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.

41451–41475 of 50511

  • HighFDA (Devices)·Z-1443-2014·2014-04-16

    Smiths Medical HOTLINE Fluid Warming Set Recall for Injection Port Leaks

    Smiths Medical is recalling HOTLINE Fluid Warming Sets because the injection port septum may leak or become dislodged, potentially causing blood or IV fluid leaks.

    Product
    Smiths Medical HOTLINE¿ Fluid Warming Set L-70. Product Usage: intended for the delivery of warmed blood and intravenous fluids at normothermic temperatures under gravity conditions
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1437-2014·2014-04-16

    DePuy Shoulder Guide Pin Recall Due to Breakage Risk

    DePuy Orthopaedics is recalling 21,675 GLOBAL Anchor Peg Glenoid Plus 2.5mm Breakaway Guide Pins because they may break and be left in patients during surgery.

    Product
    GLOBAL¿ Anchor Peg Glenoid Plus (APG+) 2.5MM Breakaway Guide Pin Part # 2230-00-019, Non-Sterile, DePuy, Johnson & Johnson Product Usage: Usage: The GLOBAL APG+ 2.5mm Guide Pin is a single-use instrument that is used to assist the surgeon in the orientation of the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·14V197000·2014-04-16

    Cummings recalls wheelchair lifts on Ford and Chevrolet vans

    Cummings Mobility is recalling wheelchair lifts on certain Ford and Chevrolet vans because roll stop latches may bend, posing a fall risk.

    Product
    FORD — FORD, CHEVROLET E-350, C5500, G3500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1447-2014·2014-04-16

    Breg Recalls Knee Supports for Missing Latex Warning Labels

    Breg Inc is recalling two knee support models because they contain latex but lack the required caution label.

    Product
    K-Lite Knee 2 Stays with Visco, Model No. 122015. Product Usage: The product is intended to provide flexible knee support.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·14V193000·2014-04-16

    Wheeled Coach Recalls Ambulances Due to Electrical Timer Power Loss

    Wheeled Coach is recalling specific ambulances because an electrical timer may lose power, potentially cutting electricity to the patient area and increasing injury risk.

    Product
    WHEELED COACH — WHEELED COACH AMBULANCE-M2 CHASSIS, T3, T2, T1
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1434-2014·2014-04-16

    Aspen Surgical Recalls Sterile Wound Drainage Kits Due to Sterility Concerns

    Aspen Surgical Products is recalling sterile wound drainage kits because the sterile barrier may be compromised, potentially exposing patients to contamination.

    Product
    7mm Drain Kit Flat Full Perforated with Trocar and 100ml S-Vac Bulb Evacuator, Sterile (10/case) Intended for closed wound suction drainage
    Category
    Medical Device
    Distribution
    35 states
  • HighFDA (Food)·F-1753-2014·2014-04-16

    Keen-Wah Quinoa Clusters Recalled for Undeclared Soy Allergen

    Keen-Wah LLC is recalling i heart keenwah Peanut Butter Cacao All Natural Quinoa Clusters because an anti-stick spray containing soy lecithin was used during manufacture, and soy was not declared on the label.

    Product
    i heart keenwah Peanut Butter Cacao All Natural Quinoa Clusters. UPC 736211884442 - 4 oz 12 units/cs
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1429-2014·2014-04-16

    Aspen Surgical Recalls Sterile Wound Drainage Kits Due to Sterility Concerns

    Aspen Surgical Products is recalling sterile wound drainage kits because the sterile barrier may be compromised, potentially exposing patients to contamination.

    Product
    10mm Drain Kit Flat 3/4 Perforated with 100ml S-Vac Bulb Evacuator, Sterile (10/case) Intended for closed wound suction drainage
    Category
    Medical Device
    Distribution
    35 states
  • HighFDA (Devices)·Z-1430-2014·2014-04-16

    Aspen Surgical Products Recalls Sterile Wound Drainage Kits

    Aspen Surgical Products is recalling sterile wound drainage kits due to a potential compromise of the sterile barrier.

