Latest Product Recalls Today

Recent Product Recall Alerts List

Showing 276 - 300 of 4,975 matching product recalls.

Product Recall	Source	Type	Risk	Date	Action
Deano's Pasta; Pear and Pecorino Triangoli Ravioli, 1lb.; Ingredients: Dough: Semolina (Wheat, Niacin, Thiamine, Mononitrate, Riboflavin, Folic Acid), Water, Fresh Eggs, Salt. Filling: Pears, Ricotta (Whey, Cream, Milk), Pecorino Cheese (Milk, Cultures, Salt, Enzymes), Breadcrumbs (Wheat Flour, Cane Sugar, Yeast, Salt), Brandy, Dark Brown Sugar, Salt, Black Pepper.; CONTAINS: WHEAT, MILK, EGG ingredients; MAY CONTAIN OTHER ALLERGENS; KEEP FROZEN Undeclared Lobster	FDA H-0092-2027	Food	High	Oct 21, 2026 Recall: Sep 23, 2026	Details
Holsum Spinach Flour Tortillas Large, 8 count (20 oz.) UPC: 810023430629 Undeclared colors (FD&C Blue No. 1 and FD&C Yellow No. 5)	FDA H-0089-2027	Food	High	Oct 21, 2026 Recall: Sep 28, 2026	Details
Stewarts Shops Vanilla chocolate Strawberry Ice Cream 1/2 gallon (1.89 L), UPC: 0 82086 44377 3 Foreign object: May contain pieces of metal	FDA H-0093-2027	Food	High	Oct 21, 2026 Recall: Oct 2, 2026	Details
Made From Plants; Daring; Plant Steak Bites; Ready in 4 Mins Microwaveable Pouch; UPC: 86001124319 defective packaging; packaging can rupture/explode during cooking.	FDA H-0091-2027	Food	High	Oct 21, 2026 Recall: Sep 24, 2026	Details
Pur Aqua Sparkling Frost Cherry Limeade 17 oz., UPC: 4099100167023 May contain undeclared aspartame.	FDA H-0095-2027	Food	High	Oct 21, 2026 Recall: Oct 7, 2026	Details
J. HIGGS Loaded Bacon & Cheddar Potato Chips, NET WT 7.75 OZ (219.7g) bag, UPC 051933316454. Sold as 13 (7.75oz) bags per case. Undeclared soy.	FDA H-0090-2027	Food	High	Oct 21, 2026 Recall: Sep 15, 2026	Details
Stewarts Shops Vanilla Heavenly Medley 1/2 Gallon (1.89 L), UPC Codes: 0 82086 44371 1 Foreign object: May contain pieces of metal	FDA H-0094-2027	Food	High	Oct 21, 2026 Recall: Oct 2, 2026	Details
RAPICIDE PA Part A High-Level Disinfectant, Model/Catalog Number: ML020116 If the vented cap becomes blocked, gas may accumulate and the bottle may swell due to increased internal pressure. In some cases, excess vapor or liquid chemistry may escape from the bottle when the cap is twisted during opening, which could result in user exposure if required personal protective equipment (PPE) is not properly used. Such exposure may result in injury to the user or others in close proximity.	FDA Z-0155-2027	Medical Device	High	Oct 21, 2026 Recall: Sep 21, 2026	Details
NeuroStar Advanced Therapy System. Contains the NeuroStar HP Coil Assembly Part Number 81-01000-200. Affects the below NeuroStar Advanced Therapy Systems: 1. NeuroStar 2.0 US; Part Number: 81-01315-000. 2. NeuroStar 3.0 US; Part Number: 81-02315-000. 3. NeuroStar 2.X to 3.2 Upgrade Kit; Part Number: 81-25000-100. 4. NeuroStar Upgrade Kit 3.0 US; Part Number: 81-35000-000. 5. NeuroStar Mobile Console 3.6, 120V, US; Part Number: 81-03315-000. 6. NeuroStar Mobile Console 3.7, 120V, US; Part Number: 81-04315-000. 7. NeuroStar Mobile Console 3.8, 120V, US; Part Number: 81-05315-000. Cables are not in conformance with the product specifications required in the production of the HP Coil Assembly.	FDA Z-0142-2027	Medical Device	High	Oct 21, 2026 Recall: Aug 24, 2026	Details
