The Recall Desk

Archive

March 2017 recalls

854 recalls were announced in March 2017.

What the numbers show

Critical
90
Severe
243
High
356
Moderate
134
Low
31

Of the 854 recalls this month scored against our rubric, 11% are Critical, 28% are Severe.

601–700 of 854

  • HighFDA (Devices)·Z-1392-2017·2017-03-08

    Cook Inc. Recalls Check-Flo Introducer Devices Due to Blood Loss Reports

    Cook Inc. is recalling 29 Check-Flo Introducer Hausdorf-Lock Atrial devices worldwide due to increased reports of blood loss associated with the hemostatic valve design.

    Product
    Check-Flo Introducer Hausdorf-Lock Atrial, Individual product is packaged in a Tyvek-film sterilizable outer pouch. Introducers are intended for introduction of balloons, closed and non-tapered end catheters or other diagnostic and interventional devices
    Category
    Medical Device
    Distribution
    46 states
  • HighFDA (Devices)·Z-1276-2017·2017-03-08

    Windstone Medical Packaging Recalls Breast Augmentation Kits Due to Sterility Concerns

    Windstone Medical Packaging is recalling 1,436 breast augmentation kits because the disposable gloves included may contain splits or holes that compromise sterility.

    Product
    Breast Augmentation Pack, part number AMS1786(A Breast Augmentation Pack, part number AMS2790(A Breast Augmentation Pack, part number AMS3324(B Breast Augmentation Pack, part number AMS4382 Breast Augmentation Pack, part number AMS4382(A Breast Augmentation Pack, part…
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1291-2017·2017-03-08

    Medtronic Disposable Gloves Recalled for Potential Sterility Compromise

    Windstone Medical Packaging is recalling Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES in custom kits because splits or holes may compromise sterility.

    Product
    Dr. Casey Pack, part number AMS4313(A
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1389-2017·2017-03-08

    Cook Inc. Recalls Check-Flo Hemostasis Assemblies Due to Blood Loss Reports

    Cook Inc. is recalling 1,589 Check-Flo Hemostasis Assemblies because reports indicate increased blood loss associated with the device's valve design.

    Product
    Check-Flo Hemostasis Assembly, Individual product is packaged in a Tyvek-film sterilizable outer pouch.
    Category
    Medical Device
    Distribution
    46 states
  • HighFDA (Devices)·Z-1264-2017·2017-03-08

    Medtronic Disposable Gloves Recalled for Potential Sterility Compromise

    Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES in Aligned Medical Solutions kits are recalled because splits or holes may compromise sterility.

    Product
    Basic Extended Pack, part number AMS4421(A Basic Extended Pack, part number AMS4421(B
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1311-2017·2017-03-08

    Medtronic Disposable Gloves Recalled for Sterility Compromise

    Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES in Aligned Medical Solutions kits are recalled because splits or holes may compromise sterility.

    Product
    Hand Pack, part number AMS3640 Hand Pack, part number AMS4213(A Hand Pack, part number AMS4311(A Hand Pack, part number AMS5343 Hand Pack., part number PSS1843(A
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1259-2017·2017-03-08

    Medtronic Gloves in AMS Kits Recalled for Sterility Compromise

    Windstone Medical Packaging is recalling 174 Angio Pack kits because the Medtronic gloves inside may have splits or holes that compromise sterility.

    Product
    Angio Pack, part number AMS6711
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1266-2017·2017-03-08

    Windstone Medical Packaging Recalls Basic Kits with Defective Gloves

    Windstone Medical Packaging is recalling 216 Basic Kits because the included Medtronic gloves may contain splits or holes that compromise sterility.

    Product
    Basic Kit, part number CMP1109(A
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1356-2017·2017-03-08

    Windstone Medical Recalls Pacemaker Kits Due to Sterility Compromise

    Windstone Medical Packaging is recalling 561 pacemaker kits because the disposable gloves included may contain splits or holes that compromise sterility.

    Product
    Pacemaker Kit, part number AMS4281 Pacemaker Kit, part number AMS4281(A Pacemaker Kit, part number AMS4281(C Pacemaker Kit, part number AMS4281(D
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Food)·F-1544-2017·2017-03-08

    World Organic Recalls Vitamins Due to Allergen Labeling Errors

    World Organic Corp. is recalling Theravits 100 and The Supreme One vitamins because the labels incorrectly state they contain no common allergens while containing fish liver oil.

