The Recall Desk

Archive

July 2018 recalls

502 recalls were announced in July 2018.

What the numbers show

Critical
34
Severe
167
High
225
Moderate
62
Low
14

Of the 502 recalls this month scored against our rubric, 7% are Critical, 33% are Severe.

Which agencies issued them

101–200 of 502

  • HighFDA (Drugs)·D-0948-2018·2018-07-25

    Avella Recalls Heparin Bags Due to Potential Leakage and Sterility Concerns

    Avella of Deer Valley, Inc. is recalling 40 bags of Heparin 1,000 Units in NS 250mL due to potential leakage that compromises sterility.

    Product
    HEPARIN 1,000 Units in NS 250mL. (Heparin Sodium, USP 1,000 Units, 0.9% Sodium Chloride, USP 250 mL) Volume: 251 mL. Single dose bag. For: Adventist Medical Center Hanford. By: Avella of Huston, 9265 Kirby Dr., Houston TX, 77054. NDC 42852-747-25
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2453-2018·2018-07-25

    Ethicon Prolene Suture Recall Due to Packaging Perforation Risk

    Ethicon is recalling specific Prolene suture products because a packaging design issue may allow needles to perforate the package, posing injury and infection risks.

    Product
    PROLENE SUTURE 36"(90CM) 4-0 BLUE, D7768
    Category
    Medical Device
    Distribution
    25 states
  • HighFDA (Devices)·Z-2491-2018·2018-07-25

    Cardinal Health Recalls Hydroline Trumpet Valves Due to Suction Defect

    Cardinal Health 200, LLC is recalling Hydroline Trumpet Valves because the suction valve may not close properly, potentially causing continuous suction.

    Product
    Hydroline Trumpet Valve, Trumpet Valve, 5mm x 33cm Probe, Double Spike, Ref ASU1201, packaged 1/box, 12 boxes/case, single use, RX, Sterile.
    Category
    Medical Device
    Distribution
    34 states
  • HighNHTSA·18E061000·2018-07-25

    Rock Run Recalls LP Bottle Ring Brackets for Propane Tank Safety

    Rock Run Industries is recalling LP Bottle Ring Brackets that may break, potentially causing propane cylinders to fall from vehicles.

    Product
    EQUIPMENT:RECREATIONAL VEHICLE/TRAILER:LPG SYSTEMS:TANK ASSEMBLY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2490-2018·2018-07-25

    Cardinal Health Recalls Hydroline Trumpet Valves Due to Suction Defect

    Cardinal Health 200, LLC is recalling Hydroline Trumpet Valves because the suction valve may not close properly, potentially causing continuous suction.

    Product
    Hydroline Trumpet Valve, Trumpet Valve, 5mm x 33cm Probe, Single Spike, Ref ASU1200, packaged 1/box, 12 boxes/case, single use, RX, Sterile.
    Category
    Medical Device
    Distribution
    34 states
  • HighFDA (Devices)·Z-2459-2018·2018-07-25

    Ethicon Recalls Certain Prolene Sutures Due to Packaging Design Issue

    Ethicon, Inc. is recalling specific Prolene suture products because a packaging design issue allows the needle to perforate the package, posing a risk of injury or infection.

    Product
    PROLENE SUTURE 36"(90CM) 4-0 BLUE, D9067
    Category
    Medical Device
    Distribution
    25 states
  • HighFDA (Drugs)·D-0949-2018·2018-07-25

    Avella Recalls Hydromorphone Syringes Due to Sterility Concerns

    Avella of Deer Valley is recalling 480 single-dose hydromorphone syringes due to potential bag leakage and lack of sterility assurance.

    Product
    HYDROmorphone 1 mg/mL (HYDROmorphone HCL (USP) 30 mg, 0.9% Sodium Chloride (USP) QS 30 mL) Volume: 30mL. Single dose syringe. Avella of Houston, 9265 Kirby Dr., Houston, TX. NDC 42852-222-63
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2447-2018·2018-07-25

    NewDeal TIBIAXYS Medical Device Recalled Due to Infection Risk

    NewDeal SA is recalling TIBIAXYS devices because use may cause superficial or deep infections requiring antibiotic treatment or device removal.

    Product
    TIBIAXYS, Model Numbers: 150010S, 150020S, 150030S, 150040S, 150120S, 150110S, 150130S, 150200S, 150240S, 150242S, 150246S, 150250S, 150255S, 150260S, 150265S, 150270S, 150275S, 150280S, 150285S, 150290S, 150514S & 150516S
    Category
    Medical Device
    Distribution
    19 states
  • HighFDA (Devices)·Z-2452-2018·2018-07-25

    Ethicon Recalls Certain Proline Sutures Due to Packaging Design Issue

    Ethicon is recalling specific Proline sutures because a packaging design issue allows the needle to perforate the package, posing a risk of injury or infection.

    Product
    PROLENE SUTURE 30"(75CM) 4-0 BLUE, D7748
    Category
    Medical Device
    Distribution
    25 states
  • HighFDA (Food)·F-1651-2018·2018-07-25

    TR Toppers Chopped Chocolate Pretzel Pieces Recalled for Peanut Contamination

    T R Toppers, Inc. is recalling Chopped Chocolate Pretzel Pieces due to potential peanut contamination. Consumers should check for Lot 10481 and stop using the product.

    Product
    TR Toppers Brand Chopped Chocolate Pretzel Pieces. Item number B160-075 GTIN 0 06 51844 10599 6, 7.5 Lbs. (3 x 2.5 Lbs. Bags), Best Kept Between 34¿F and 40¿F <50% Relative Humidity
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2486-2018·2018-07-25

    Cardinal Health Recalls Hydroline Trumpet Valves Due to Suction Defect

    Cardinal Health 200, LLC is recalling Hydroline Trumpet Valves because the suction valve may not close properly, potentially causing continuous suction.

