The Recall Desk

Severity 3 of 5

High recalls

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

What “high” means here

Severity 3 (High) recalls have a known hazard but no confirmed illness, injury, or property damage in the source text. The risk is theoretical-but-real: a pathogen pre-emptively pulled from shelves before anyone got sick, an allergen mislabeling on an uncommon allergen, a precautionary correction on a device that hasn't yet malfunctioned in the field. Most allergen recalls land here, as do most preventive food recalls based on routine sampling. You should still stop using the product, but you don't need to panic.

The full rubric is on the methodology page. Severity is computed deterministically from the agency’s own classification plus the source text — no editorial vibes.

27201–27225 of 50462

  • HighFDA (Food)·F-0209-2019·2018-10-31

    McCain Recalls Fire-Roasted Red Pepper Strips Due to Listeria and Salmonella

    McCain Foods USA is recalling Fire-Roasted Red Pepper Julienne Strips because finished product was released after presumptive positive tests for Listeria monocytogenes and Salmonella without confirmation.

    Product
    Fire-Roasted Red Pepper Julienne Strips: Sold in 2 lb. and 25 lb. packages. Brand Name: Jon-Lin¿ NatureSmart¿; Jon-Lin¿
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-0200-2019·2018-10-31

    Smith+Nephew Legion AP Femoral Cutting Block Recalled for Oversized Spring

    Smith & Nephew is recalling one lot of Legion AP femoral cutting blocks, size 6, because they were manufactured with an oversized spring.

    Product
    Smith+Nephew Orthopaedic Division LEGION A/P FEMORAL CUTTING BLOCK, SIZE 6 REF 71434411, QTY: (1) The LEGION AP Femoral Cutting Block is a reusable surgical instrument used to make bone cuts on the distal femur to prepare the bone to receive a LEGION femoral implant.
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Devices)·Z-0265-2019·2018-10-31

    Custom Healthcare Systems Recalls Surgical Gowns Due to Sterility Compromise

    Custom Healthcare Systems is recalling 89 units of surgical gowns and convenience kits because incorrect sealing specifications compromised product sterility.

    Product
    CHS Custom Convenience Kit: 1231-110XL SURGICAL GOWN, NRF W. HAND TOWEL 1231-080XL GOWN, SURGICAL XXL 1231-150XL GOWN, SURGICAL XXL
    Category
    Medical Device
    Distribution
    9 states
  • HighFDA (Food)·F-0204-2019·2018-10-31

    McCain Foods Recalls Fire Roasted Diced Red Peppers Due to Listeria and Salmonella

    McCain Foods USA is recalling Fire Roasted Diced Red Peppers because finished product was released after presumptive positive tests for Listeria monocytogenes and Salmonella without confirmation.

    Product
    Fire Roasted 1/2" Diced Red Peppers; Sold in 2 lb. and 25 lb. containers Brand name: Jon-Lin¿
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-0201-2019·2018-10-31

    GE Healthcare Recalls 3.0T MR750 MRI Scanners Due to Coil Overheating Risk

    GE Medical Systems is recalling 356 Discovery 3.0T MR750 MRI scanners because a specific coil can overheat in Mode 2, posing a risk of serious patient thermal injury.

    Product
    GE Healthcare, Discovery 3.0T MR750, 5148810-2, 5373011-2, 5499460-2.
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Food)·F-0239-2019·2018-10-31

    McCain Foods Recalls Sautéed Onion Strips Due to Listeria and Salmonella Testing Issues

    McCain Foods USA is recalling Sautéed Julienne Onion Strips because finished product was released after presumptive positive tests for Listeria monocytogenes and Salmonella without confirmation.

    Product
    Saut¿ed Julienne Onion Strips With Canola Caramel; Sold in 20 lb. containers. Brand Name: Jon-Lin¿
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0208-2019·2018-10-31

    McCain Foods Recalls Caramelized Onion Strips Due to Listeria and Salmonella

    McCain Foods USA is recalling Caramelized Onion Strips because finished product was released after presumptive positive tests for Listeria monocytogenes and Salmonella without confirmation.