    Product
    Theravits 100, container sizes: 30, 60, 90, 180, Product Code: 0783-30, 0786-60, 0789-90, 0788-180; The Supreme One, Container sizes: 30,60,90,180, Product Code: 680-030, 680-060, 680-090, 680-180. The Supreme One and Theravits 100 product is sold under the brand names of…
    Category
    Food
    Distribution
    10 states
  • HighFDA (Devices)·Z-1387-2017·2017-03-08

    Cook Inc. Recalls Check-Flo Performer Introducers Due to Blood Loss Reports

    Cook Inc. is recalling 884 Check-Flo Performer Introducers because a specific valve design is associated with increased reports of blood loss.

    Product
    Check-Flo Performer Introducer, Individual product is packaged in a Tyvek-film sterilizable outer pouch. Introducers are intended for introduction of balloons, closed and non-tapered end catheters or other diagnostic and interventional devices.
    Category
    Medical Device
    Distribution
    46 states
  • HighFDA (Devices)·Z-1315-2017·2017-03-08

    Windstone Medical Recalls Hernia Packs with Defective Gloves

    Windstone Medical Packaging is recalling 228 Hernia Packs because the included Medtronic gloves may have splits or holes that compromise sterility.

    Product
    Hernia Pack, part number AMS3859
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1292-2017·2017-03-08

    Windstone Medical Recalls Dr. Landi EVLT Packs Due to Sterility Concerns

    Windstone Medical Packaging is recalling 944 Dr. Landi EVLT Packs because the included Medtronic gloves may have splits or holes that compromise sterility.

    Product
    Dr. Landi EVLT Pack, part number AMS1483(E Dr. Landi EVLT Pack, part number AMS1483(E
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1284-2017·2017-03-08

    Medtronic Disposable Gloves Recalled for Potential Sterility Compromise

    Windstone Medical Packaging is recalling Medtronic disposable gloves in custom kits because splits or holes may compromise sterility.

    Product
    Custom Pack, part number AMS4776 Custom Pack, part number AMS4776(A Custom Pack, part number AMS5643 Custom Pack, part number AMS5643(A Custom Pack, part number AMS6012 Custom Pack, part number AMS6383 Custom Pack, part number PSS2135(B Custom Pack, part number PSS2798(B…
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1319-2017·2017-03-08

    Medtronic Disposable Gloves Recalled for Potential Sterility Compromise

    Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES in custom AMS kits are being recalled because splits or holes may compromise sterility.

    Product
    Hysteroscopy Pack, part number AMS4797 Hysteroscopy Pack, part number AMS4797(A Hysteroscopy Pack, part number AMS4797(B
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1364-2017·2017-03-08

    Windstone Medical Packaging Recalls Reduction Mammoplasty Packs Due to Sterility Concerns

    Windstone Medical Packaging is recalling 35 Reduction Mammoplasty Packs because the included Medtronic gloves may contain splits or holes that compromise sterility.

    Product
    Reduction Mammoplasty Pack, part number AMS4380 Reduction Mammoplasty Pack, part number AMS4380(B
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1324-2017·2017-03-08

    Medtronic Gloves in AMS Lap Band Kits Recalled for Sterility Risk

    Windstone Medical Packaging is recalling 252 Lap Band kits because the included Medtronic gloves may have splits or holes that compromise sterility.

    Product
    Lap Band Pack, part number AMS1785(A
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1336-2017·2017-03-08

    Windstone Medical Recalls Lumbar Laminectomy Packs Due to Sterility Concerns

    Windstone Medical Packaging is recalling 123 Lumbar Laminectomy Packs because the included gloves may have splits or holes that compromise sterility.

    Product
    Lumbar Laminectomy Pack, part number AMS2501 Lumbar Laminectomy Pack, part number AMS2501(A Lumbar Laminectomy Pack, part number AMS2501(B
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1345-2017·2017-03-08

    Medtronic Disposable Gloves Recalled for Potential Sterility Compromise

    Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES in custom Aligned Medical Solutions kits are recalled because splits or holes may compromise sterility.

    Product
    Morris Hysto Pack, part number PSS3198(A
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1393-2017·2017-03-08

    Cook Inc. Recalls TriForce Peripheral Crossing Sets Due to Blood Loss Reports

    Cook Inc. is recalling 1,875 TriForce Peripheral Crossing Sets because a specific valve design is associated with increased reports of blood loss.