    Product
    Hydroline Trumpet Valve with Pulse Wave Cassette, Trumpet Valve with Cassette, 5mm x 33cm Composite Probe, Single Spike, Ref ASC1200, packaged 1/box, 12 boxes/case, single use, RX, Sterile.
    Category
    Medical Device
    Distribution
    34 states
  • HighFDA (Devices)·Z-2432-2018·2018-07-25

    Medtronic Vectris MRI Lead Kit Recalled for Needle Defect

    Medtronic is voluntarily recalling Vectris Sure Scan MRI Lead Kits because a manufacturing defect in the curved tip introducer needle may cause difficulty advancing or withdrawing the lead.

    Product
    Vectris(TM) Sure Scan(R) MRI Lead Kit for Spinal Cord Stimulation, Models: (a) 977A160 (b) 977A175 (c) 977A190 (d) 977A260 (e) 977A275 (f) 977A290 Product Usage: The Medtronic Vectris lead kits contain the implantable spinal cord stimulation lead, as well as additional co
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2433-2018·2018-07-25

    AesDex Cardica C-Port xA PLUS Anastomosis System Recalled for Handle Damage

    AesDex is recalling 587 Cardica C-Port xA PLUS Anastomosis Systems because the handle mechanism may break during use, causing a loud noise and potential dispersion of plastic fragments.

    Product
    AesDex, LLC Cardica C-Port xA PLUS Anastomosis System. Catalog Number FG-000100. The Cardica C-Port xA PLUS Anastomosis System, delivers a series of clips that create an anastomosis between a small target vessel (e.g. coronary artery) and conduit (e.g. saphenous vein graft)
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2460-2018·2018-07-25

    Ethicon Recalls Proline Sutures Due to Packaging Perforation Risk

    Ethicon is recalling specific Proline sutures because the needle may perforate the packaging, posing a risk of soft tissue injury or infection.

    Product
    PROLENE SUTURE 4"(10CM) 8-0 BLUE, D9662
    Category
    Medical Device
    Distribution
    25 states
  • HighFDA (Devices)·Z-2466-2018·2018-07-25

    Ethicon Recalls Pronova Suture Due to Packaging Perforation Risk

    Ethicon is recalling 516 units of Pronova Suture Blue because the needle may perforate the packaging, posing a risk of soft tissue injury or infection.

    Product
    PRONOVA SUTURE BLUE 122CM M1.5, D10189
    Category
    Medical Device
    Distribution
    25 states
  • HighFDA (Devices)·Z-2461-2018·2018-07-25

    Ethicon Recalls Certain Prolene Sutures Due to Packaging Perforation Risk

    Ethicon is recalling specific Prolene suture products because a packaging design issue may allow needles to perforate the package, posing injury and infection risks.

    Product
    PROLENE SUTURE BLUE 48" 4-0 D/A SH-1, D9746
    Category
    Medical Device
    Distribution
    25 states
  • HighFDA (Devices)·Z-2437-2018·2018-07-25

    Siemens Dimension Vista MULTI 1 SDIL Diluent Recall for Defective Septum

    Siemens is recalling 197 units of Dimension Vista MULTI 1 SDIL diluent due to a potential defect in the vial cap septum that may cause inaccurate test results.

    Product
    Dimension Vista¿ MULTI 1 SDIL, KD693, SMN# 10469971
    Category
    Medical Device
    Distribution
    53 states
  • HighFDA (Devices)·Z-2464-2018·2018-07-25

    Ethicon Recalls Proline Sutures Due to Packaging Perforation Risk

    Ethicon is recalling 372 units of Proline Suture Blue 18" 7-0 because the needle may perforate the packaging, posing a risk of soft tissue injury or infection.

    Product
    PROLENE SUTURE BLUE 18" 7-0 D/A BV-1, DC631
    Category
    Medical Device
    Distribution
    25 states
  • HighFDA (Devices)·Z-2507-2018·2018-07-25

    Medtronic Tri-Staple 2.0 Reloads Recalled for Missing Sled Component

    Medtronic is recalling Tri-Staple 2.0 Black Intelligent Reloads because a missing sled component may prevent staple formation, potentially causing bleeding or leakage.

    Product
    Tri-Staple 2.0 Black Intelligent Reload for use with Signia stapling system 60 mm Extra Thick, Item Code SIG60AXT
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2454-2018·2018-07-25

    Ethicon Recalls Proline Sutures Due to Packaging Perforation Risk

    Ethicon is recalling 588 units of Proline Suture Blue 4x18" 5/0 due to a packaging design issue that may allow the needle to perforate the package, posing a risk of injury or infection.

    Product
    PROLENE SUTURE BLUE 4X18"5/0 DA RB-2 +PLG, D7879
    Category
    Medical Device
    Distribution
    25 states
  • HighFDA (Devices)·Z-2456-2018·2018-07-25

    Ethicon Recalls Proline Sutures Due to Packaging Perforation Risk

    Ethicon is recalling 300 units of Proline Suture 30" 6-0 Blue because a packaging design issue may allow the needle to perforate the package, posing injury or infection risks.

    Product
    PROLENE SUTURE 30"(75CM) 6-0 BLUE, D8647
    Category
    Medical Device
    Distribution
    25 states
  • HighFDA (Devices)·Z-2493-2018·2018-07-25

    Cardinal Health Recalls Hydroline Trumpet Valves Due to Suction Defect

    Cardinal Health is recalling Hydroline Trumpet Valves because the suction valve may not close properly, potentially causing continuous suction.

