from Entrapment and Drowning Hazards; Violates Virginia Graeme Baker Pool & Spa Safety Act; Manufactured by Tonyidea
Consumer productReported May 1, 2026 · The recalled drain covers violate the entrapment protection standards of the Virginia Graeme Baker Pool and Spa Safety Act (VGBA), posing entrapment and... - Residential Elevators Recalls Elevator StrikeLock Hoistway Door Locking Device Due to Risk of Serious Injury or Death from Fall and Injury Hazards
Consumer productReported May 1, 2026 · The elevator's StrikeLock hoistway door locking device can allow the elevator cab to move with a landing door open, posing a risk of serious injury or death... - Adult Portable Bed Rails Recalled Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violate Mandatory Standard for Adult Portable Bed Rails; Imported by Hepo Care Medical Equipment Online
Consumer productReported May 1, 2026 · The recalled bed rails violate the mandatory standard for adult portable bed rails because users can become entrapped within the bed rail or between the bed... - 5-Drawer Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violates Mandatory Standard for Clothing Storage Units; Imported by UHOMEPRO
Consumer productReported May 1, 2026 · The recalled dressers are unstable if they are not anchored to the wall, posing tip-over and entrapment hazards that can result in risks of serious injuries or... - Malker Bicycle Light Sets Recalled Due to Risk of Serious Injury or Death from Battery Ingestion Hazard; Violates Mandatory Standard for Consumer Products with Button Cell Batteries; Sold on Amazon by MalkerDirect
Consumer productReported May 1, 2026 · The recalled bicycle lights violate the mandatory standard for consumer products with button cell and coin batteries because they contain button cell batteries... - Segmart 4-Drawer Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment; Violate Mandatory Standard for Clothing Storage Units; Sold on Walmart.com by SOFT
Consumer productReported May 1, 2026 · The recalled dressers are unstable if they are not anchored to the wall, posing tip-over and entrapment hazards that can result in risks of serious injuries or... - Alliance Chemical Recalls 1-K Kerosene Heater Fluid Containers Due to Risk of Serious Injury or Death from Flash Fire, Burn and Child Poisoning; Violates Mandatory Standards for Portable Fuel Containers
Consumer productReported May 1, 2026 · The pre-filled fuel containers violate the mandatory safety standards for portable fuel containers because they lack flame mitigation devices required under... - Thermos Recalls 8.2 Million Stainless King Food Jars and Bottles Due to Serious Impact Injury and Laceration Hazards
Consumer productReported May 1, 2026 · If perishable food or beverages are stored in the container for an extended period of time, the stopper can forcefully eject when opened, which can result in... - Kirkland Signature Traditional Madeleines 12 Count/net wt. 18oz. recall (Costco Wholesale Corporation)
FoodClass IReported April 29, 2026 · Undeclared hazelnut and soy lecithin. - EL MEXICANO agua fresca de horchata Instant Horchata Drink recall (Marquez Brothers International, Inc.)
FoodClass IIReported April 29, 2026 · Undeclared milk. - EL MEXICANO horchata casera Instant Horchata Drink recall (Marquez Brothers International, Inc.)
FoodClass IIReported April 29, 2026 · Undeclared milk. - Bulk Horchata Powder 3951 recall (Marquez Brothers International, Inc.)
FoodClass IIReported April 29, 2026 · Undeclared milk. - Claravis recall (Teva Pharmaceuticals USA, Inc)
DrugClass IIReported April 29, 2026 · Failed Impurities/Degradation Specifications: Out of specification for specific impurity Tretinoin - LACTATED RINGER'S IRRIGATION recall (B BRAUN MEDICAL INC)
DrugClass IIReported April 29, 2026 · Lack of Assurance of Sterility; potential for leakage from the diaphragm port once the foil is removed. - 0.9 % SODIUM CHLORIDE IRRIGATION recall (B BRAUN MEDICAL INC)
DrugClass IIReported April 29, 2026 · Lack of Assurance of Sterility; potential for leakage from the diaphragm port once the foil is removed. - DEXTROSE INJECTION USP recall (B BRAUN MEDICAL INC)
DrugClass IIReported April 29, 2026 · Lack of Assurance of Sterility; potential for leakage from the diaphragm port once the foil is removed.