    Product
    TriForce Peripheral Crossing Set, Individual product is packaged in a Tyvek-film sterilizable outer pouch. The TriForce Peripheral Crossing Set is intended to be percutaneously introduced into blood vessels and support a wire guide while performing percutaneous peripheral…
    Category
    Medical Device
    Distribution
    46 states
  • HighNHTSA·17V150000·2017-03-08

    Audi Recalls 2017 A5 and S5 Cabriolets for Seat Belt Pretensioner Defect

    Volkswagen Group of America is recalling 2017 Audi A5 and S5 Cabriolets because a seat belt pretensioner component may detach during a crash, creating a projectile hazard.

    Product
    AUDI — AUDI S5 CABRIOLET, A5 CABRIOLET
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1330-2017·2017-03-08

    Windstone Medical Recalls Laparoscopic Packs Due to Sterility Concerns

    Windstone Medical Packaging is recalling 1,056 Laparoscopic Packs because the included Medtronic gloves may contain splits or holes that compromise sterility.

    Product
    Laparoscopic Pack, part number AMS2499 Laparoscopic Pack, part number AMS2499(A Laparoscopic Pack, part number AMS2499(B
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1344-2017·2017-03-08

    Medtronic Disposable Gloves Recalled for Potential Sterility Compromise

    Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES in Aligned Medical Solutions kits are recalled because splits or holes may compromise sterility.

    Product
    Minor/General/Ortho Pack, part number PSS3258(B
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1391-2017·2017-03-08

    Cook Inc. Recalls Micropuncture Check-Flo Performer Introducer Sets Due to Blood Loss

    Cook Inc. is recalling 778 Micropuncture Check-Flo Performer Introducer Sets because a specific valve design is associated with increased reports of blood loss.

    Product
    Micropuncture Check-Flo Performer Introducer Set, Individual product is packaged in a Tyvek-film sterilizable outer pouch. Introducers are intended for introduction of balloons, closed and non-tapered end catheters or other diagnostic and interventional devices
    Category
    Medical Device
    Distribution
    46 states
  • HighFDA (Devices)·Z-1357-2017·2017-03-08

    Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES Recalled for Sterility Compromise

    Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES in custom Aligned Medical Solutions kits are recalled because splits or holes may compromise sterility.

    Product
    Percutaneous Entry Kit, part number TVS4022(D Percutaneous Entry Kit , part number TVS4022(E Percutaneous Entry Kit, part number TVS4022(F
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1340-2017·2017-03-08

    Medtronic Gloves in AMS Kits Recalled for Sterility Compromise

    Windstone Medical Packaging is recalling 39 Major Pack kits containing Medtronic gloves that may have splits or holes compromising sterility.

    Product
    Major Pack (1345), part number AMS6565
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1354-2017·2017-03-08

    Windstone Medical Recalls Ortho Minor Packs Due to Sterility Compromise

    Windstone Medical Packaging is recalling 664 Ortho Minor Packs because the included disposable gloves may contain splits or holes that compromise sterility.

    Product
    Ortho Minor Pack, part number AMS3710(A
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1342-2017·2017-03-08

    Windstone Medical Minor Procedure Packs Recalled for Sterility Compromise

    Windstone Medical Packaging is recalling 365 Minor Procedure Packs because the included Medtronic gloves may contain splits or holes that compromise sterility.

    Product
    Minor Procedure Pack, part number AMS4799
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1261-2017·2017-03-08

    Windstone Medical Arthroscopy Packs Recalled for Sterility Compromise

    Windstone Medical Packaging is recalling 1,081 arthroscopy kits because the disposable gloves inside may have splits or holes that compromise sterility.

    Product
    Arthroscopy Pack, part number AMS2938 Arthroscopy Pack, part number AMS3639 Arthroscopy Pack, part number AMS4765 Arthroscopy Pack, part number PSS1799 Arthroscopy Pack, part number PSS1845(A
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1305-2017·2017-03-08

    Windstone Medical Packaging Recalls General Packs with Defective Gloves

    Windstone Medical Packaging is recalling 1,501 General Packs because the included Medtronic gloves may contain splits or holes that compromise sterility.

    Product
    General Pack, part number AMS2967(A General Pack, part number AMS3239(A General Pack, part number AMS3709(B General Pack, part number AMS5341 General Pack, part number AMS5694
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1390-2017·2017-03-08

    Cook Inc. Recalls Flexor Radial Access Sets Due to Blood Loss Reports

    Cook Inc. is recalling 41,975 Flexor Radial Access Sets because a specific hemostatic valve design is associated with increased reports of blood loss.

