The Recall Desk

Archive

September 2018 recalls

633 recalls were announced in September 2018.

What the numbers show

Critical
19
Severe
188
High
305
Moderate
102
Low
19

Of the 633 recalls this month scored against our rubric, 3% are Critical, 30% are Severe.

201–300 of 633

  • SevereFDA (Devices)·Z-3168-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Issue

    Zimmer Biomet is recalling Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Left 130¿ 13 mm x 360 mm, Item Number: 814613360
    Category
    Medical Device
    Distribution
    42 states
  • SevereFDA (Devices)·Z-3134-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Defect

    Zimmer Biomet is recalling 5,947 Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Right 130¿ 13 mm x 280 mm, Item Number: 814513280
    Category
    Medical Device
    Distribution
    42 states
  • SevereFDA (Devices)·Z-3136-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Set Screw Defect

    Zimmer Biomet is recalling 5,947 Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Right 130¿ 13 mm x 340 mm, Item Number: 814513340
    Category
    Medical Device
    Distribution
    42 states
  • SevereFDA (Devices)·Z-3095-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Defect

    Zimmer Biomet is recalling Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Left 125¿ 11 mm x 420 mm, Item Number: 814411420
    Category
    Medical Device
    Distribution
    42 states
  • SevereFDA (Devices)·Z-3053-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Defect

    Zimmer Biomet is recalling Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Right 125¿ 9 mm x 440 mm, Item Number: 814309440
    Category
    Medical Device
    Distribution
    42 states
  • SevereFDA (Devices)·Z-3086-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Set Screw Defect

    Zimmer Biomet is recalling 5,947 Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Left 125¿ 9 mm x 420 mm, Item Number: 814409420
    Category
    Medical Device
    Distribution
    42 states
  • SevereFDA (Devices)·Z-3166-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Defect

    Zimmer Biomet is recalling 5,947 Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Left 130¿ 13 mm x 320 mm, Item Number: 814613320
    Category
    Medical Device
    Distribution
    42 states
  • SevereFDA (Devices)·Z-3142-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Set Screw Defect

    Zimmer Biomet is recalling 5,947 Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Right 130¿ 15 mm x 320 mm, Item Number: 814515320
    Category
    Medical Device
    Distribution
    42 states
  • SevereFDA (Devices)·Z-3054-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Defect

    Zimmer Biomet is recalling 5,947 Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Right 125¿ 9 mm x 460 mm, Item Number: 814309460
    Category
    Medical Device
    Distribution
    42 states
  • SevereFDA (Devices)·Z-3099-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Set Screw Defect

    Zimmer Biomet is recalling 5,947 Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Left 125¿ 13 mm x 280 mm, Item Number: 814413280
    Category
    Medical Device
    Distribution
    42 states
  • SevereFDA (Devices)·Z-3065-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Defect

    Zimmer Biomet is recalling 5,947 Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Right 125¿ 11 mm x 460 mm, Item Number: 814311460
    Category
    Medical Device
    Distribution
    42 states
  • SevereFDA (Devices)·Z-3170-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Defect

    Zimmer Biomet is recalling Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Left 130¿ 13 mm x 400 mm, Item Number: 814613400
    Category
    Medical Device
    Distribution
    42 states
  • SevereFDA (Devices)·Z-3122-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Defect

    Zimmer Biomet is recalling Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Right 130¿ 11 mm x 280 mm, Item Number: 814511280
    Category
    Medical Device
    Distribution
    42 states
  • SevereFDA (Devices)·Z-3148-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Set Screw Issue

    Zimmer Biomet is recalling 5,947 Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Left 130¿ 9 mm x 320 mm, Item Number: 814609320
    Category
    Medical Device
    Distribution
    42 states
  • SevereFDA (Drugs)·D-1189-2018·2018-09-19

    SCA Pharmaceuticals Recalls Furosemide Injection Bags Due to Precipitate

    SCA Pharmaceuticals is recalling 1,384 bags of Furosemide injection due to visible precipitate. The product was distributed to three hospitals in DC, VA, and CT.