    Product
    Hydroline Trumpet Valve, Trumpet Valve, 5mm x 28cm Probe, Double Spike, Ref ASU1211, packaged 1/box, 12 boxes/case, single use, RX, Sterile. Manufactured For Cardinal Health, Waukegan, IL.
    Category
    Medical Device
    Distribution
    34 states
  • HighFDA (Devices)·Z-2462-2018·2018-07-25

    Ethicon Recalls Certain Prolene Sutures Due to Packaging Perforation Risk

    Ethicon is recalling specific Prolene suture products because a packaging design issue allows needles to perforate the package, posing risks of soft tissue injury or infection.

    Product
    PROLENE SUTURE 36"(90CM) 3-0 BLU, D9844
    Category
    Medical Device
    Distribution
    25 states
  • HighFDA (Devices)·Z-2450-2018·2018-07-25

    Ethicon Recalls Certain Prolene Sutures Due to Packaging Design Issue

    Ethicon is recalling specific Prolene suture products because a packaging design issue allows needles to perforate the package, posing a risk of injury or infection.

    Product
    PROLENE SUTURE 4-36"(90CM) 4-0 BLUE, D5988
    Category
    Medical Device
    Distribution
    25 states
  • HighFDA (Devices)·Z-2316-2018·2018-07-25

    Wescam MX-10 Surveillance Laser System Recalled for Ocular Hazard

    Wescam Inc is recalling 29 MX-10 surveillance laser systems because the ocular hazard distance is longer than specified, posing a risk of eye exposure.

    Product
    MX-10 surveillance laser system Product Usage: The expected usage of the product is to facilitate observation and surveillance missions from safe standoff ranges.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0942-2018·2018-07-25

    Avella Recalls Ropivacaine Infusion Bags Due to Sterility Concerns

    Avella of Deer Valley, Inc. is recalling 20 bags of 0.2% Ropivacaine infusion cassettes due to potential leakage that compromises sterility.

    Product
    0.2% ROPivacaine, (Ropivacaine HCL PF, USP 500mg, 0.9% Sodium Chloride, USP QS 250 mL). Volume 250 mL. Single dose Cassette. For: Parkland Memorial Hospital. By: Advanced Pharma, 9225 Kirby Dr. Houston, TX 77054. Parkland Memorial Hospital NDC 15082-002-87
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2457-2018·2018-07-25

    Ethicon Recalls Prolene Sutures Due to Packaging Perforation Risk

    Ethicon is recalling specific Prolene suture units because a packaging design issue allows needles to perforate the package, posing injury and infection risks.

    Product
    PROLENE SUTURE 24"(60CM) 6-0 BLUE, D8688
    Category
    Medical Device
    Distribution
    25 states
  • HighFDA (Devices)·Z-2455-2018·2018-07-25

    Ethicon Recalls Certain Prolene Sutures Due to Packaging Design Issue

    Ethicon, Inc. is recalling 432 units of Prolene Suture 30" 8-0 Blue (D8292) because the needle may perforate the packaging, posing a risk of injury or infection.

    Product
    PROLENE SUTURE 30"(75CM) 8-0 BLUE, D8292
    Category
    Medical Device
    Distribution
    25 states
  • HighFDA (Devices)·Z-2494-2018·2018-07-25

    Cardinal Health Recalls Hydroline Trumpet Valves Due to Suction Defect

    Cardinal Health is recalling Hydroline Trumpet Valves because the suction valve may not close properly, potentially causing continuous suction.

    Product
    Hydroline Trumpet Valve, Trumpet Valve, No Probe, Single Spike, Ref ASU1220, packaged 1/box, 12 boxes/case, single use, RX, Sterile.
    Category
    Medical Device
    Distribution
    34 states
  • HighFDA (Devices)·Z-2458-2018·2018-07-25

    Ethicon Recalls Proline Sutures Due to Packaging Perforation Risk

    Ethicon is recalling specific Proline sutures because a packaging design issue allows needles to perforate the package, posing injury and infection risks.

    Product
    PROLENE SUTURE 24"(60CM) 7-0 BLUE, D8881
    Category
    Medical Device
    Distribution
    25 states
  • HighFDA (Devices)·Z-2448-2018·2018-07-25

    Ethicon Recalls Proline Sutures Due to Packaging Perforation Risk

    Ethicon is recalling specific Proline suture products because a packaging design issue allows needles to perforate the package, posing injury and infection risks.

    Product
    PROLENE SUTURE MONO BLUE - BV1755 Taper Point 3/8C, D10031
    Category
    Medical Device
    Distribution
    25 states
  • HighFDA (Devices)·Z-2471-2018·2018-07-25

    Tandem t:slim G4 Insulin Pump Recalled for Inaccurate Battery Readings

    Tandem Diabetes Care is recalling 55 t:slim G4 Insulin Pumps because the fuel gauge may provide inaccurate battery readings, causing the pump to stop delivering insulin.

    Product
    t:slim G4 Insulin Pump with Dexcom G4 Platinum CGM Software version: 4.3.4.3, Firmware version: 004722, Firmware, Fuel Gauge, Binary Rev B.
    Category
    Medical Device
    Distribution
    23 states
  • HighFDA (Devices)·Z-2487-2018·2018-07-25

    Cardinal Health Recalls Hydroline Trumpet Valves Due to Suction Defect

    Cardinal Health is recalling Hydroline Trumpet Valves because the suction valve may not close properly, potentially causing continuous suction.

    Product
    Hydroline Trumpet Valve with Pulse Wave Cassette, Trumpet Valve with Cassette, 5mm x 33cm Composite Probe, Double Spike, Ref ASC1201, packaged 1/box, 12 boxes/case, single use, RX, Sterile.
    Category
    Medical Device
    Distribution
    34 states
  • HighFDA (Devices)·Z-2492-2018·2018-07-25

    Cardinal Health Recalls Hydroline Trumpet Valves Due to Suction Defect

    Cardinal Health 200, LLC is recalling Hydroline Trumpet Valves because the suction valve may not close properly, potentially causing continuous suction.