    Product
    Flexor Radial Access Set, Individual product is packaged in a Tyvek-film sterilizable outer pouch. The Flexor¿ Radial Hydrophilic Introducer Access Set is intended to introduce diagnostic and interventional devices In radial artery access procedures
    Category
    Medical Device
    Distribution
    46 states
  • HighFDA (Devices)·Z-1298-2017·2017-03-08

    Medtronic Disposable Gloves Recalled for Potential Sterility Compromise

    Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES in custom Aligned Medical Solutions kits are recalled because splits or holes may compromise sterility.

    Product
    Eye Plastic Tray, part number PSS1931(A
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Food)·F-1546-2017·2017-03-08

    Bell Stone Toffee Recalls Chocolate Products Due to Undeclared Milk Allergen

    Bell Stone Toffee is voluntarily recalling specific lots of toffee products because the labels failed to identify milk as an ingredient, despite declaring butter.

    Product
    Dark Chocolate Toffee, 2.2oz pouches, 6oz pouches, 7oz boxes, one pound boxes
    Category
    Food
    Distribution
    7 states
  • HighFDA (Devices)·Z-1339-2017·2017-03-08

    Windstone Medical Recalls Major Laparotomy Packs Due to Sterility Concerns

    Windstone Medical Packaging is recalling 32 Major Laparotomy Packs because the disposable gloves included may have splits or holes that compromise sterility.

    Product
    Major Laparotomy Pack - NS, part number AMS4347
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1278-2017·2017-03-08

    Medtronic Disposable Gloves Recalled for Potential Sterility Compromise

    Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES in Aligned Medical Solutions kits are recalled because splits or holes may compromise sterility.

    Product
    Breast Recon Pack, part number AMS5698 Breast Recon Pack, part number AMS5698(A
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1361-2017·2017-03-08

    Medtronic Disposable Gloves Recalled for Potential Sterility Compromise

    Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES in custom Aligned Medical Solutions kits are recalled because splits or holes may compromise sterility.

    Product
    Plastic Pack, part number PSS2462 Plastic Pack, part number PSS3319 Plastic Pack, part number PSS3319(A
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1385-2017·2017-03-08

    Merge Healthcare Recalls Unity PACS Software Due to Image Error

    Merge Healthcare is recalling Unity PACS software versions 11.0 and 11.0.1 because the software fails to add the correct tomo image.

    Product
    DR Systems Unity PACS software, now known as Merge Unity PACS. Product Usage: Merge Unity PACS is a medical image and information management system that allows viewing, selection, processing, printing, telecommunications, and media interchange of medical images from a…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1386-2017·2017-03-08

    Maquet CARDIOSAVE IABP Li-Ion Battery Recall Due to Venting Risk

    Maquet is recalling Li-Ion batteries for CARDIOSAVE IABP devices after reports of venting when dropped.

    Product
    CARDIOSAVE Hybrid IABP and CARDIOSAVE Rescue IABP affected part number is 0998-:XX-0800-XX Li-Ion Battery affected part number is 0146-00-0097 Product Usage: The CARDIOSAVE Hybrid Intra-Aortic Balloon Pump (IABP) is an electromechanical system used to inflate and deflate…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1283-2017·2017-03-08

    FDA Recalls Custom Breast Augmentation Packs Due to Sterility Concerns

    Windstone Medical Packaging is recalling 229 Custom Breast Augmentation Packs because the included gloves may have splits or holes that compromise sterility.

    Product
    Custom Breast Augmentation Pack, part number PSS2455(D
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1253-2017·2017-03-08

    Phadia Recalls EliA Sample Diluent Due to Liquid Level Detection Issues

    Phadia US Inc is recalling EliA Sample Diluent because liquid level detection problems in Phadia 250 instruments caused erroneous test results.

    Product
    EliA Sample Diluent, Article number, 83-1023-01
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1383-2017·2017-03-08

    Synthes Recalls Mislabelled PRODISC Orthopedic Spinal Surgery Struts

    Synthes (USA) Products LLC is recalling two PRODISC Orthopedic Manual Surgical Instrument struts used in spinal surgery because they are incorrectly etched and labeled with the wrong size.

    Product
    PRODISC Orthopedic Manual Surgical Instrument, strut used in spinal surgery. Part numbers 03.820.350 and 03.820.352. Used to hold the disc segment open and facilitate discectomy
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Devices)·Z-1381-2017·2017-03-08

    Medtronic Gloves in Custom Kits Recalled for Sterility Compromise

    Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES in custom Aligned Medical Solutions kits are being recalled because splits or holes may compromise sterility.