Medline surgical convenience kits labeled as: 1) EAR, Medline product number/SKU DYNJ909020B; 2) EAR, Medline product number/SKU DYNJ909020A; 3) CAROTID PACK, Medline product number/SKU DYNJ42922C; 4) EAR, Medline product number/SKU DYNJ909020; 5) FEM CAROTID PACK, Medline product number/SKU DYNJ65706; 6) CAROTID CDS-LF, Medline product number/SKU CDS983139B. Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to leaking or breaking during use.	FDA Z-0173-2027	Medical Device	High	Oct 21, 2026 Recall: Sep 2, 2026	Details
NaviFlex LW Pusher; Advx Panc. Stent 4/5F; Material Number (UPN): M00535030; Device was incorrectly manufactured with a guidewire exit port (referred to in the IFU as the RX port), which is not a design feature associated with this device configuration.	FDA Z-0143-2027	Medical Device	High	Oct 21, 2026 Recall: Sep 10, 2026	Details
Generic Name: FilmArray¿ Pneumonia Panel Generic Name: FilmArray¿ Pneumonia Panel Model/Catalog Number: RFIT-ASY-0144 (30 pack), RFIT-ASY-0145 (6 pack), FLM1-ASY-0150 (Verification Kits). Verification kit lots (FLM1-ASY-0150) are a sales configuration that consume kits from panel lots (RFIT-ASY-0144). Software Version: N/A Product Description: Multiple-type respiratory pathogen nucleic acid IVD, kit, nucleic acid technique (NAT) Component: N/A Due to potential contaiminated of spefic lots of pneumonia and joint infection panels that could result in false positive results	FDA Z-0148-2027	Medical Device	High	Oct 21, 2026 Recall: Aug 12, 2026	Details
TS Misc. Instruments Tray, Triathlon. Catalog Number: 6543-6-519. Reprocessing instructions provided in LSTPI-B specify a sterilization dry time of 30 minutes for the trays sterilized in blue wrap. When blue wrap is used, the 30-minute dry time may lead to a small amount of residual moisture remaining after sterilization.	FDA Z-0167-2027	Medical Device	High	Oct 21, 2026 Recall: Sep 16, 2026	Details
BD Phoenix Panel NMIC-306. Catalog Number: 449292. Potential for quality control failures with Klebsiella pneumoniae ATCC BAA-1705 when using the CPO Ambler classification feature.	FDA Z-0140-2027	Medical Device	High	Oct 21, 2026 Recall: Aug 13, 2026	Details
JenaValve Trilogy Delivery Catheter, Size 23MM REF: TRILOGY-DC-S Delivery Catheter may have sleeve liner separation that results in difficulty or inability to deploy heart valve device.	FDA Z-0134-2027	Medical Device	High	Oct 21, 2026 Recall: Jul 31, 2026	Details
Convenience Kits containing CONMED AirSeal Access Ports ADVANCE LAPAROSCOPIC DYNJ911135 LAP CHOLE DYNJ911660 LAP NISSEN DYNJ911560 UROLOGY LAPAROSCOPIC - 51638 DYNJ908720A Kits contain CONMED AirSeal Access Ports. The ports were recalled by manufacturer due to potential for erroneous overpressure alerts and system venting during use, which may result in delays or ending procedures.	FDA Z-0180-2027	Medical Device	High	Oct 21, 2026 Recall: Aug 31, 2026	Details
Medline surgical convenience kits labeled as: CABG AUXILIARY PACK, Medline Product Number/SKU DYNJ44925D Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to leaking or breaking during use.	FDA Z-0168-2027	Medical Device	High	Oct 21, 2026 Recall: Sep 2, 2026	Details
Scout MD, REF MDS05A-01, MDS05C-01, MDS10C-01 Contents: (1) Scout MD Delivery System, Standard for use with the SCOUT MD Surgical Guidance System, Rx Only, Sterile-EO The implantable clip may experience difficulties deploying, which could prevent the reflector from functioning as intended during use.	FDA Z-0187-2027	Medical Device	High	Oct 21, 2026 Recall: Aug 27, 2026	Details