    Product
    Hydroline Trumpet Valve, Trumpet Valve, 5mm x 28cm Probe, Single Spike, Ref ASU1210, packaged 1/box, 12 boxes/case, single use, RX, Sterile. .
    Category
    Medical Device
    Distribution
    34 states
  • HighFDA (Devices)·Z-2501-2018·2018-07-25

    Medtronic Recalls Visualase Cooled Laser Applicator Systems Due to Calibration Issues

    Medtronic is recalling 1,283 Visualase Cooled Laser Applicator Systems because calibration errors may cause low laser energy output or fiber burnout.

    Product
    Visualase Cooled Laser Applicator System (VCLAS) labeled as: a. Part Number 9735559, Visualase¿ Cooled Laser Applicator System 3mm Tip; b. Part Number 9735560 Visualase¿ Cooled Laser Applicator System 10mm Tip; c. Part Number 9735561 Visualase¿ Cooled Laser Applicator
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2488-2018·2018-07-25

    Cardinal Health Recalls Hydroline Trumpet Valves Due to Suction Defect

    Cardinal Health is recalling Hydroline Trumpet Valves because the suction valve may not close properly, potentially causing continuous suction.

    Product
    Hydroline Trumpet Valve with Pulse Wave Cassette, Trumpet Valve with Single Spike and no Probe, Ref ASC1220, packaged 1/box, 12 boxes/case, single use, RX, Sterile.
    Category
    Medical Device
    Distribution
    34 states
  • HighFDA (Devices)·Z-2451-2018·2018-07-25

    Ethicon Recalls Certain Prolene Sutures Due to Packaging Design Issue

    Ethicon, Inc. is recalling specific Prolene suture products because a packaging design issue allows the needle to perforate the package, posing a risk of injury or infection.

    Product
    PROLENE SUTURE 4-36" (90CM) 3-0 BLUE, D6416
    Category
    Medical Device
    Distribution
    25 states
  • HighFDA (Devices)·Z-2449-2018·2018-07-25

    Ethicon Proline Suture Recall Due to Packaging Perforation Risk

    Ethicon is recalling 1,728 units of Proline suture because a packaging design issue allows needles to perforate the package, posing injury and infection risks.

    Product
    PROLENE SUTURE BLUE 4X90CM M1.5 USP 4/0 DA RB-1 +P, D5981
    Category
    Medical Device
    Distribution
    25 states
  • HighFDA (Devices)·Z-2495-2018·2018-07-25

    Cardinal Health Recalls Hydroline Trumpet Valves Due to Suction Defect

    Cardinal Health is recalling Hydroline Trumpet Valves because the suction valve may not close properly, potentially causing continuous suction.

    Product
    Hydroline Trumpet Valve, Trumpet Valve, No Probe, Double Spike, Ref ASU1221, packaged 1/box, 12 boxes/case, single use, RX, Sterile.
    Category
    Medical Device
    Distribution
    34 states
  • HighFDA (Drugs)·D-0944-2018·2018-07-25

    Avella Recalls Fentanyl and Bupivacaine Cassettes Due to Sterility Concerns

    Avella of Deer Valley, Inc. is recalling 15 cassettes of fentanyl and bupivacaine due to potential bag leakage and lack of sterility assurance.

    Product
    fentaNYL 3 mcg/mL, 0.1% Bupivacaine, Fentanyl Citrate, USP 750 mcg, Bupivacaine HCL PF, USP, 250 mg, 0.9% Sodium Chloride, USP QS 250 mL. Volume: 250mL. Single dose Cassette. For: Methodist St. John Hospital, By: Advanced Pharma, 9265 Kirby Dr., Houston, TX 77054. NDC 15082-250-8
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1663-2018·2018-07-25

    Naked Bread Hamburger Buns Recalled for Undeclared Milk Allergen

    United States Bakery Corp is recalling Naked Bread Hamburger Buns due to undeclared milk. Consumers should stop eating the product.

    Product
    Naked Bread Hamburger Buns #NothingToHide, 8 pack. Product is packaged in low density polyethylene bag and identified as Naked Bread Hamburger Buns #NothingToHide, Net wt. 16.5 oz., UPC #72220 11075. The label is read in parts: "***INGREDIENTS: ENRICHED UNBLEACHED WHEAT FL
    Category
    Food
    Distribution
    6 states
  • ModerateFDA (Devices)·Z-2469-2018·2018-07-25

    Fx Solutions Offset Heads Recalled for Blister Breach

    Fx Solutions is recalling specific lots of Humelock Offset Heads due to a breach in the external blister packaging.

    Product
    Fx SOLUTIONS OFFSET HEAD CoCr 50x20, REF 106-5000 Product Usage: Device is designed to produce and deliver proton beam for the treatment of patients with localized tumors and other conditions susceptible to treatment by radiation. The PTS may include a fixed small beam treatm
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2482-2018·2018-07-25

    Cardinal Health Recalls Presource PBDS Kits Due to Leaking Gatorade Pouches

    Cardinal Health is recalling Presource PBDS kits because a defect in the Gatorade pouch seal caused the pouch to leak within the kit.

    Product
    Presource PBDS, Kit, No Spiro. Kit includes a exerciser volumetric 5000 ML device, two items of cloth, skin prep 2% CHG, a packet of 4 chlorhexidine gluconate antiseptic cloths, and Gatorade pouches. Product Usage: The kit is provided to a patient pre-surgery, as part of the
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2436-2018·2018-07-25

    Siemens Dimension Vista CTNI Sample Diluent Recalled for Defective Cap Septum

    Siemens Healthcare Diagnostics is recalling 1,446 units of Dimension Vista CTNI Sample Diluent because a defective cap septum may cause erroneously elevated test results.

