Safety Recalls
RSS ↗15,271 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.
Showing 6,851–6,900 of 15,271
- Class I
Food Recall · May 7, 2025
Organic traditions brand JUMBO PUMPKIN SEEDS; 227 g; 8 oz; Packaged and Distributed by: Advantage Health Matters Inc.; UPC: 6 27733 00175 5Product may be contaminated with Salmonella
- Class II
Medical Device Recall · May 7, 2025
MicroAire Surgical Instruments, LLC
Brand Name: SmartRelease ESTR (Endoscopic soft tissue release system), Onyx Blade Assembly; alternate name: ECTR (Endoscopic Carpal Tunnel Release) System, Onyx Blade Assembly; Common Name: SmaPotential that the blade can unintentionally cut tissue prior to the user deploying the blade.
- Class II
Medical Device Recall · May 6, 2025
PhenoMATRIXAI-powered bacterial culture plate interpretation and workup software does not have Premarket Approval or pre-market notification (510(k)/de novo), so there is potential risk that the colony count and/or morphology information from images may not accurately reflect actual plate and may lead to inaccurate counts and/or morphology characteristics impacting patient diagnosis and subsequent care.
- Class I
Drug Recall · May 6, 2025
EnShiShiXiangNiShangMaoYouXianGongSi
ENDURANCE BOOST WITH HORNY GOAT WEED, 500mg, 20 capsules per carton, VEPEMVA Nutrition Supplement....rgy and Endurance, UPC X004BB9Z8NMarketed without approved NDA/ANDA: The product has been found to be tainted with Sildenafil and Propoxyphenylsildenafil (a sildenafil analogue).
- Class II
Medical Device Recall · May 6, 2025
Olympus Corporation of the Americas
Brand Name: Powered Laser Surgical Instrument Product Name: SOLTIVE Pro SuperPulsed Laser System Model/Catalog Number: TFL-SLS, TFL-SLS-JA (Japan only); Product Description: SOLTIVE Laser Systems uPotential for thermal incident including an unexpected occurrence of smoke, sparks, burning, or unsteady flames during clinical use. The fracturing of the fiber is the cause of, or contributes to, these thermal incidents.
- Class II
Food Recall · May 6, 2025
Supreme Produce Celery & PB Snack Cup. Net Wt: 9oz (225g). Keep Refrigerated. UPC 8 50065-40308 3. GBC Food Services, 14043 Distribution Way, Farmers Branch, TexasForeign Material (plastic)
- Class II
Food Recall · May 6, 2025
Gluten Free Vegan Peanut Butter Jam Cookie, Net Wt. 3.5 oz (200g), packaged individually in plasticUndeclared sesame
- Class II
Medical Device Recall · May 6, 2025
Olympus Corporation of the Americas
Brand Name: Powered Laser Surgical Instrument Product Name: SOLTIVE Premium SuperPulsed Laser System Model/Catalog Number: TFL-PLS, TFL-PLS-JA (Japan only); Software Version: N/A Product DescriptiPotential for thermal incident including an unexpected occurrence of smoke, sparks, burning, or unsteady flames during clinical use. The fracturing of the fiber is the cause of, or contributes to, these thermal incidents.
- Class I
Food Recall · May 6, 2025
TRI-UNION FROZEN PRODUCTS INC DBA CHICKEN OF THE SEA FROZEN FOOD
Frozen Shrimp- packaged in 5lb frozen IQF blocks/4 blocks to a case. Unlabeled generic case packaging reads: "Raw P&D Tail-On White Shrimp" 26/30; Contains: Shrimp (Crustacean) UPC# 1 08432370 0405 5Frozen Raw Peeled & Deveined tail on, shrimp contains undeclared sulfites
- Class II
Medical Device Recall · May 6, 2025
Olympus Corporation of the Americas
Brand Name: Powered Laser Surgical Instrument Product Name: Soltive Reusable Laser Fibers Model/Catalog Number: TFL-FBX150R, TFL-FBX200R, TFL-FBX365R, TFL-FBX550R, TFL-FBX940R, TFL-FBX940R-JA (JapanPotential for thermal incident including an unexpected occurrence of smoke, sparks, burning, or unsteady flames during clinical use. The fracturing of the fiber is the cause of, or contributes to, these thermal incidents.
