Latest Product Recalls Today

Recent Product Recall Alerts List

Showing 3,926 - 3,950 of 4,622 matching product recalls.

Product Recall	Source	Type	Risk	Date	Action
Olympus Thunderbeat 5 mm, 20 cm, Front-Actuated Grip Type S Firm is initiating a removal due to continued reports of adverse events.	FDA Z-1373-2026	Medical Device	High	Feb 25, 2026 Recall: Oct 22, 2025	Details
MONARCH Platform, Bronchoscopy, Catalog Numbers: MON-000005-01 , MON-000005-01R , MON-000006 , MON-000006-RFB, MON-000008 with software Device for bronchoscopic visualization, patient airway access has software issue: if application restarts after patient-side selection, prior to bronchoscope loading, application will re-initialize to patient-left position; and if right position was previously selected, this may lead to unanticipated robotic arm positioning toward patient-left, may result in contact with patient/endotracheal tube.	FDA Z-1383-2026	Medical Device	High	Feb 25, 2026 Recall: Jan 21, 2026	Details
Teslatome Bipolar Sphincterotomes REF: TESLA-B2535-260 Model Number: G60784 UDI-DI code: 00827002607842 REF: TESLA-B2535-450 Model Number: G60785 UDI-DI code: 00827002607859 These devices are used for cannulation of the ductal system and for sphincterotomy. If preloaded, the device also aids in bridging difficult strictures during ERCP. It is indicated for sphincterotome-aided, wire-guided selective cannulation of the biliary ducts. Due to product that may contain a void in the material that separates the wire guide and cutting wire lumens, which may cause an inappropriate path of current during cutting.	FDA Z-1362-2026	Medical Device	High	Feb 25, 2026 Recall: Dec 18, 2025	Details
Medline Industries IV Administration and Extension Sets: 1) DBD-IV ADMIN SET,60DRP,1NEEDLE-FREE VALV, Model Number: DYNDTB0529; 2) IV ADMIN SET, 10DRP, 1NF, 92, Model Number: DYNDTB1029; 3) DBD-IVEXTSET2.4ML2 NEEDLE-FREEVLVE,35, Model Number: DYNDTB1516; 4) DBD-IV ADMIN SET, 15DRP, 1 INJECT PORT,, Model Number: DYNDTB1530; 5) DBD-IV ADMIN SET, 15DRP, ROLLER CLAMP, 6, Model Number: DYNDTB1539; 6) DBD-IV ADMIN SET, 15DRP, 3 NF, 109, Model Number: DYNDTB1545; 7) IV ADMIN SET, 20DRP, 3 NF, 109, Model Number: DYNDTB2045; 8) DBD-IVADMINSET60DRP2NEEDLE-FREEVLVE96, Model Number: DYNDTB0512; 9) DBD-IVA Under circumstances involving exposure to particular chemicals and mechanical forces, the male luer connectors for the specified IV Administration and Extension sets may leak, crack, and/or break during use, which may result in a delay in patient treatment, blood loss, infection, an air embolism, and/or underdosage of medication.	FDA Z-1366-2026	Medical Device	High	Feb 25, 2026 Recall: Dec 31, 2025	Details
Medline Convenience Kits: 1) ADMIT KIT, Model Number: DYKA1343A Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.	FDA Z-1410-2026	Medical Device	High	Feb 25, 2026 Recall: Jan 7, 2026	Details
Medline Convenience Kits: 1) LVAD DRIVELINE TRAY, Model Number: DM1035; 2) KIT SURG ONC INSERT CENT.VENOU, Model Number: DYKMBNDL43 Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.	FDA Z-1402-2026	Medical Device	High	Feb 25, 2026 Recall: Jan 7, 2026	Details
Olympus Thunderbeat, 5mm, 35 cm, Pistol Grip Firm is initiating a removal due to continued reports of adverse events.	FDA Z-1378-2026	Medical Device	High	Feb 25, 2026 Recall: Oct 22, 2025	Details
Medline Convenience Kits: 1) DRAPE PACK-CHOICE, Model Number: DYNJ63118A Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.	FDA Z-1406-2026	Medical Device	High	Feb 25, 2026 Recall: Jan 7, 2026	Details
Olympus Thunderbeat 5 mm, 45 cm, Front-Actuated Grip Type S Firm is initiating a removal due to continued reports of adverse events.	FDA Z-1371-2026	Medical Device	High	Feb 25, 2026 Recall: Oct 22, 2025	Details
Medline Convenience Kits: 1) KIT ACES INSERT PEG, Model Number: DYKMBNDL130; 2) KIT ACES INSERT PEG, Model Number: DYKMBNDL130A; 3) KIT ACES INSERT PERCUTANEOUS T, Model Number: DYKMBNDL4; 4) NICU LINE CHANGE TRAY, Model Number: LC295; 5) OSC SHERMAN KNEE ARTHRO BASIC, Model Number: DYKM1977C; 6) PICC CATHETER INSERTION TRAY, Model Number: CVI4300 Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.	FDA Z-1401-2026	Medical Device	High	Feb 25, 2026 Recall: Jan 7, 2026	Details
MediHoney Gel with Active Leptospermum Honey. Model/Catalog Numbers: (1) 31805, (2) 31815. MediHoney Gel dressing with Active Leptospermum Honey provides a moist environment conducive to wound healing and is indicated for light to moderately exuding wounds. Potential packaging failures, which could lead to a breach in the sterile barrier.	FDA Z-1363-2026	Medical Device	High	Feb 25, 2026 Recall: Jan 16, 2026	Details
