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.

27826–27850 of 50462

  • HighFDA (Devices)·Z-2954-2018·2018-09-05

    GE Carestation Anesthesia Systems Recalled for Gas Switch Defect

    GE Medical Systems is recalling 310 anesthesia systems worldwide because a gas switch may unexpectedly change position, potentially causing hypoxia.

    Product
    GE Carestation 620/650/650c, A1 and A2 (non-US distribution) anesthesia systems
    Category
    Medical Device
    Distribution
    0 states
  • HighUSDA FSIS·077-2018·2018-09-05

    New York Style Sausage Co. Recalls Raw Chorizo for Undeclared Sesame

    New York Style Sausage Co. is recalling raw chorizo sausage because it contains undeclared sesame seed. No adverse reactions have been reported.

    Product
    NEW YORK STYLE SAUSAGE CO. — New York Style Sausage Co. Recalls Raw Chorizo Sausage Products due to Misbranding and an Undeclared Ingredient
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1911-2018·2018-09-05

    Howard Calcagno Farms Recalls Collards Due to Cyclospora Contamination Risk

    Howard Calcagno Farms is recalling collards shipped in cardboard boxes labeled with the firm's name in Aurora, Oregon, due to a potential for contamination with Cyclospora cayetanensis.

    Product
    Collards were shipped in card board boxes that are labeled with the firm name "Howard Calcagno, Aurora, OR 97002".
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-2940-2018·2018-09-05

    MedComp Recalls Soft-Line Duo-Flow Catheters Due to Suture Wing Cracking

    Medical Components, Inc. is recalling Soft-Line Duo-Flow catheters because suture wings may crack or break, posing a risk of catheter dislocation, bleeding, or air emboli.

    Product
    SOFT-LINE DUO-FLOW DOUBLE LUMEN CATHETER/CATHETER SET; T94C T94M T96M T98M
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2938-2018·2018-09-05

    MedComp Duo-Flow Double Lumen Catheters Recalled for Suture Wing Cracking

    Medical Components, Inc. is recalling Duo-Flow Double Lumen Catheters because suture wings may crack or break, posing risks of catheter dislocation, bleeding, and air emboli.

    Product
    Duo-Flow Double Lumen Catheter Only/Catheter Set; T114C T114M T116C T116M T116ME T118C T118M T118ME T119M
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2928-2018·2018-09-05

    Siemens RAPIDPoint 500 Blood Gas Analyzer Recalled for Hydroxocobalamin Interference

    Siemens recalls RAPIDPoint 500 Blood Gas Analyzers because Hydroxocobalamin may interfere with test results, potentially leading to incorrect medical assessments.

    Product
    RAPIDPoint 500 Blood Gas Analyzer; 10492730, 1069855, 10696857, 10697306 Device is point-of-care system for comprehensive lab-quality testing to patient's bedside. Test menu includes blood gas, electrolytes, glucose, lactate, neonatal total bilirubin and full CO-oximetry…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2933-2018·2018-09-05

    MedComp Recalls Double Lumen CRRT Catheter Sets Due to Suture Wing Cracking

    Medical Components, Inc dba MedComp is recalling specific hemodialysis catheter insertion kits because the suture wings may crack or break, posing a risk of patient injury.

    Product
    Double Lumen CRRT/ABP Catheter Set; Hemodialysis catheter insertion kits, DL 11/15 DL 11/20 DL 9/15
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1855-2018·2018-09-05

    Morgan Foods Recalls Tomato Condensed Soup Due to Undeclared Allergens

    Morgan Foods is recalling 6,168 cans of Tomato Condensed Soup because the product contains cream of mushroom soup with undeclared milk and soy.

    Product
    Tomato Condensed Soup, 26 oz (1 LB 10 OZ) 737 g, 307 x 512 Can, Family Size, 12 cans per tray, shelf stable
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1924-2018·2018-09-05

    Howard Calcagno Farms Recalls Green Chard Due to Cyclospora Contamination Risk

    Howard Calcagno Farms is recalling green chard from Oregon due to a potential contamination with Cyclospora cayetanensis.