- Class II
Medical Device Recall · May 6, 2025
Affinity 4 Birthing Bed, Product Codes P3700E100429, P3700E100432, P3700E100433, P3700E100434, P3700E100435, P3700E100436, P3700E100437, P3700E100438, P3700E100439, P3700E100441, P3700E100442, P3700E1There is a potential for improper crimps on the signal wires of the actuators which could result in a loss of ability to lower the bed or the foot section of the bed.
- Class II
Food Recall · May 6, 2025
Supreme Produce Apple & PB Snack Cup. Net Wt: 8oz (226g). Keep Refrigerated. UPC 8 50065-403 1. GBC Food Services, 14043 Distribution Way, Farmers Branch, TexasForeign Material (plastic)
- Unclassified
Vehicle Recall · May 6, 2025
Honda (American Honda Motor Co.)
2025 HONDA CR-V HYBRIDA fuel leak in the presence of an ignition source increases the risk of a fire.
- Unclassified
Vehicle Recall · May 6, 2025
2025 MERCEDES-BENZ EQS SUV 580 4MATICA vehicle that makes an incorrect sound may fail to alert pedestrians of a reversing vehicle, increasing the risk of crash.
- Class II
Food Recall · May 6, 2025
Tortilla de mesa with 12 units per package, Tortilla Pirata with 10 units per package, Tortilla cruda especial with 20 units per package, Tortilla Cruda Pirata with 20 units per packageUndeclared soy allergen
- Class II
Medical Device Recall · May 6, 2025
Olympus Corporation of the Americas
Brand Name: Powered Laser Surgical Instrument Product Name: Soltive SuperPulsed Laser Fibers - Single Use Model/Catalog Numbers: TFL-FBX150BS, TFL-FBX200BS, TFL-FBX150S, TFL-FBX200S, TFL-FBX365S, TFPotential for thermal incident including an unexpected occurrence of smoke, sparks, burning, or unsteady flames during clinical use. The fracturing of the fiber is the cause of, or contributes to, these thermal incidents.
- Class II
Medical Device Recall · May 6, 2025
HardyCHROM CRE, selective and differential culture medium for antimicrobial susceptibility testing, Product Catalog No. G323Identified lots failed incoming quality control testing. Lots exhibited breakthrough growth of Klebsiella pneumoniae.
- Class II
Medical Device Recall · May 5, 2025
Olympus Corporation of the Americas
Olympus EVIS EXERA III Duodenovideoscope. Model Number: TJF-Q190VRecent post-market surveillance data suggests a possible association of higher microbial contamination levels from TJF duodenoscopes when manual cleaning was delayed beyond one hour and a presoak was performed, compared to those TJF duodenoscopes where manual cleaning began within one hour after patient procedure.
- Class II
Medical Device Recall · May 5, 2025
Dexcom G7 iOS Application, Ref: SW12300 used in conjunction with the Dexcom G7 Continuous Glucose Monitoring (CGM) systemA bug in the 2.7.0 version of the G7 iOS App can cause the app to enter a state where it stops updating the estimated glucose value (EGV) and continues to show this stale EGV. If the user is unaware that the EGVs are not being updated and that glucose alerts will not trigger, there is potential for the missed detection of a hyperglycemic or hypoglycemic event or a treatment decision made based off incorrect data. There is no impact to transmitter communication with concurrently connected displays. A concurrently connected receiver, Apple Watch, and/or insulin pump will continue to receive EGVs directly from the transmitter when the app is in the problematic state. There is no impact to Automated Insulin Dosing (AID) therapy as the AID system continues to receive EGVs directly from the transmitter.
- Class II
Medical Device Recall · May 5, 2025
Access Testosterone assay, Catalog Number 33560Inadequate preventative maintenance (PM) performed on the scales of the RPL5 fill line, led to splashing (cross-contamination) between the wells of testosterone reagent packs lot 538081, which could potentially result in up to a 34% increase or a 23% decrease in patient results.
- Unclassified
Vehicle Recall · May 5, 2025
Porsche Cars North America, Inc.
2023 PORSCHE TAYCANAn air bag that fails to deploy during a crash increases the risk of injury.
- Class II
Medical Device Recall · May 5, 2025
ASP Global, LLC. dba Anatomy Supply Partners, LLC.
SAFE-T-FILL Micro Capillary Blood Collection, 125 ¿L Prepared with Dipotassium EDTA Purple, Model: 07 6011; SAFE-T-FILL Micro Capillary Blood Collection, 125 ¿L Prepared with Dipotassium EDTA Self-seAll RAM SAFE-T-FILL Micro Capillary Blood Collection tubes manufactured between July 31, 2023 to February 28, 2025 cause false positive results when used with Magellan Diagnostics LeadCare Testing Systems. False positive lead results may cause delayed results and additional unnecessary testing.