    Product
    7mm Drain Kit Flat Full Perforated with 100ml S-Vac Bulb Evacuator, Sterile (10/case) Intended for closed wound suction drainage
    Category
    Medical Device
    Distribution
    35 states
  • HighFDA (Devices)·Z-1335-2014·2014-04-16

    Intuitive Surgical Recalls 5mm Curved Cannulae for da Vinci System

    Intuitive Surgical is recalling 5,217 5mm Curved Cannulae for the da Vinci Si Surgical System because they may become damaged during use. The recall also includes labeling updates to guide inspection and handling.

    Product
    5X250 MM Curved Cannula, Arm 2 for use with daVinci SI Surgical System, model number IS3000. Intuitive Surgical 1266 Kifer Road Sunnyvale, CA 94086 The Intuitive Surgical da Vinci Single-Site Instruments and Accessories used with the da Vinci Si Surgical System (IS3000)…
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Drugs)·D-1198-2014·2014-04-16

    Terra-Medica Recalls Pleo Not Portable Sips Due to Penicillin Contamination

    Terra-Medica Inc. is recalling specific batches of Pleo Not Portable Sips oral homeopathic medicine due to penicillin cross-contamination.

    Product
    Pleo Not PORTABLE SIPS 7X,10 x 1 mL Cartons, Oral Homeopathic Medicine, OTC Only. Made in Germany, Distributed by: SANUM USA Corp., 1465 Slater Road, Ferndale, WA 98248. Manufactured by: Sanum-Kehlbeck GmbH & Co. KG. NDC: 49807-2310-1. Pleo Not PORTABLE SIPS 7X, 50 x 1 mL…
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1427-2014·2014-04-16

    Aspen Surgical Wound Drainage Kits Recalled for Sterility Concerns

    Aspen Surgical Products is recalling wound drainage kits due to a potential compromise of the sterile barrier, posing a risk of infection.

    Product
    10mm Drain Kit Flat 3/4 Perforated with Trocar and 100ml S-Vac Bulb Evacuator, Sterile (10/case) Intended for closed wound suction drainage
    Category
    Medical Device
    Distribution
    35 states
  • HighFDA (Devices)·Z-1422-2014·2014-04-16

    Aspen Surgical Recalls Sterile Bulb Evacuator Due to Sterility Concerns

    Aspen Surgical Products is recalling sterile bulb evacuators because the sterile barrier may be compromised, potentially increasing infection risk.

    Product
    Saber 100ml Infection Control PVC Bulb Evacuator, Sterile (10/case) Intended to provide manual suction and collection of fluids for closed wound drainage systems
    Category
    Medical Device
    Distribution
    35 states
  • HighFDA (Devices)·Z-1420-2014·2014-04-16

    Aspen Surgical Products Recalls Sterile Wound Drainage Kits

    Aspen Surgical Products is recalling sterile wound drainage kits due to a potential compromise of the sterile barrier.

    Product
    15FR Drain Kit, Flat Full Perforated with Trocar, Saber 100ml Bulb and 3C System, Sterile (10/case) Intended for closed wound suction drainage
    Category
    Medical Device
    Distribution
    35 states
  • HighNHTSA·14V194000·2014-04-16

    Free Spirit Recreational Vehicles Recalled for Trailer Wiring Defect

    Triple E Recreational Vehicles is recalling 2012-2014 Free Spirit models because trailer hazard lights may not work when the RV ignition is off.

    Product
    FREE SPIRIT — FREE SPIRIT FS22SS, FS22, FS22TE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1193-2014·2014-04-16

    Terra-Medica Recalls Pleo Not Capsules Due to Penicillin Cross Contamination

    Terra-Medica Inc. is recalling Pleo Not Capsules 4X because of penicillin cross contamination. The product was distributed in the US, Canada, and the Philippines.