    Product
    Caramelized Onion Strips: Sold in 2 lb. and 25 lb. packages. Brand Name: Jon-Lin¿ NatureSmart¿; Jon-Lin¿
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-0209-2019·2018-10-31

    Siemens APTIO Input/Output Modules Recalled for Missing Pacemaker Warning Label

    Siemens Healthcare Diagnostics is recalling 441 APTIO Input/Output Modules because they may have been shipped without a warning label regarding potential interference with pacemaker functionality.

    Product
    APTIO INPUT/OUTPUT MODULE
    Category
    Medical Device
    Distribution
    38 states
  • HighFDA (Food)·F-0228-2019·2018-10-31

    Jalapeno Poblano Onion Blend Recalled Due to Presumptive Listeria and Salmonella Test Results

    McCain Foods USA recalled its Jalapeno Poblano Onion Blend because internal testing found presumptive positive results for Listeria monocytogenes and Salmonella, though no confirmed illnesses were reported.

    Product
    Jalapeno Poblano Onion Blend; Sold in 2 lb. and 25 lb. containers. Brand Name:Jon-Lin¿
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-0255-2019·2018-10-31

    Custom Healthcare Systems Recalls Sterility-Compromised Connector Packs

    Custom Healthcare Systems is recalling 150 units of CHS Custom Convenience Kit-CONNECTOR PACK due to incorrect sealing specifications that compromised product sterility.

    Product
    CHS Custom Convenience Kit-CONNECTOR PACK Product Number:D36-7520
    Category
    Medical Device
    Distribution
    9 states
  • HighFDA (Food)·F-0213-2019·2018-10-31

    McCain Foods Recalls Fire Roasted Zucchini Due to Listeria and Salmonella

    McCain Foods USA is recalling Fire Roasted Half Moon Green Zucchini because finished product was released after presumptive positive tests for Listeria monocytogenes and Salmonella without confirmation.

    Product
    Fire Roasted Half Moon Green Zucchini : Sold in 25 lb. and 1200 lb. packaging. Brand Name: Jon-Lin¿
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-0280-2019·2018-10-31

    Medtronic Recalls O-arm 1000 2nd Edition Imaging Systems Due to Software Anomalies

    Medtronic is recalling 596 O-arm 1000 2nd Edition Imaging Systems worldwide due to reported software anomalies affecting startup, motion control, and image acquisition.

    Product
    O-arm 1000 2nd Edition Imaging System, OARM ASSY Bl70000027GERR SYS PRODUCT REFURB, Model Number Bl70000027GERR Product Usage: The O-arm Imaging System is a mobile x-ray system designed for 2D fluoroscopic and 3D imaging and is intended to be used where a physician benefits…
    Category
    Medical Device
    Distribution
    45 states
  • HighFDA (Devices)·Z-0263-2019·2018-10-31

    Custom Healthcare Systems Recalls Convenience Kits Due to Sterility Compromise

    Custom Healthcare Systems is recalling 60 units of CHS Custom Convenience Kits because incorrect sealing specifications compromised product sterility.

    Product
    CHS Custom Convenience Kit-TUBING W. CONNECTOR Product Number:UNC-10884
    Category
    Medical Device
    Distribution
    9 states
  • HighFDA (Food)·F-0226-2019·2018-10-31

    McCain Recalls Fire-Roasted Bell Peppers and Onions Due to Listeria and Salmonella

    McCain Foods USA is recalling Trader Joe's Fire-Roasted Bell Peppers and Onions because products were released after presumptive positive tests for Listeria monocytogenes and Salmonella without confirmation.

    Product
    Fire-Roasted Bell Peppers and Onions Sold in 14 oz. package. Brand Name:Trader Joe's none
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0322-2019·2018-10-31

    McCain Recalls Fire-Roasted Green Pepper Strips Due to Listeria and Salmonella

    McCain Foods USA is recalling 7,219 cases of Fire-Roasted Home-Style Green Pepper Strips because finished product was released after presumptive positive tests for Listeria monocytogenes and Salmonella.