    Product
    Dimension Vista¿ CTNI Sample Diluent, KD692, SMN# 10445205
    Category
    Medical Device
    Distribution
    53 states
  • ModerateFDA (Devices)·Z-2430-2018·2018-07-25

    Valeris Medical Recalls Apollo XT Suture Anchors Due to Material Mislabeling

    Valeris Medical is recalling 113 Apollo XT Suture Anchors because the labels incorrectly identified the material as titanium instead of PEEK.

    Product
    Apollo XT Suture Anchor, 5.5 x 15 Product Usage: Apollo XT Suture Anchors are intended for: Shoulder - Rotator Cuff Repair - Bankart Repair - SLAP Lesion Repair - Biceps Tenodesis - Acromio-Clavicular Separation Repair - Deltoid Repair - Capisular Shift or Capsulolabral Recon
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2431-2018·2018-07-25

    Medtronic Vectris Trial Screening Lead Kit Recalled for Needle Defect

    Medtronic is voluntarily recalling Vectris Trial Screening Lead Kits because a manufacturing defect in the curved tip introducer needle may cause difficulty advancing or withdrawing the lead.

    Product
    Vectris(TM) Trial Screening Lead Kit for Spinal Cord Stimulation, Models: (a) 977D160 (b) 977D260 Product Usage: The Medtronic Vectris lead kits contain the implantable spinal cord stimulation lead, as well as additional components used for lead implant as part of a Neurost
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-2483-2018·2018-07-25

    Cardinal Health Recalls Presource PBDS Kits Due to Leaking Gatorade Pouches

    Cardinal Health is recalling 8,928 Presource PBDS kits because a defect in the Gatorade pouch seal caused the pouch to leak within the kit.

    Product
    Presource PBDS, Kit, No Spiro Diabetes. Kit includes a exerciser volumetric 5000 ML device, two items of cloth, skin prep 2% CHG, a packet of 4 chlorhexidine gluconate antiseptic cloths, and Gatorade pouches. Product Usage: The kit is provided to a patient pre-surgery, as pa
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2438-2018·2018-07-25

    Siemens Dimension Vista MULTI 2 SDIL Diluent Recall for Defective Septum

    Siemens is recalling 1,195 units of Dimension Vista MULTI 2 SDIL diluent because a defective septum may cause erroneously elevated test results.

    Product
    Dimension Vista¿ MULTI 2 SDIL, KD694, SMN# 10483586
    Category
    Medical Device
    Distribution
    53 states
  • ModerateFDA (Drugs)·D-0924-2018·2018-07-25

    Sun Pharmaceutical Recalls Metformin Hydrochloride Tablets Due to Foreign Matter

    Sun Pharmaceutical Industries is recalling one lot of Metformin Hydrochloride Extended Release Tablets because a piece of rubber glove was detected in a tablet.

    Product
    METFORMIN HYDROCHLORIDE — METFORMIN HYDROCHLORIDE (METFORMIN HYDROCHLORIDE)
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-2439-2018·2018-07-25

    Opgen Recalls AdvanDx QuickFISH Slides Due to Diminished Performance

    Opgen Inc is recalling AdvanDx QuickFISH Slides because they may show diminished performance before their expiration date.

    Product
    AdvanDx QuickFISH Slides, a component of the QuickFish BC Fixation Kit - BC, REF QFFIXBC1-25, Catalog Number: CS012 Control slides included as a component of the QFFIXBC1-25. The slides will provide non-fluorescent, wettable surface with dimensions appropriate for testing samp
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2480-2018·2018-07-25

    Cardinal Health Recalls Presource PBDS Kits Due to Leaking Gatorade Pouches

    Cardinal Health is recalling 8,928 Presource PBDS kits because a defect in the Gatorade pouch seal caused the pouch to leak within the kit.

    Product
    Presource PBDS, Kit, Common Diabetes. Kit includes a exerciser volumetric 5000 ML device, two items of cloth, skin prep 2% CHG, a packet of 4 chlorhexidine gluconate antiseptic cloths, and Gatorade pouches. Product Usage: The kit is provided to a patient pre-surgery, as part
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2481-2018·2018-07-25

    Cardinal Health Recalls Presource PBDS Kits Due to Gatorade Pouch Seal Defect

    Cardinal Health is recalling 8,928 Presource PBDS kits because a defect in the Gatorade pouch seal caused the pouch to leak within the kit.

    Product
    Presource PBDS, Kit, Common. Kit includes a exerciser volumetric 5000 ML device, two items of cloth, skin prep 2% CHG, a packet of 4 chlorhexidine gluconate antiseptic cloths, and Gatorade pouches. Product Usage: The kit is provided to a patient pre-surgery, as part of the
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2484-2018·2018-07-25

    Stryker Recalls Reprocessed Harmonic Ace Shears Due to Error Code

    Stryker is recalling 180 reprocessed Harmonic Ace shears because they may display an error code preventing use.

    Product
    Reprocessed HARMONIC Ace¿ +7, 5mm Diameter Shears with Advanced Hemostasis (HARH), Item Number HARH36 Product Usage: The Reprocessed HARMONIC ACE¿+7, 5 mm Diameter Shears with Advanced Hemostasis are indicated for soft tissue incisions when bleeding control and minimal therma
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2440-2018·2018-07-25

    Canadian Hospital Specialties Recalls Pediatric Feeding Tubes with Incorrect Length Labeling

    Canadian Hospital Specialties is recalling specific lots of pediatric feeding tubes because they may be packaged with the incorrect length as labeled.

    Product
    MED-RX, Ref 54-1650R 5Fr X 16 inch (40cm) Polyurethane Feeding Tube For Pediatric Use with Orange Radiopaque Stripe and Enteral Connector, packaged 10/case, Sterile, RX. The firm name on the label is chs, Oakville, ON, Canada.
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-2442-2018·2018-07-25

    Health Harmony Mobile App Recalled for Data Synchronization Delays

    Intel-GE Care Innovations LLC is recalling the Health Harmony Mobile application because patient data sometimes failed to sync with the backend database in a timely manner.