    Product
    Furosemide 100 mg added to 0.9% Sodium Chloride 100 mL Injection, 100 mL Single Dose Container bag, Rx Only, SCA Pharmaceuticals, 8821 Knoedl Ct., Little Rock, AR 72205, 877.550.5059, barcode 70004063032.
    Category
    Drug
    Distribution
    3 states
  • SevereNHTSA·18V643000·2018-09-19

    Livin' Lite CampLite Travel Trailers Recalled for Drawbar Crack Risk

    Livin' Lite is recalling 2017-2019 CampLite travel trailers because the drawbar may crack, causing the trailer to separate from the tow vehicle.

    Product
    LIVIN' LITE — LIVIN' LITE CAMPLITE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3058-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Defect

    Zimmer Biomet is recalling Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Right 125¿ 11 mm x 320 mm, Item Number: 814311320
    Category
    Medical Device
    Distribution
    42 states
  • SevereNHTSA·18V646000·2018-09-19

    Freightliner Recalls 2018-2019 Models Due to Steering Shaft Defect

    Daimler Trucks North America is recalling 2018-2019 Freightliner 108SD, 114SD, and Business Class M2 vehicles because an incorrectly installed steering shaft may disconnect the steering wheel from the front wheels.

    Product
    FREIGHTLINER — FREIGHTLINER 108SD, 114SD, BUSINESS CLASS M2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V641000·2018-09-19

    Daimler Trucks Recalls 2019 Freightliner and Western Star Trucks for Tire Defect

    Daimler Trucks is recalling 2019 Freightliner and Western Star trucks because exposed tire sidewall steel cords may cause rapid air loss, increasing crash risk.

    Product
    WESTERN STAR — WESTERN STAR, FREIGHTLINER 4900, 4700, BUSINESS CLASS M2, 108SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V647000·2018-09-19

    Spartan Metrostar Emergency Vehicles Recalled for Wheel Stud Defect

    Spartan Motors is recalling 2018-2019 Metrostar emergency vehicles because improperly heat-treated wheel studs may fail, potentially causing the wheel to detach.

    Product
    SPARTAN — SPARTAN METROSTAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3128-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Defect

    Zimmer Biomet is recalling 5,947 Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Right 130¿ 11 mm x 400 mm, Item Number: 814511400
    Category
    Medical Device
    Distribution
    42 states
  • SevereFDA (Devices)·Z-3090-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Defect

    Zimmer Biomet is recalling Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Left 125¿ 11 mm x 320 mm, Item Number: 814411320
    Category
    Medical Device
    Distribution
    42 states
  • SevereFDA (Devices)·Z-3167-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Defect

    Zimmer Biomet is recalling Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Left 130¿ 13 mm x 340 mm, Item Number: 814613340
    Category
    Medical Device
    Distribution
    42 states
  • SevereFDA (Devices)·Z-3151-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Set Screw Defect

    Zimmer Biomet is recalling 5,947 Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Left 130¿ 9 mm x 420 mm, Item Number: 814609420
    Category
    Medical Device
    Distribution
    42 states
  • SevereFDA (Devices)·Z-3087-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Defect

    Zimmer Biomet is recalling 5,947 Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Left 125¿ 9 mm x 440 mm, Item Number: 814409440
    Category
    Medical Device
    Distribution
    42 states
  • SevereFDA (Devices)·Z-3049-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Set Screw Defect

    Zimmer Biomet is recalling 5,947 Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Right 125¿ 9 mm x 320 mm, Item Number: 814309320
    Category
    Medical Device
    Distribution
    42 states
  • SevereFDA (Devices)·Z-3060-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Defect

    Zimmer Biomet is recalling 5,947 Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Right 125¿ 11 mm x 360 mm, Item Number: 814311360
    Category
    Medical Device
    Distribution
    42 states
  • SevereFDA (Devices)·Z-3048-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Issue

    Zimmer Biomet is recalling Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Right 125¿ 9 mm x 300 mm, Item Number 814309300
    Category
    Medical Device
    Distribution
    42 states
  • SevereFDA (Devices)·Z-3074-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Defect

    Zimmer Biomet is recalling Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Right 125¿ 13 mm x 400 mm, Item Number: 814313400
    Category
    Medical Device
    Distribution
    42 states
  • SevereFDA (Devices)·Z-3129-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Defect

    Zimmer Biomet is recalling 5,947 Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Right 130¿ 11 mm x 420 mm, Item Number: 814511420
    Category
    Medical Device
    Distribution
    42 states
  • SevereFDA (Devices)·Z-3097-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Defect