    Product
    Fire-Roasted Home-Style Green Pepper Strips;: Sold in 20 lb. containers. Brand Name: Jon-Lin¿
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-0277-2019·2018-10-31

    Medtronic Recalls O-arm 1000 2nd Edition Imaging Systems for Software Anomalies

    Medtronic Navigation is recalling 596 O-arm 1000 2nd Edition Imaging Systems worldwide due to reported software anomalies affecting startup, communication, and image acquisition.

    Product
    O-arm 1000 2nd Edition Imaging System, BASE OARM Bl70000027230 SYSTEM 230V, Model Number Bl7000002 7230 Product Usage: The O-arm Imaging System is a mobile x-ray system designed for 2D fluoroscopic and 3D imaging and is intended to be used where a physician benefits from 2D…
    Category
    Medical Device
    Distribution
    45 states
  • HighFDA (Food)·F-0227-2019·2018-10-31

    McCain Recalls Sautéed Organic Onion Strips Due to Listeria and Salmonella

    McCain Foods USA is recalling Sautéed Organic Onion Strips because finished product was released after presumptive positive tests for Listeria monocytogenes and Salmonella without confirmation.

    Product
    Saut¿ed Organic Onion Strips; Sold in 25 lb. containers. Brand Name:Jon-Lin¿ NatureSmart¿
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0329-2019·2018-10-31

    McCain Recalls Fire-Roasted Organic Corn Due to Listeria and Salmonella Testing Issues

    McCain Foods USA is recalling Fire-Roasted Organic Super Sweet Corn because finished product was released after presumptive positive tests for Listeria monocytogenes and Salmonella without confirmation.

    Product
    FIRE-ROASTED ORGANIC SUPER SWEET CORN; Sold in 1500 lb. containers. Brand Name: Jon-Lin¿
    Category
    Food
    Distribution
    0 states
  • HighNHTSA·18V768000·2018-10-31

    Forest River Recalls Motorhomes Due to Windshield Shade Visibility Hazard

    Forest River is recalling specific 2017-2019 motorhomes because the driver's windshield roller shade may unroll unexpectedly, blocking visibility and increasing crash risk.

    Product
    FOREST RIVER — FOREST RIVER BERKSHIRE, CHARLESTON, GEORGETOWN, FR3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0221-2019·2018-10-31

    McCain Foods Recalls Fire Roasted Diced Red Peppers Due to Pathogen Testing Failures

    McCain Foods USA is recalling Fire Roasted 1/4" Diced Red Peppers because finished product was released after presumptive positive tests for Listeria monocytogenes and Salmonella without confirmation.

    Product
    Fire Roasted 1/4" Diced Red Peppers: Sold in 25 lb. Brand Name: Jon-Lin¿
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-0266-2019·2018-10-31

    Custom Healthcare Systems Recalls Non-Sterile Convenience Gowns

    Custom Healthcare Systems is recalling 72,832 units of convenience gowns because they were sealed with incorrect specifications, compromising sterility.

    Product
    CHS Custom Convenience (1) 1231-150L GOWN, RAGLAN, LG, NONREINF (2) 1231-150XL GOWN, RAGLAN, XL, NONREINF (3) 1231-140XL GOWN, SPECIALTY XL, XLONG
    Category
    Medical Device
    Distribution
    9 states
  • HighFDA (Devices)·Z-0274-2019·2018-10-31

    Medtronic Recalls O-arm 1000 2nd Edition Imaging Systems Due to Software Anomalies

    Medtronic is recalling 596 O-arm 1000 2nd Edition Imaging Systems worldwide due to reported software anomalies affecting startup, communication, and imaging functions.

    Product
    O-arm 1000 2nd Edition Imaging System, BASE OARM Bl70000027100R SYSTEM lOOV RWK, Model Number Bl70000027100R Product Usage: The O-arm Imaging System is a mobile x-ray system designed for 2D fluoroscopic and 3D imaging and is intended to be used where a physician benefits…
    Category
    Medical Device
    Distribution
    45 states