Broviac 4.2 Fr Single-Lumen CV Catheter Cutdown Tray with SureCuff Tissue Ingrowth Cuff Cat 60060 Due to damage to outer tray that can potentially compromise the sterile barrier	FDA Z-1367-2026	Medical Device	High	Feb 25, 2026 Recall: Dec 12, 2025	Details
Medline Convenience Kits: 1) KIT TRIPLE LUMEN INSERTION, Model Number: DYNDM1031A Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.	FDA Z-1407-2026	Medical Device	High	Feb 25, 2026 Recall: Jan 7, 2026	Details
Estrone RIA, REF: DSL8700 The affected Estrone RIA kit lots may rarely give falsely high patient results which might cause Temporary injury of Remote probability. Only in some (very rare) cases may the issue occur.	FDA Z-1369-2026	Medical Device	High	Feb 25, 2026 Recall: Dec 15, 2025	Details
Medline Convenience Kits: 1) KIT SURG ONC EXCISION BREAST, Model Number: DYKMBNDL84A; 2) KIT SURG ONC EXPLORATORY LAP, Model Number: DYKMBNDL87A; 3) CT BIOPSY TRAY, Model Number: DYNDH1143C; 4) BIOPSY SPECIALS PACK, Model Number: DYNDH1873; 5) BIOPSY SPECIALS PACK, Model Number: DYNDH1934; 6) BREAST BIOPSY PACK, Model Number: DYNJ17489I; 7) VOR PACK-LF, Model Number: DYNJ48539; 8) VOR PACK-LF, Model Number: DYNJ48539A; 9) IR BIOPSY PACK, Model Number: DYNJ59897B; 10) BREAST PACK, Model Number: DYNJ82998 Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.	FDA Z-1392-2026	Medical Device	High	Feb 25, 2026 Recall: Jan 7, 2026	Details
Woodland Gourmet Arrowroot Flour item code H59EE86, Net Wt. 55 lb., bag in box Possible presence of Foreign Material	FDA H-0515-2026	Food	High	Feb 25, 2026 Recall: Jan 16, 2026	Details
Brass Tope. Sticker label: $29.99+TAX Potential contamination with leachable lead.	FDA H-0512-2026	Food	High	Feb 25, 2026 Recall: Nov 21, 2025	Details
IKM Aluminum Saucepan 9" with Wooden Handle. Sticker label: ALUMINIUM PAN 2 SIDE POUTED WOODEN HANDLE 9" UPC 7 023672 411878 US $ 17.99 Sticker label: IKM INDIAN KITCHEN MART Potential contamination with leachable lead.	FDA H-0511-2026	Food	High	Feb 25, 2026 Recall: Nov 21, 2025	Details
Frozen Cooked Medium Shrimp Peeled & Deveined, Tail Off-White Shrimp; 1 lbs retail plastic bag. UPC: 041220333035 Product manufactured under insanitary conditions whereby it may have been contaminated with Cesium-137 (Cs-137)	FDA H-0516-2026	Food	High	Feb 25, 2026 Recall: Feb 9, 2026	Details
The Tuna Salad product container is mislabeled with a Chicken Salad lid, which states: Molly Kitchen's Chicken Salad, 789953, NET WT. 5 LB (2.26 kg) per plastic tub. UPC 7 5810830149 8. Distributed by US Foods, Inc. Rosemont, IL 60018. The lid declares Contains: Eggs, Milk, Wheat. The immediate 5-lb tub has no side labeling (besides the lid). The master cardboard case label is correct and states: Molly Kitchen's Tuna Salad, (item #) 794599, 2/5 LB tubs per case, Net Wt. 10 LB (4.53 kg). UPC 075810876447. Distributed by US Foods, Inc. Rosemont, IL 60018. Contains: Egg, Wheat, Fish (Tuna). Undeclared fish allergen (tuna). Tuna Salad was mislabeled as Chicken Salad.	FDA H-0517-2026	Food	High	Feb 25, 2026 Recall: Jan 30, 2026	Details
Pure Factors Professional Nighttime Sleep Formula and Pure Formulas Sleep Reset, Net Wt., 1 fl oz (30 ml) liquid dietary supplement, Glass bottle with dropper cap. (Individual 1 fl oz bottles (not sold in case lots) Label declares bovine colostrum but does not declare milk allergen.	FDA H-0537-2026	Food	High	Feb 25, 2026 Recall: Feb 3, 2026	Details
Why Not Natural Moringa Capsules 120 capsule bottle marked with lot # A25G051 on the bottom and with an expiration date of 07/2028 stamped on the bottom. Potential to be contaminated with Salmonella	FDA H-0510-2026	Food	High	Feb 25, 2026 Recall: Jan 28, 2026	Details
Aluminum Kadai with Metal Handles Size 5. A-Cook MADE IN INDIA SIZE 5 Sticker label: $$24.99+TX Potential contamination with leachable lead.	FDA H-0513-2026	Food	High	Feb 25, 2026 Recall: Nov 21, 2025	Details
Brass Pital Pot 4-quart. Sticker label: BRASS HAMMERED HANDI NO 3 UPC 7 023672 414398 US $ 74.99 Sticker label: IKM INDIAN KITCHEN MART Potential contamination with leachable lead.	FDA H-0514-2026	Food	High	Feb 25, 2026 Recall: Nov 21, 2025	Details
Missing Aim Markings on Headlight Assembly/FMVSS 108 Toyota Motor Engineering & Manufacturing (Toyota) is recalling certain 2026 Corolla vehicles. The front headlights may have missing headlight aim markings, which can result in improperly aimed headlights during service. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 108, "Lamps, Reflective Devices, and Associated Equipment." Incorrectly aimed headlights can reduce driver visibility or create a glare for oncoming traffic, increasing the risk of a crash.	NHTSA 26V110000	Vehicle	High	Feb 25, 2026 Recall: Feb 25, 2026	Details

Showing 3,926 - 3,950 of 4,622 product recalls

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Product Recalls Today

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