    Product
    Green Chard was shipped in card board boxes that are labeled with the firm name "Howard Calcagno, Aurora, OR 97002".
    Category
    Food
    Distribution
    1 state
  • HighCPSC·18765·2018-09-05

    Polaris Recalls 2018 Ranger Recreational Off-Highway Vehicles Due to Crash Hazard

    Polaris is recalling about 1,000 model year 2018 Ranger 500, 570, EV, and EV LI-ION vehicles because front lower control arms can separate, posing a crash hazard.

    Product
    Model year 2018 Polaris Ranger 500, Ranger 570, Ranger EV, and Ranger EV LI-ION recreational off-highway vehicles (ROVs)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1915-2018·2018-09-05

    Howard Calcagno Farms Recalls Green Leaf Lettuce Due to Cyclospora Risk

    Howard Calcagno Farms is recalling Green Leaf Lettuce shipped in Oregon due to potential contamination with Cyclospora cayetanensis.

    Product
    Green Leaf Lettuce was shipped in card board boxes that are labeled with the firm name "Howard Calcagno, Aurora, OR 97002".
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1857-2018·2018-09-05

    Tipu's Chai Sweetened Masala Chai Recalled for Undeclared Milk

    Tipu's Chai is recalling Sweetened Masala Chai boxes because the packaging fails to declare milk, which is present in the single-serve sachets inside.

    Product
    Tipu's Chai - Sweetened Masala Chai, Net wt.7.5 oz. per box. UPC #: 7 19196 20035 3. Each box contains five single serve sachet packets of Chai Tea Latte. Single serve sachet Chai Tea Latte packets, net wt. 1.1 oz per packet. UPC 7 19196 20073 5. The LABEL of Sweetened…
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1901-2018·2018-09-05

    Hostess Brownies Cookies 'n Crème Recalled for Missing Egg Allergen Labeling

    Hostess Brands is recalling specific lots of Brownies Cookies 'n Crème because the packaging fails to declare egg in the 'Contains' statement, despite egg being an ingredient.

    Product
    Hostess Brownies Cookies 'n Cr¿me packaged in the following ways: 1) 6 Brownies individually wrapped packaged in a cardboard box Net Wt. 8.68 OZ (246 g) UPC 888109113575; 2) 2 Brownies packaged in a cardboard box Net Wt. 2.89 OZ (82 g) UPC 888109012021
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2930-2018·2018-09-05

    Siemens RAPIDLab 1265 Blood Gas Analyzer Recalled for Hydroxocobalamin Interference

    Siemens is recalling 2,357 RAPIDLab 1265 Blood Gas Analyzers because Hydroxocobalamin may interfere with test results, potentially leading to incorrect medical assessments.

    Product
    RAPIDLab 1265 Blood Gas Analyzer; 110321852, 10470366, 10491395 Device is point-of-care system for comprehensive lab-quality testing to patient's bedside. Test menu includes blood gas, electrolytes, glucose, lactate, neonatal total bilirubin and full CO-oximetry including…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1128-2018·2018-09-05

    Baxter Recalls 0.9% Sodium Chloride Injection Due to CGMP Deviations

    Baxter Healthcare is recalling 33,600 bags of 0.9% Sodium Chloride Injection USP due to Current Good Manufacturing Practice (CGMP) deviations. The product was distributed only in Texas and Mississippi.

    Product
    SODIUM CHLORIDE — SODIUM CHLORIDE (SODIUM CHLORIDE)
    Category
    Drug
    Distribution
    2 states
  • HighFDA (Devices)·Z-2950-2018·2018-09-05

    Haemonetics OrthoPAT System-Integrated Set Recalled Due to Missing Cannula

    Haemonetics is recalling OrthoPAT System-Integrated Sets because missing cannulas prevent blood from emptying, making the collected blood unusable.