    Zimmer Biomet is recalling Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Left 125¿ 11 mm x 460 mm, Item Number: 814411460
    Category
    Medical Device
    Distribution
    42 states
  • SevereFDA (Devices)·Z-3132-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Defect

    Zimmer Biomet is recalling 5,947 Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail 130¿ 13 mm x 180 mm, Item Number: 814513180
    Category
    Medical Device
    Distribution
    42 states
  • SevereFDA (Devices)·Z-3172-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Defect

    Zimmer Biomet is recalling 5,947 Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Left 130¿ 13 mm x 440 mm, Item Number: 814613440
    Category
    Medical Device
    Distribution
    42 states
  • SevereFDA (Devices)·Z-3107-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Defect

    Zimmer Biomet is recalling Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Left 125¿ 13 mm x 460 mm, Item Number: 814413460
    Category
    Medical Device
    Distribution
    42 states
  • SevereFDA (Devices)·Z-3104-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Issue

    Zimmer Biomet is recalling Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Left 125¿ 13 mm x 380 mm, Item Number: 814413380
    Category
    Medical Device
    Distribution
    42 states
  • SevereFDA (Devices)·Z-3146-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Set Screw Defect

    Zimmer Biomet is recalling 5,947 Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Left 130¿ 9 mm x 260 mm, Item Number: 814609260
    Category
    Medical Device
    Distribution
    42 states
  • SevereFDA (Devices)·Z-3153-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Defect

    Zimmer Biomet is recalling 5,947 Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Left 130¿ 11 mm x 260 mm, Item Number: 814611260
    Category
    Medical Device
    Distribution
    42 states
  • SevereFDA (Devices)·Z-3154-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Set Screw Defect

    Zimmer Biomet is recalling 5,947 Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Left 130¿ 11 mm x 280 mm, Item Number: 814611280
    Category
    Medical Device
    Distribution
    42 states
  • SevereFDA (Devices)·Z-3137-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Defect

    Zimmer Biomet is recalling Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Right 130¿ 13 mm x 380 mm, Item Number: 814513380
    Category
    Medical Device
    Distribution
    42 states
  • SevereFDA (Devices)·Z-3057-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Defect

    Zimmer Biomet is recalling 5,947 Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Right 125¿ 11 mm x 300 mm, Item Number: 814311300
    Category
    Medical Device
    Distribution
    42 states
  • SevereFDA (Devices)·Z-3140-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Set Screw Defect

    Zimmer Biomet is recalling 5,947 Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Right 130¿ 13 mm x 440 mm, Item Number: 814513440
    Category
    Medical Device
    Distribution
    42 states
  • SevereFDA (Devices)·Z-3155-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Defect

    Zimmer Biomet is recalling Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Left 130¿ 11 mm x 320 mm, Item Number: 814611320
    Category
    Medical Device
    Distribution
    42 states
  • SevereFDA (Devices)·Z-3174-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Set Screw Defect

    Zimmer Biomet is recalling Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Left 130¿ 15 mm x 360 mm, Item Number: 814615360
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-3047-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Defect

    Zimmer Biomet is recalling 5,947 Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail 125¿ 9 mm x 180 mm, Item Number: 814309180
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-3066-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Defect

    Zimmer Biomet is recalling 5,947 Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Right 125¿ 13 mm x 180 mm, Item Number: 814313180
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-3079-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Set Screw Defect

    Zimmer Biomet is recalling 5,947 Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Left 125¿ 9 mm x 280 mm, Item Number: 814409280
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-3085-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Defect

    Zimmer Biomet is recalling 5,947 Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Left 125¿ 9 mm x 400 mm, Item Number: 814409400
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-3116-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Defect

    Zimmer Biomet is recalling Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Right 130¿ 9 mm x 400 mm, Item Number: 814509400
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-3115-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Issue

    Zimmer Biomet is recalling Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Right 130¿ 9 mm x 380 mm, Item Number: 814509380
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-3145-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Issue

    Zimmer Biomet is recalling Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Right 130¿ 15 mm x 440 mm, Item Number: 814515440
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-3149-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Defect

    Zimmer Biomet is recalling Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Left 130¿ 9 mm x 360 mm, Item Number: 814609360
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-2995-2018·2018-09-19

    Ohio Medical Care-E-Vac 3 Portable Suction Pump Recall

    Ohio Medical is recalling 1,443 Care-E-Vac 3 portable suction pumps because a battery terminal may contact the pump, causing an electric short and loss of function.