    Product
    Health Harmony Mobile application software Product Usage: Care Innovations Health Harmony Mobile is intended as a communication tool to display medical device data from third party devices for patients to view, and to collect assessment (question &#38; answers) from patients
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2468-2018·2018-07-25

    Fx Solutions Proton Beam Therapy Heads Recalled for Blister Breach

    Fx Solutions is recalling specific proton beam therapy heads due to a breach in the external blister packaging.

    Product
    Fx SOLUTIONS CENTERED HEAD CoCr 50x19, REF 106-5019 Product Usage: Device is designed to produce and deliver proton beam for the treatment of patients with localized tumors and other conditions susceptible to treatment by radiation. The PTS may include a fixed small beam trea
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0920-2018·2018-07-25

    Hain Celestial Recalls alba BOTANICA Sunscreen Due to Incorrect Formulation

    The Hain Celestial Group is recalling alba BOTANICA sport mineral sunscreen because the wrong product formulation was placed in the packages.

    Product
    alba BOTANICA sport mineral sunscreen (titanium dioxide 7.0% and zinc oxide 9.0%), spf 45, 170 g (6 oz) tubes packaged in a) 4 tubes per case; b) 8 pack shipper display; Manufactured By: The Hain Celestial Group, Inc., Lake Success, NY 11042, UPC 7 24742 01102 4.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2496-2018·2018-07-25

    Philips Ingenuity Digital PET/CT System Recall for Pallet Assembly Defect

    Philips is recalling 32 Ingenuity Digital PET/CT Systems because a block connecting the patient pallet to the couch may be assembled incorrectly, potentially causing a misaligned screw.

    Product
    Ingenuity Digital PET/CT System, Model 882446 with the following UDI's: (01)00884838059559(21)900004 (01)00884838059559(21)900005 (01)00884838059559(21)900006 (01)00884838059559(21)900007 (01)00884838059559(21)900008 (01)00884838059559(21)900009 (01)00884838059559(21)9000
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2435-2018·2018-07-25

    Edwards SAPIEN 3 Transcatheter Heart Valve Recalled for Incorrect Size Labeling

    Edwards Lifesciences is recalling one SAPIEN 3 Transcatheter Heart Valve because it was packaged with the incorrect valve size relative to the label.

    Product
    Edwards SAPIEN 3 Transcatheter Heart Valve (THV), Model: 9600TFX, Size: 26 mm
    Category
    Medical Device
    Distribution
    1 state
  • SevereNHTSA·18E060000·2018-07-24

    SynTec Recalls School Bus Seats Due to Mounting Foot Defect

    SynTec is recalling S3B 45-inch Restraint School Bus Seats because the mounting foot may pull through the bolted joint at the bus floor, increasing injury risk in a crash.

    Product
    SEATS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·18190·2018-07-24

    Ross Stores Recalls Bistro Chairs Due to Frame Breakage and Fall Hazard

    Ross Stores is recalling Bronze Hammered bistro chairs because the frames can break, posing a fall hazard. Consumers should stop using the chairs and return them for a full refund.

    Product
    Bistro chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·18192·2018-07-24

    JCPenney Recalls Okie Dokie Shorts Due to Choking Hazard

    JCPenney is recalling Okie Dokie Denim Patches Shortie shorts because the patches can detach, posing a choking hazard to young children.

    Product
    Okie Dokie Denim Patches Shortie shorts
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·18V488000·2018-07-23

    Karma Revero Recalled for Non-Compliant Driver Side Rearview Mirror Glass

    Karma Automotive is recalling 2018 Revero vehicles because the driver's side exterior rearview mirror may use convex glass instead of flat glass, failing federal safety standards.

    Product
    KARMA — KARMA REVERO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V489000·2018-07-20

    BraunAbility Recalls Wheelchair Vans Due to Brake Line Connection Defect

    Braun Corporation is recalling 2012-2018 BraunAbility Dodge and Chrysler wheelchair vans because brake lines may be disconnected, reducing electronic stability control performance.

    Product
    BRAUNABILITY — BRAUNABILITY DODGE WHEELCHAIR VAN, CHRYSLER WHEELCHAIR VAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18E059000·2018-07-20

    Jost Recalls Fifth Wheel Assemblies Due to Narrow Bracket Risk

    Jost International is recalling certain Outboard Sliders because a narrow bracket may allow the trailer to separate from the tractor, increasing crash risk.

    Product
    TRAILER HITCHES:FIFTH WHEEL ASSEMBLY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V487000·2018-07-20

    Freightliner Recalls M2 Trucks for Steering Shaft Installation Defect

    Daimler Trucks is recalling 2018-2019 Freightliner Business Class M2 trucks because an incorrectly installed steering shaft may disconnect the steering wheel from the front wheels.

    Product
    FREIGHTLINER — FREIGHTLINER BUSINESS CLASS M2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18E058000·2018-07-20

    Meritor Recalls Wheel Studs Due to Potential Heat Treatment Defect

    Meritor is recalling specific wheel studs installed in steer axle hubs because improper heat treatment may cause them to fail, potentially leading to wheel detachment.

    Product
    WHEELS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V472000·2018-07-20

    Van-Con Recalls School Buses Due to Seat Foam Crash Protection Defect

    Van-Con is recalling 2011-2018 33803 Dual Rear Wheel school buses because seat foam may not absorb enough impact in a crash, increasing injury risk.

    Product
    VAN-CON — VAN-CON 33803 DUAL REAR-WHEEL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·pha-07202018-1·2018-07-20

    FSIS Public Health Alert for Hungry Man Dinners with Recalled Whey Powder

    The USDA FSIS issued a public health alert for Hungry Man frozen dinners containing whey powder recalled due to possible Salmonella contamination. No adverse reactions have been reported.