    Product
    Vein Tray, part number AMS6312
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1258-2017·2017-03-08

    Windstone Medical Abdominoplasty Kits Recalled for Sterility Compromise

    Windstone Medical Packaging is recalling 45 Abdominoplasty Kits because the included Medtronic gloves may contain splits or holes that compromise sterility.

    Product
    Abdominoplasty Pack, Part numbers AMS3326(B, AMS4381, and AMS4381(B.
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1370-2017·2017-03-08

    Windstone Medical Spine Pack Gloves Recalled for Sterility Compromise

    Windstone Medical Packaging recalled 286 Spine Pack kits because the disposable gloves may contain splits or holes that compromise sterility.

    Product
    Spine Pack , part number AMS3753(A Spine Pack, part number AMS3783(A Spine Pack, part number AMS3783(B Spine Pack, part number AMS6472
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1341-2017·2017-03-08

    Windstone Medical Minor Packs Recalled for Potential Sterility Compromise

    Windstone Medical Packaging is recalling 665 Minor Packs because the included Medtronic gloves may have splits or holes that compromise sterility.

    Product
    Minor Pack, part number AMS3782(B Minor Pack, part number AMS3782(C Minor Pack, part number CMP1560 Minor Pack, part number PSS3518(B Minor Pack, part number PSS3541(A
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1360-2017·2017-03-08

    Medtronic Disposable Gloves Recalled for Sterility Compromise

    Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES in custom Aligned Medical Solutions kits are recalled because splits or holes may compromise sterility.

    Product
    Plastic Kit, part number CMP1084(C
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1326-2017·2017-03-08

    Windstone Medical Recalls Lap Gallbladder Packs Due to Sterility Concerns

    Windstone Medical Packaging is recalling 225 Lap Gallbladder Packs because the included Medtronic gloves may have splits or holes that compromise sterility.

    Product
    Lap Gallbladder Pack, part number AMS3707
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1378-2017·2017-03-08

    Medtronic Gloves in AMS Kits Recalled for Sterility Compromise

    Windstone Medical Packaging is recalling 1,787 Upper Extremity Packs because the Medtronic gloves inside may have splits or holes that compromise sterility.

    Product
    Upper Extremity Pack, part number AMS4670 Upper Extremity Pack, part number AMS4670(A
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1290-2017·2017-03-08

    Medtronic Disposable Gloves Recalled for Potential Sterility Compromise

    Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES in Aligned Medical Solutions kits are being recalled because splits or holes may compromise sterility.

    Product
    Dr Bragg Vein Tray - RX, part number 007912-8
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1285-2017·2017-03-08

    Windstone Medical Packaging Recalls Custom Kits with Defective Gloves

    Windstone Medical Packaging is recalling 840 custom kits because the included Medtronic gloves may contain splits or holes that compromise sterility.

    Product
    Custom Pack - with Introducer Kit, part number TVS4011NI(L
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1346-2017·2017-03-08

    Windstone Medical Recalls Morris Lap Packs Due to Sterility Compromise

    Windstone Medical Packaging is recalling Morris Lap Packs because the disposable gloves included in the kits may contain splits or holes that compromise sterility.

    Product
    Morris Lap Pack, part number PSS3199(A
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1320-2017·2017-03-08

    Windstone Medical Recalls Knee Arthroscopy Packs Due to Sterility Concerns

    Windstone Medical Packaging is recalling 700 knee arthroscopy packs because the disposable gloves included may have splits or holes that compromise sterility.

    Product
    Knee Arthroscopy Pack , part number AMS2610(A Knee Arthroscopy Pack, part number AMS3236(A Knee Arthroscopy Pack, part numbre AMS3860
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1297-2017·2017-03-08

    Medtronic Disposable Gloves Recalled for Potential Sterility Compromise

    Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES in custom Aligned Medical Solutions kits are being recalled because they may contain splits or holes that compromise sterility.

    Product
    Extremity Pack-N Brunswick, part number PSS1866(A
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1277-2017·2017-03-08

    Medtronic Disposable Gloves Recalled for Potential Sterility Compromise

    Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES in custom Aligned Medical Solutions kits are recalled because splits or holes may compromise sterility.

    Product
    Breast Pack, part number AMS3238(A Breast Pack, part number AMS4419(A Breast Pack, part number AMS4419(B Breast Pack, part number AMS5750 Breast Pack, part number AMS5750(A Breast Pack, part number AMS6120 Breast Pack, part number PSS1784(B Breast Pack, part number…
    Category
    Medical Device
    Distribution
    26 states

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