    Product
    Portable Suction Pump, (a) Style 758010, Model CARE-E-VAC 3, Ohio Medical LLC; (b) Style 758000, Model CARE-E-VAC 3, Ohio Medical LLC The care-e-(R)3 is a portable medical aspirator used to suction fluids or foreign bodies from a patient. The primary intended use is to aspira
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3118-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Defect

    Zimmer Biomet is recalling Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Right 130¿ 9 mm x 440 mm, Item Number: 814509440
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-3173-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Defect

    Zimmer Biomet is recalling Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Left 130¿ 13 mm x 460 mm, Item Number: 814613460
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-3112-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Set Screw Defect

    Zimmer Biomet is recalling 5,947 Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Right 130¿ 9 mm x 320 mm, Item Number: 814509320
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-3164-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Defect

    Zimmer Biomet is recalling Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Left 130¿ 13 mm x 280 mm, Item Number: 814613280
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-3150-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Issue

    Zimmer Biomet is recalling 5,947 Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Left 130¿ 9 mm x 400 mm, Item Number: 814609400
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-3143-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Set Screw Defect

    Zimmer Biomet is recalling Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Right 130¿ 15 mm x 360 mm, Item Number: 814515360
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-3160-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Set Screw Defect

    Zimmer Biomet is recalling 5,947 Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Left 130¿ 11 mm x 420 mm, Item Number: 814611420
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-3088-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Defect

    Zimmer Biomet is recalling Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Left 125¿ 9 mm x 460 mm, Item Number: 814409460
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-3055-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Defect

    Zimmer Biomet is recalling 5,947 Affixus Hip Fracture Nail 125 units because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail 125¿ 11 mm x 180 mm, Item Number: 814311180
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-3125-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Set Screw Defect

    Zimmer Biomet is recalling 5,947 Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Right 130¿ 11 mm x 340 mm, Item Number: 814511340
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-3071-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Defect

    Zimmer Biomet is recalling Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Right 125¿ 13 mm x 340 mm, Item Number: 814313340
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-3080-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Defect

    Zimmer Biomet is recalling Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Left 125¿ 9 mm x 300 mm, Item Number: 814409300
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-3159-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Set Screw Defect

    Zimmer Biomet is recalling 5,947 Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Left 130¿ 11 mm x 400 mm, Item Number: 814611400
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-3171-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Defect

    Zimmer Biomet is recalling Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Left 130¿ 13 mm x 420 mm, Item Number: 814613420
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-3092-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Defect

    Zimmer Biomet is recalling Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Left 125¿ 11 mm x 360 mm, Item Number: 814411360
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-3067-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Defect

    Zimmer Biomet is recalling Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Right 125¿ 13 mm x 260 mm, Item Number: 814313260
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-3158-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Defect

    Zimmer Biomet is recalling Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Left 130¿ 11 mm x 380 mm, Item Number: 814611380
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-3131-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Defect

    Zimmer Biomet is recalling Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Right 130¿ 11 mm x 460 mm, Item Number: 814511460
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-3117-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Issue

    Zimmer Biomet is recalling Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Right 130¿ 9 mm x 420 mm, Item Number: 814509420
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-3157-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Defect

    Zimmer Biomet is recalling Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Left 130¿ 11 mm x 360 mm, Item Number: 814611360
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-3023-2018·2018-09-19

    NordicNeuroLab Recalls fMRI LCD Monitor Power Supplies Due to Magnet Bore Risk

    NordicNeuroLab AS is recalling 163 LCD monitor power supplies for fMRI systems because they were reported to be dragged into the magnet bore.

    Product
    fMRI Hardware System VisualSystem allows video signals from the stimulus presentation PC to enter the shielded scanner room and presented by a set of coil-mounted displays or by an in-room LCD monitor. - LCD Monitor Power supply (LPS) for LCD Monitor, Versions 1.0 and 1.1
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-3119-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Defect

    Zimmer Biomet is recalling Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Right 130¿ 9 mm x 460 mm, Item Number: 814509460
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-3103-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Issue

    Zimmer Biomet is recalling Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Left 125¿ 13 mm x 360 mm, Item Number: 814413360
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-3169-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Defect

    Zimmer Biomet is recalling 5,947 Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Left 130¿ 13 mm x 380 mm, Item Number: 814613380
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-3076-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Defect