    Product
    FSIS Issues Public Health Alert For Products Containing FDA-Regulated Whey Powder That Has Been Recalled Due To Possible Salmonella Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V480000·2018-07-19

    Ducati Recalls 2018 Motorcycles Due to Rear Brake Pad Defect

    Ducati is recalling 2018 Panigale and Hypermotard motorcycles because rear brake pad friction material may detach, increasing stopping distance and crash risk.

    Product
    DUCATI — DUCATI PANIGALE V4, HYPERMOTARD, PANIGALE 959, PANIGALE 1299 FE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V482000·2018-07-19

    Thor Outlaw Motorhomes Recalled for Missing Rear Reflectors

    Thor Motor Coach is recalling 2018-2019 Outlaw motorhomes because they lack required rear reflex reflectors, which reduces visibility to other drivers.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH OUTLAW
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1009-2018·2018-07-18

    Gaia Kratom Powder Recalled for Salmonella Contamination

    Gaia Ethnobotanical LLC is recalling specific lots of Gaia Kratom powder due to FDA-confirmed Salmonella contamination.

    Product
    Gaia Kratom (mitragyna speciosa) powder, Red Kapuas Hulu , 1oz, 250g, 1kg packages, Gaia Ethnobotanical.com
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1000-2018·2018-07-18

    Gaia Kratom Powder Recalled for Salmonella Contamination

    Gaia Ethnobotanical LLC is recalling Gaia Kratom powder due to FDA-confirmed Salmonella contamination. Consumers should stop using the product.

    Product
    Gaia Kratom (mitragyna speciosa) powder, Green MD, 1oz, 250g, 1kg packages, Gaia Ethnobotanical.com
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·064-2018·2018-07-18

    Win Opportunity Knocks Recalls Raw Ground Beef for E. coli Contamination

    Win Opportunity Knocks is recalling approximately 6,020 pounds of fresh and frozen raw ground beef products due to possible contamination with Shiga toxin-producing E. coli.

    Product
    Win Opportunity Knocks Recalls Fresh and Frozen, Raw Ground Beef Products Due to Possible E. coli O45, O103 and O145 Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1007-2018·2018-07-18

    Gaia Kratom Powder Recalled for Salmonella Contamination

    Gaia Ethnobotanical LLC is recalling Red Dragon Kratom powder due to Salmonella contamination found by FDA analysis.

    Product
    Gaia Kratom (mitragyna speciosa) powder, Red Dragon, 1oz, 250g, 1kg packages, Gaia Ethnobotanical.com
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0998-2018·2018-07-18

    Gaia Kratom Powder Recalled for Salmonella Contamination

    Gaia Ethnobotanical LLC is recalling Gaia Kratom powder due to FDA analysis confirming Salmonella contamination.

    Product
    Gaia Kratom (mitragyna speciosa) powder, Green Kapuas Hulu, 1oz, 250g, 1kg packages, Gaia Ethnobotanical.com
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1010-2018·2018-07-18

    Gaia Kratom Powder Recalled for Salmonella Contamination

    Gaia Ethnobotanical LLC is recalling Gaia Kratom powder due to FDA-confirmed Salmonella contamination.

    Product
    Gaia Kratom (mitragyna speciosa) powder, Red MD, 1oz, 250g, 1kg packages, Gaia Ethnobotanical.com
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0995-2018·2018-07-18

    Gaia Kratom Powder Recalled for Salmonella Contamination

    Gaia Ethnobotanical LLC is recalling Gaia Kratom powder due to FDA analysis confirming salmonella contamination.

    Product
    Gaia Kratom (mitragyna speciosa) powder, Ganesh, 1oz, 250g, 1kg packages, Gaia Ethnobotanical.com
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1005-2018·2018-07-18

    Gaia Kratom Powder Recalled for Salmonella Contamination

    Gaia Ethnobotanical LLC is recalling various Gaia Kratom powder products nationwide due to FDA-confirmed Salmonella contamination.

    Product
    Gaia Kratom (mitragyna speciosa) powder, Red Bali, 1oz, 250g, 1kg packages, Gaia Ethnobotanical.com Gaia Ethnobotanical Red Borneo, 1oz, 250g, kg Gaia Ethnobotanical Red Dragon, 1oz, 250g, 1kg Gaia Ethnobotanical Red Horn, 1oz, 250g, 1kg Gaia Ethnobotanical Red Kapua
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0997-2018·2018-07-18

    Gaia Kratom Powder Recalled for Salmonella Contamination

    Gaia Ethnobotanical LLC is recalling specific lots of Gaia Kratom powder due to FDA-confirmed Salmonella contamination.

    Product
    Gaia Kratom (mitragyna speciosa) powder, Green Horn, 1oz, 250g, 1kg packages, Gaia Ethnobotanical.com
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1004-2018·2018-07-18

    Gaia Kratom Powder Recalled for Salmonella Contamination

    Gaia Ethnobotanical LLC is recalling Gaia Kratom powder due to FDA-confirmed Salmonella contamination.

    Product
    Gaia Kratom (mitragyna speciosa) powder, Purple 8-1, 1oz, 250g, 1kg packages, Gaia Ethnobotanical.com
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1016-2018·2018-07-18

    Gaia Kratom Powder Recalled for Salmonella Contamination

    Gaia Ethnobotanical LLC is recalling Gaia Kratom powder due to FDA-confirmed Salmonella contamination.

    Product
    Gaia Kratom (mitragyna speciosa) powder, Yellow Vietnam, 1oz, 250g, 1kg packages, Gaia Ethnobotanical.com
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0999-2018·2018-07-18

    Gaia Kratom Powder Recalled for Salmonella Contamination

    Gaia Ethnobotanical LLC is recalling Green Malay Kratom powder due to FDA-confirmed Salmonella contamination.