    Product
    Haemonetics OrthoPAT System-Integrated Set. Product Code: 1150H-00 OrthoPAT orthopedic perioperative autotransfusion system indicated for use to salvage RBCs from blood lost intraoperatively and postoperatively during surgical procedures
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1922-2018·2018-09-05

    Howard Calcagno Farms Recalls Beets for Potential Cyclospora Contamination

    Howard Calcagno Farms is recalling beets shipped in cardboard boxes due to a potential for contamination with Cyclospora cayetanensis.

    Product
    Beet was shipped in card board boxes that are labeled with the firm name "Howard Calcagno, Aurora, OR 97002".
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-2925-2018·2018-09-05

    Stryker Mako Vizadisc Hip Procedure Tracking Kit Recall for Detection Failure

    Mako Surgical Corporation is recalling specific lots of the Stryker Mako Vizadisc Hip Procedure Tracking Kit because damaged reflective material may prevent camera detection.

    Product
    Stryker Mako Vizadisc Hip Procedure Tracking Kit
    Category
    Medical Device
    Distribution
    35 states
  • HighFDA (Food)·F-1929-2018·2018-09-05

    Premo Turkey & Cheese Wedge Sandwiches Recalled for Listeria Risk

    Lipari Foods is recalling Premo Turkey & Cheese Wedge sandwiches due to potential Listeria monocytogenes contamination.

    Product
    Premo Brand Turkey & Cheese Wedge sandwiches 5 OZ retail UPC 612510002018 Plastic triangle sandwich wedge container with plastic film. Refrigerated. 4, 5 OZ retail units per wholesale case.
    Category
    Food
    Distribution
    11 states
  • HighFDA (Devices)·Z-2946-2018·2018-09-05

    Civco Needle Guide Recall Due to Missing or Inadequate Adhesive

    Civco Medical Instruments is recalling 107 units of CIVCO Needle Guides because the assembly may lack sufficient adhesive to hold the cannula in place.

    Product
    CIVCO Needle Guide, REF 676-144, QTY 24, STERILE EO
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2931-2018·2018-09-05

    CSL Behring Recalls N Latex CDT Kits Due to Measurement Bias

    CSL Behring is recalling N Latex CDT Kits because they may produce inaccurate results that are approximately 15% lower than expected.

    Product
    N Latex CDT Kit
    Category
    Medical Device
    Distribution
    5 states
  • HighFDA (Devices)·Z-2927-2018·2018-09-05

    Siemens RAPIDPoint 405 Blood Gas Analyzer Recalled for Interference

    Siemens is recalling RAPIDPoint 405 Blood Gas Analyzers because Hydroxocobalamin may interfere with test results, potentially leading to incorrect medical assessments.

    Product
    RAPIDPoint 405 Blood Gas Analyzer; 10282093, 10310464, 10314817, 10317193, 10318999, 10320055, 10321238, 10322347, 10328278, 10328302, 10336784 Device is point-of-care system for comprehensive lab-quality testing to patient's bedside. Test menu includes blood gas…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2932-2018·2018-09-05

    MedComp Recalls Hemodialysis Catheter Kits Due to Suture Wing Cracking Risk

    Medical Components, Inc. is recalling specific hemodialysis catheter insertion kits because suture wings may crack or break, posing a risk of patient injury.

    Product
    Duo-Flow XTP Straight Full Set; Hemodialysis catheter insertion kits, AAC02106 AAC02107 AAC02108
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1918-2018·2018-09-05

    Howard Calcagno Farms Recalls Bok Choy Due to Cyclospora Contamination Risk

    Howard Calcagno Farms is recalling 30-pound boxes of Bok Choy distributed in Oregon due to a potential for contamination with Cyclospora cayetanensis.

    Product
    Bok Choy was shipped in card board boxes that are labeled with the firm name "Howard Calcagno, Aurora, OR 97002".
    Category
    Food
    Distribution
    1 state