    Product
    Pleo Not CAPSULES 4X, 20 Tablet Cartons, Oral Homeopathic Fever Reducer/ Cough Suppressant/ Decongestant Medicine, OTC Only. Made in Germany, Distributed by: SANUM USA Corp.,1465 Slater Road, Fernadale, WA 98248; Manufactured By: SANUM-Kehlbeck GmbH & Co. KG. NDC: 49807-2303-1.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1423-2014·2014-04-16

    Aspen Surgical Recalls Sterile Wound Drainage Kits Due to Sterility Concerns

    Aspen Surgical Products is recalling sterile wound drainage kits because the sterile barrier may be compromised, potentially exposing patients to infection.

    Product
    7mm Drain Kit Fluted 4 Channel with 100ml S-Vac Bulb, Sterile (10/case) Intended for closed wound suction drainage
    Category
    Medical Device
    Distribution
    35 states
  • HighNHTSA·14V177000·2014-04-11

    Mercedes-Benz Recalls C-Class Vehicles for Tail Light Electrical Defect

    Mercedes-Benz is recalling 2008-2011 C300, C350, and C63 AMG vehicles because a poor electrical ground may cause tail lights to dim or fail, increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, MERCEDES BENZ C350, C300, C63
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·14729·2014-04-10

    Whalen Recalls Stainless Steel Tool Chests Due to Laceration Hazard

    Whalen is recalling approximately 20,000 stainless steel tool chests sold at Costco due to a sharp metal edge on the right door that poses a laceration hazard.

    Product
    Stainless steel tool chests
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·14V190000·2014-04-10

    Forest River Recalls 2014 Vibe Travel Trailers for Incorrect Certification Labels

    Forest River is recalling 164 model year 2014 Vibe travel trailers because the Federal Certification Label lists incorrect tire and weight information, which could lead to overloading and tire failure.

    Product
    VIBE — VIBE VCT6504, VCT6501, VCT6502, VCT6503
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14E015000·2014-04-10

    Villa Recalls Defective Seat Belts in Jayco, Tiffin, and American Coach RVs

    Villa International is recalling specific driver and passenger seats used in 2014-2015 Jayco, Tiffin, and American Coach recreational vehicles because the seat belt attachment may be incorrect and the belt may fray, reducing its strength.

    Product
    JAYCO — JAYCO, TIFFIN, AMERICAN COACH ENTEGRA CORNERSTONE, ZEPHYR, ALLEGRO, AMERICAN TRADITION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·14146·2014-04-10

    BedHead Recalls Children's Pajamas for Flammability Standard Violations

    BedHead Pajamas Inc. is recalling about 800 children's two-piece pajama sets because they fail to meet federal flammability standards, posing a risk of burn injuries.

    Product
    Children's Two-Piece Pajama Sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1325-2014·2014-04-09

    Teleflex Recalls Weck Vista Optical Bladeless Laparoscopic Access Ports

    Teleflex Medical is recalling 55,521 Weck Vista Optical Bladeless Laparoscopic Access Ports due to complaints of insufflation gas leakage.

    Product
    5/10 mm Weck Vista Optical Bladeless Laparoscopic Access Port, Catalog No. 405910R; 5/10/12 mm Weck Vista Optical Bladeless Laparoscopic Access Port, Catalog No. 405912R. An endoscope and accessories is a device used to provide access, illumination, and allow observation or…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1324-2014·2014-04-09

    Teleflex Medical Recalls Weck Vista Cannulas Due to Gas Leakage

    Teleflex Medical is recalling 55,521 units of 10mm and 12mm Weck Vista Cannulas because they may leak insufflation gas.

    Product
    10mm Weck Vista Cannula-only, Catalog No. 405910C, 12mm Weck Vista Cannula-only, Catalog No. 405912C. An endoscope and accessories is a device used to provide access, illumination, and allow observation or manipulation of body cavities, hollow organs, and canals.
    Category
    Medical Device
    Distribution
    Distributed nationwide