Vinyl Instrument Guards, labeled as: 1) VENTED INSTRUMENT GUARD 1/16 X 3/4H - WHITE, Model Number 09-1-011; 2) WHITE VENTED INSTRUMENT GUARD 1/16 X 3/4, Model Number 09-1-011; 3) VENTED INSTRUMENT GUARD 5/64 X 3/4 - BLUE, Model Number 09-1-012; 4) BLUE VENTED INSTRUMENT GUARD 5/64 X 3/4, Model Number 09-1-012; 5) VENTED INSTRUMENT GUARD 7/64 X 3/4 - GREEN, Model Number 09-1-013; 6) GREEN VENTED INSTRUMENT GUARD 7/64 X 3/4, Model Number 09-1-013; 7) VENTED INSTRUMENT GUARD 1/8 X 1 - RED, Model Number 09-1-014; 8) RED VENTED INSTRUMENT GUARD 1/8 X 1, Model Number 09-1-014; 9) VENTED INSTRUMENT G Labeling not compliant with 21 CFR 801 and steam sterilization IFU has been updated.	FDA Z-0188-2027	Medical Device	High	Oct 21, 2026 Recall: Sep 7, 2026	Details
BD Phoenix Panel NMIC-312. Catalog Number: 449082. Potential for quality control failures with Klebsiella pneumoniae ATCC BAA-1705 when using the CPO Ambler classification feature.	FDA Z-0139-2027	Medical Device	High	Oct 21, 2026 Recall: Aug 13, 2026	Details
Convenience Kits containing CONMED AirSeal Access Ports HERNANDEZ DAVINCI ACC BUNDLE M DYNJ911258 KIT ROBOTICS UROLOGY PROSTATE DYKMBNDL116I ROBOTIC CHEST DYNJ910997 DYNJ910997A RR-DAVINCI PROSTATE ACCESSORY DYNJ63392D UROLOGY LAPAROSCOPIC - 51638 DYNJ908720B UROLOGY ROBOT ADD ON PACK DYNJ85189 Kits contain CONMED AirSeal Access Ports. The ports were recalled by manufacturer due to potential for erroneous overpressure alerts and system venting during use, which may result in delays or ending procedures.	FDA Z-0181-2027	Medical Device	High	Oct 21, 2026 Recall: Aug 31, 2026	Details
Curaplex Capnography EtCO2/O2 Oral/Nasal Cannula Multipack (10 pk), Item Number 670272-KIT Affected kits were assembled with pediatric nasal cannula instead of the intended adult nasal cannula.	FDA Z-0144-2027	Medical Device	High	Oct 21, 2026 Recall: Jun 12, 2026	Details
Convenience Kits containing CONMED AirSeal Access Ports GENERAL DAVINCI DYNJG901004C LAP CHOLE DYNJ88071 ROBOTIC PACK DYNJ50474F Kits contain CONMED AirSeal Access Ports. The ports were recalled by manufacturer due to potential for erroneous overpressure alerts and system venting during use, which may result in delays or ending procedures.	FDA Z-0182-2027	Medical Device	High	Oct 21, 2026 Recall: Aug 31, 2026	Details
1) Product Name AUD OPEN HEART PACK, Medline Kit Number/SKU DYNJ22052I; 2) Product Name AV SHUNT PACK-MARYVIEW, Medline Kit Number/SKU DYNJ24528N; 3) Product Name AV SHUNT PACK-MARYVIEW, Medline Kit Number/SKU DYNJ24528O; 4) Product Name AV SHUNT PACK-MARYVIEW, Medline Kit Number/SKU DYNJ24528P; 5) Product Name CATH LAB ENDO AAA, Medline Kit Number/SKU DYNJ35312J; 6) Product Name CATH LAB ENDO AAA, Medline Kit Number/SKU DYNJ35312K; 7) Product Name OPEN HEART PACK, Medline Kit Number/SKU DYNJ43937; 8) Product Name OPEN HEART PACK, Medline Kit Number/SKU DYNJ80549D; 9) Product Name CV PART 1 AN Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to leaking or breaking during use.	FDA Z-0169-2027	Medical Device	High	Oct 21, 2026 Recall: Sep 2, 2026	Details
Generic Name: FilmArray¿ Pneumonia Panel plus Generic Name: FilmArray¿ Pneumonia Panel plus Model/Catalog Number: RFIT-ASY-0143 (30 Kit), RFIT-ASY-0142 (6 Kit) Software Version: N/A Product Description: Multiple-type respiratory pathogen nucleic acid IVD, kit, nucleic acid technique (NAT) Component: N/A Due to potential contaiminated of spefic lots of pneumonia and joint infection panels that could result in false positive results	FDA Z-0149-2027	Medical Device	High	Oct 21, 2026 Recall: Aug 12, 2026	Details

Showing 276 - 300 of 4,975 product recalls

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Product Recalls Today

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