    Zimmer Biomet is recalling Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Right 125¿ 13 mm x 440 mm, Item Number: 814313440
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-3152-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Defect

    Zimmer Biomet is recalling 5,947 Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Left 130¿ 9 mm x 460 mm, Item Number: 814609460
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-3138-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Defect

    Zimmer Biomet is recalling Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Right 130¿ 13 mm x 400 mm, Item Number: 814513400
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-3163-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Defect

    Zimmer Biomet is recalling Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Left 130¿ 13 mm x 260 mm, Item Number: 814613260
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Food)·F-1977-2018·2018-09-19

    Air Stream Corp. Recalls Brussel Sprouts Due to Listeria Risk

    Air Stream Corp. is recalling Brussel Sprouts because they may be contaminated with Listeria monocytogenes. The product was distributed in several Northeastern and Mid-Atlantic states.

    Product
    Brussel Sprouts
    Category
    Food
    Distribution
    7 states
  • HighFDA (Devices)·Z-3078-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Defect

    Zimmer Biomet is recalling Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Left 125¿ 9 mm x 260 mm, Item Number: 814409260
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-3096-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Defect

    Zimmer Biomet is recalling Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Left 125¿ 11 mm x 440 mm, Item Number: 814411440
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-3081-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Set Screw Defect

    Zimmer Biomet is recalling 5,947 Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Left 125¿ 9 mm x 320 mm, Item Number: 814409320
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-3063-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Set Screw Defect

    Zimmer Biomet is recalling 5,947 Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Right 125¿ 11 mm x 420 mm, Item Number: 814311420
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Food)·F-1979-2018·2018-09-19

    Air Stream Corp. Recalls Shredded Green Cabbage Due to Listeria Risk

    Air Stream Corp. is recalling shredded green cabbage potentially contaminated with Listeria monocytogenes. The product was distributed across several Northeastern and Mid-Atlantic states.

    Product
    Shredded green cabbage
    Category
    Food
    Distribution
    7 states
  • HighFDA (Devices)·Z-3156-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Set Screw Defect

    Zimmer Biomet is recalling 5,947 Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Left 130¿ 11 mm x 340 mm, Item Number: 814611340
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Food)·F-1981-2018·2018-09-19

    Aztlan Mole Oaxaqueno Negro Recalled for Undeclared Milk, Wheat, and Soy Allergens

    Hidroponicos Brownia is recalling Aztlan Mole Oaxaqueno Negro because milk, wheat, and soy were not declared on the label.

    Product
    Aztlan Mole Oaxaqueno Negro; 10 kg plastic buckets (22 lbs); Ingredients: sugar, Ancho pepper, peanut, soybean oil, pasilla pepper, guajillo pepper, sesame seed, cookie, cocoa, corn flour, idozided salt, condiments and spices. Sodium benzoate as a preservative. Distribute
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-3162-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Set Screw Defect

    Zimmer Biomet is recalling Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Left 130¿ 11 mm x 460 mm, Item Number: 814611460
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Food)·F-1978-2018·2018-09-19

    Air Stream Corp. Recalls Radicchio Due to Listeria Contamination Risk

    Air Stream Corp. is recalling 10 lb bags of Radicchio because the product may be contaminated with Listeria monocytogenes. The recall covers distribution in seven Northeastern and Mid-Atlantic states.

    Product
    Radicchio, 10 lbs
    Category
    Food
    Distribution
    7 states
  • HighFDA (Devices)·Z-3045-2018·2018-09-19

    Beaver Accu-Temp High Temperature Cautery Recalled for Sterility Risk

    Beaver Visitec is recalling 800 units of Accu-Temp High Temperature Cautery devices due to a potential loss of sterility caused by packaging defects.

    Product
    Beaver Accu-Temp High Temperature Cautery, 2 inch Shaft with Fine Tip, Model Number 8445000 Product Usage: The indications and intended use of the High Temp cautery are for coagulating tissue or arresting bleeding from small vessels by heat conducted through the wire tip. Indi
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3114-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Set Screw Issue

    Zimmer Biomet is recalling 5,947 Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Right 130¿ 9 mm x 360 mm, Item Number: 814509360
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-3056-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Defect

    Zimmer Biomet is recalling Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Right 125¿ 11 mm x 280 mm, Item Number: 814311280
    Category
    Medical Device
    Distribution
    42 states

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