    Product
    Gaia Kratom (mitragyna speciosa) powder, Green Malay, 1oz, 250g, 1kg packages, Gaia Ethnobotanical.com
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1653-2018·2018-07-18

    Peanut Processors Recalls Dry Roasted Peanut Meal Due to Salmonella

    Peanut Processors, Inc. is recalling 30 lb boxes of Dry Roasted Peanut Meal after a customer reported the product tested positive for Salmonella.

    Product
    DRY ROASTED PEANUT MEAL NET WT 30LBS Peanut Processors of Sherman Hwy 87 & Albert Street, Dublin, NC 28332
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Drugs)·D-0996-2018·2018-07-18

    Gaia Kratom Powder Recalled for Salmonella Contamination

    Gaia Ethnobotanical LLC is recalling Green Dragon Kratom powder due to FDA-confirmed Salmonella contamination.

    Product
    Gaia Kratom (mitragyna speciosa) powder, Green Dragon, 1oz, 250g, 1kg packages, Gaia Ethnobotanical.com
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0993-2018·2018-07-18

    Gaia Kratom Powder Recalled for Salmonella Contamination

    Gaia Ethnobotanical LLC is recalling Gaia Kratom powder due to FDA-confirmed Salmonella contamination.

    Product
    Gaia Kratom (mitragyna speciosa) powder, Bali Gold, 1oz, 250g 1kg packages, Gaia Ethnobotanical.com
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1008-2018·2018-07-18

    Gaia Kratom Powder Recalled for Salmonella Contamination

    Gaia Ethnobotanical LLC is recalling Gaia Kratom powder due to FDA-confirmed Salmonella contamination. Consumers should stop using the product.

    Product
    Gaia Kratom (mitragyna speciosa) powder, Red Horn, 1oz, 250g, 1kg packages, Gaia Ethnobotanical.com
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1001-2018·2018-07-18

    Gaia Kratom Powder Recalled for Salmonella Contamination

    Gaia Ethnobotanical LLC is recalling Gaia Kratom powder due to FDA-confirmed Salmonella contamination.

    Product
    Gaia Kratom (mitragyna speciosa) powder, Green Thai, 1oz, 250g, 1kg packages, Gaia Ethnobotanical.com
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1654-2018·2018-07-18

    Honey Mama's Peppermint Cacao Bar Recalled for Undeclared Almonds

    Nectar Foods LLC is recalling Honey Mama's Oregon Peppermint Cacao-Nectar Bars due to undeclared almonds, a major food allergen.

    Product
    Honey Mama's Oregon Peppermint Cacao-Nectar Bar wrapped in quilon parchment paper with a sticker label. Net wt. 2.5 oz, 3" x 3" bar, 12 bars to a cardboard display case and 12 display cases to a cardboard master case. UPC on each bar is 8 54835 00402 9. The product label is re
    Category
    Food
    Distribution
    18 states
  • CriticalFDA (Drugs)·D-1006-2018·2018-07-18

    Gaia Kratom Powder Recalled for Salmonella Contamination

    Gaia Ethnobotanical LLC is recalling Gaia Kratom powder due to FDA-confirmed Salmonella contamination.

    Product
    Gaia Kratom (mitragyna speciosa) powder, Red Borneo, 1oz, 250g, 1kg packages, Gaia Ethnobotanical.com
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1002-2018·2018-07-18

    Gaia Kratom Powder Recalled for Salmonella Contamination

    Gaia Ethnobotanical LLC is recalling Gaia Kratom powder due to FDA-confirmed Salmonella contamination.

    Product
    Gaia Kratom (mitragyna speciosa) powder, Plantation Red MD, 1oz, 250g, 1kg packages, Gaia Ethnobotanical.com
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1013-2018·2018-07-18

    Gaia Kratom Powder Recalled for Salmonella Contamination

    Gaia Ethnobotanical LLC is recalling Gaia Kratom powder due to FDA-confirmed Salmonella contamination. Consumers should stop using the product.

    Product
    Gaia Kratom (mitragyna speciosa) powder, White MD, 1oz, 250g, 1kg packages, Gaia Ethnobotanical.com
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1003-2018·2018-07-18

    Gaia Kratom Powder Recalled for Salmonella Contamination

    Gaia Ethnobotanical LLC is recalling Gaia Kratom powder due to FDA analysis confirming Salmonella contamination.

    Product
    Gaia Kratom (mitragyna speciosa) powder, Plantation White MD, 1oz, 250g, 1kg packages, Gaia Ethnobotanical.com
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1652-2018·2018-07-18

    Peanut Processors Recalls Dry Roasted Peanut Granules Due to Salmonella

    Peanut Processors, Inc. is recalling dry roasted peanut granules after a customer reported the product tested positive for Salmonella.

    Product
    DRY ROASTED MEDIUM CHOP PEANUT GRANULES NET WT 30LBS (13.61 KGS) Peanut Processors of Sherman Hwy 87 & Albert Street, Dublin, NC 28332
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Drugs)·D-1012-2018·2018-07-18

    Gaia Kratom Powder Recalled for Salmonella Contamination

    Gaia Ethnobotanical LLC is recalling Gaia Kratom powder due to FDA-confirmed Salmonella contamination.

    Product
    Gaia Kratom (mitragyna speciosa) powder, White Horn, 1oz, 250g, 1kg packages, Gaia Ethnobotanical.com
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0994-2018·2018-07-18

    Gaia Kratom Powder Recalled for Salmonella Contamination

    Gaia Ethnobotanical LLC is recalling specific lots of Gaia Kratom powder due to FDA-confirmed Salmonella contamination.

    Product
    Gaia Kratom (mitragyna speciosa) powder, Elephant, 1oz, 250g, 1kg packages, Gaia Ethnobotanical.com
    Category
    Food
    Distribution
    Distributed nationwide

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