- Class II
Medical Device Recall · May 2, 2025
LifeShield Drug Library Management (DLM), LifeShield Infusion Safety Software SUite v2.1 and v2.2Firm has identified Drug Library Management defects in the software: 1) DLM software does not allow user to create percentage dose rate or rate change values with certain limits, potentially resulting in over-delivery to patient. 2) An unauthorized user may modify and approve a drug library, potentially leading to incorrect program parameters being used for therapy.
- Class II
Drug Recall · May 2, 2025
Empower Clinic Services, LLC dba Empower Pharmacy
Testosterone Cypionate Injection, 200 mg/mL, CIII, Rx Only, 5 mL Sterile Multiple-Dose Vial, Compounded by: Empower Pharmacy, 7601 N Sam Houston Pkwy W Ste 100, Houston, TX, 77064, Phone: (877) 562-85Lack of Assurance of Sterility
- Class I
Food Recall · May 2, 2025
Yellowstone Brown Sugar Molasses Baked Beans, NET WT. 15 OZ (425g), packaged in cans, packed 12 cans per case. UPC: 071846187071; Packaged by: Vietti Foods Inc. Nashville, TN 37203Undeclared allergen (soy) due to mislabeling. Product is labeled as Brown Sugar Molasses Baked Beans, but contains Beef and BBQ Baked Beans. The Beef and BBQ Baked Beans contain soy, which is not declared on the label.
- Class II
Medical Device Recall · May 2, 2025
Healthmark Industries Co., Inc.
Pre-filled Water Syringe, Model Numbers SW-010-100 and SW-010During endoscope surveillance monitoring, a user facility identified contamination from duodenoscope samples that were linked to the Pre-filled Water Syringes as part of their investigation. Healthmark Industries conducted its own investigation and concluded that the Pre-filled Water Syringe had been improperly used outside of the intended purpose.
- Class II
Medical Device Recall · May 2, 2025
Catalog No. 8888160556; Umbilical Vessel Catheter 5 French dual lumenPackaging defect may compromise sterility of the product. Use of a non-sterile product on the patient could lead to infection in neonates.
- Class II
Medical Device Recall · May 2, 2025
Catalog No. 8888160341; Umbilical Vessel Catheter 5 French single lumenPackaging defect may compromise sterility of the product. Use of a non-sterile product on the patient could lead to infection in neonates.
- Class II
Medical Device Recall · May 2, 2025
Catalog No. 8888160648; Umbilical Vessel Catheter 5 French triple lumenPackaging defect may compromise sterility of the product. Use of a non-sterile product on the patient could lead to infection in neonates.
- Class II
Medical Device Recall · May 2, 2025
Brand Name: Canturio¿ Smart Extension Product Name: CSE Implant Model/Catalog Number: 43-5570-030-14 Product Description: Tibial stem extension for use with Zimmer Persona¿ Personalized Knee SystemDue to labeling error. Product incorrectly labeled.
- Unclassified
Vehicle Recall · May 2, 2025
Honda (American Honda Motor Co.)
2025 HONDA PILOTA non-functioning seat belt cannot properly restrain the seat occupant, increasing the risk of injury during a crash.
- Class I
Food Recall · May 2, 2025
President Brand Licorice Plum (8 oz., 227g)Contains undeclared sulfites, undeclared FD&C Yellow 6, and unapproved color: Amaranth (E123).
- Class III
Food Recall · May 2, 2025
Nordic Naturals Zero Sugar Kids Multivitamin Supplement - Gummies (120 gummies/bottle); 12 bottles/caseProduct is mislabeled.
- Class II
Medical Device Recall · May 2, 2025
Catalog No. 8888160119; Umbilical Vessel Catheter Insertion Tray with 2.5 and 5 French UVCsPackaging defect may compromise sterility of the product. Use of a non-sterile product on the patient could lead to infection in neonates.
- Class II
Medical Device Recall · May 2, 2025
Healthmark Industries Co., Inc.
ChannelCheck Convenience Pack, Model Numbers UCC-222CP and UCC-222-ESP (Sample)During endoscope surveillance monitoring, a user facility identified contamination from duodenoscope samples that were linked to the Pre-filled Water Syringes as part of their investigation. Healthmark Industries conducted its own investigation and concluded that the Pre-filled Water Syringe had been improperly used outside of the intended purpose.
- Class II
Medical Device Recall · May 2, 2025
Catalog No. 8888160325; Umbilical Vessel Catheter 2.5 French single lumenPackaging defect may compromise sterility of the product. Use of a non-sterile product on the patient could lead to infection in neonates.
- Class II
Medical Device Recall · May 2, 2025
BD BBL CultureSwab EZ Collection and Transport System, REF 220144, in vitro Diagnostic, SterileR, Rx OnlySwabs for specimen collection may be prone to breakage during product usage.
- Class II
Medical Device Recall · May 2, 2025
Catalog No. 8888160333; Umbilical Vessel Catheter 3.5 French single lumenPackaging defect may compromise sterility of the product. Use of a non-sterile product on the patient could lead to infection in neonates.
- Class II
Medical Device Recall · May 1, 2025
GM Helix Acqua Implant, Article Number: 140.984It is possible that a package labelled as an 11.5 mm implant may contain a 13 mm implant instead.
- Class II
Medical Device Recall · May 1, 2025
Thermo SCIENTIFIC Sensititre Cation Adjusted AutoRead Mueller-Hinton Broth w/ TES w/ Lysed Horse Blood, REF CP11410; invitro diagnostic deviceProduct may have an off color affecting perfomance
- Class II
Medical Device Recall · May 1, 2025
Implant Direct Sybron Manufacturing LLC
The Drill Stop Kit is the version of the Mini Sterilizable Tray that is used to store, sterilize, verify Drill Stop length, and facilitate the mounting/removal of the Drill Stops. The Drill Stop Kit iThe Drill stop kit contains incorrect components.
- Unclassified
Consumer Product Recall · May 1, 2025
Shenzhen Baseus Technology Co. Ltd., of China
Baseus 65W 30000mAh Portable Chargers (model number BS-30KP365)The lithium-ion battery in the recalled portable chargers can overheat, posing a fire hazard.
- Unclassified
Consumer Product Recall · May 1, 2025
Santa Cruz Bicycles LLC, of Santa Cruz, California
Heckler 9 Electric BicyclesThe recalled electric bicycle's lithium-ion battery can overheat, posing a fire hazard.
- Class II
Medical Device Recall · May 1, 2025
GM Helix Acqua Implant, Article Number: 140.985It is possible that a package labelled as an 11.5 mm implant may contain a 13 mm implant instead.
- Class II
Medical Device Recall · May 1, 2025
Civco Medical Instruments Co. Inc.
BX2 Needle Guide, Part Number 644-094, tool for performing needle-guided (or catheter) procedures with the use of diagnostic ultrasound transducersDuring the attachment of the needle guide to the covered probe, the tight tolerance and fit of the needle guide can cause a pinhole breach in the transducer cover when latching the guide in place.
- Unclassified
Consumer Product Recall · May 1, 2025
YuanQuXianXianQiDianZiShangWuYouXianZeRenGongSi, (dba YFLGOTOO), of China
Dlesot Snap Hair ClipsThe painted hair clips contain levels of lead that exceed the federal lead paint ban, posing a lead poisoning hazard to children. Lead is toxic if ingested by young children and can cause adverse health issues.
- Unclassified
Consumer Product Recall · May 1, 2025
Kohl's Inc., of Menomonee Falls, Wisconsin
St. Nicholas Square Christmas Tea Light Candle HoldersThe tea light candle holder can catch on fire, posing a fire and burn hazard.
- Unclassified
Consumer Product Recall · May 1, 2025
Kubota Tractor Corporation, of Grapevine, Texas
Kubota Utility VehiclesThe ball joint connected to the front suspension arm can loosen and separate from the front suspension arm, resulting in the driver losing wheel support of the utility vehicle, posing a crash hazard to consumers.
- Unclassified
Consumer Product Recall · May 1, 2025
SharkNinja Operating LLC, of Needham, Massachusetts
SharkNinja Foodi OP300 Series Multi-Function Pressure CookersThe pressure-cooking lid can be opened during use, causing hot contents to escape, posing a risk of burn injuries to consumers.
- Class I
Medical Device Recall · May 1, 2025
Adult Manual Resuscitator with Medium Adult Mask, Bag REservoir, Filter, Manometer and 7 ft Oxygen Tubing, REF CPRM1116FAffected lots were manufactured with B/V Filter incorrectly attached to the wrong port (patient port instead of the exhalation port). If not noticed prior to patient use, there would be interruption or delay in patient resuscitation, which may lead to life threatening consequences, including hypoxia, hypercapnia, organ failure, and death.