The Recall Desk

Archive

May 2017 recalls

771 recalls were announced in May 2017.

What the numbers show

Critical
45
Severe
174
High
254
Moderate
259
Low
39

Of the 771 recalls this month scored against our rubric, 6% are Critical, 23% are Severe.

301–400 of 771

  • ModerateFDA (Food)·F-2234-2017·2017-05-24

    Kemps Recalls Sweet Me Creamery Ice Cream and Frozen Yogurt for Plastic

    Kemps, LLC is recalling select pints of Sweet Me Creamery Ice Cream and YO2 Frozen Yogurt because they may contain pieces of plastic.

    Product
    Kemps Sweet Me Creamery Maple Toffee Blondie, One Pint, UPC 41483-04146
    Category
    Food
    Distribution
    20 states
  • ModerateFDA (Devices)·Z-2075-2017·2017-05-24

    Zimmer CAS Recalls Navitrack System Knee Instrument Due to Software Anomalies

    Zimmer CAS is voluntarily recalling 152 units of the Navitrack System - OS Knee Universal due to software anomalies corrected in a new revision.

    Product
    Navitrack¿ System - OS Knee Universal, Orthopedic Stereotaxic Instrument
    Category
    Medical Device
    Distribution
    20 states
  • ModerateFDA (Food)·F-2239-2017·2017-05-24

    Herbalife Recalls Peanut Butter Protein Bars Due to Fish Gelatin

    Herbalife is recalling Peanut Butter Protein Bars because they may contain trace amounts of fish gelatin, an undeclared allergen.

    Product
    Protein Bar 14 bars/box, Net Wt. 19.74oz (560g) Each shipping carton contains 12 boxes
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2102-2017·2017-05-24

    Medical Action Industries Recalls Blue OR Towels Due to Lint Presence

    Medical Action Industries is recalling specific lots of Blue OR Towels because lint was found on the sterile towels.

    Product
    Blue OR Towels, X-Ray Detectable, Sterile, 2 Towels per/pk; 48pk/Cs and 4 Towels per/pk; (20pk/Cs). Intended for packing and absorption externally or within patient wounds in various procedures or surgical cases.
    Category
    Medical Device
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-2082-2017·2017-05-24

    Beckman Coulter Recalls HDL Cholesterol Reagent Due to Drug Interference

    Beckman Coulter is recalling HDL Cholesterol Reagent because specific drugs can cause false low results.

    Product
    HDL Cholesterol Reagent (HDL 2 x 200), Catalog No. A15625. Intended for quantitative determination of HDL cholesterol in the high density lipoprotein fraction of human serum or plasma.
    Category
    Medical Device
    Distribution
    1 state
  • ModerateUSDA FSIS·054-2017·2017-05-24

    Armour Eckrich Recalls Sausage Due to Possible Metal Contamination

    Armour Eckrich Meats is recalling approximately 90,978 pounds of ready-to-eat sausage products that may contain pieces of metal. No adverse reactions have been reported.

    Product
    Armour Eckrich Meats, LLC Recalls Ready-To-Eat Sausage Products Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    6 states
  • ModerateFDA (Devices)·Z-2090-2017·2017-05-24

    Hitachi Arietta 70 Ultrasound System Recalled for Weak Arm Mounting Mechanism

    Hitachi Medical Systems America Inc is recalling 77 Arietta 70 Ultrasound Systems because the arm mounting mechanism was insufficiently strong and required redesign.

    Product
    Arietta 70 Ultrasound System Intended for use by trained personnel (doctor, sonographer. etc.) for the diagnostic Ultrasound evaluation.
    Category
    Medical Device
    Distribution
    18 states
  • ModerateFDA (Devices)·Z-2080-2017·2017-05-24

    Beckman Coulter Recalls Enzymatic Creatinine Reagent Due to Interference

    Beckman Coulter is recalling Enzymatic Creatinine Reagent because specific drugs can cause false low results. The recall affects 12,665 units distributed worldwide.

    Product
    Enzymatic Creatinine Reagent (CR-E 2 x 200), Catalog No. A60298. Intended for the quantitative determination of creatinine (CR-E) concentration in human serum, plasma or urine.
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-2073-2017·2017-05-24

    Biomet Microfixation Recalls Surgical Trays Due to Part Number Mismatch

    Biomet Microfixation is recalling 33 TraumaOne System Surgical Trays because the part number on the lid differs from the base.

    Product
    Biomet Microfixation TraumaOne System Surgical Tray - Model # 46-1600
    Category
    Medical Device
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-2104-2017·2017-05-24

    Medline Recalls Distraction Pins Due to Potential Sterility Loss

    Medline Industries is recalling 2,112 packs of sterile distraction pins because the packaging seal may be compromised, risking loss of sterility.

    Product
    16 mm [or 18 mm] Distraction Pin, Qty: 1 per pack; STERILE; Manufactured for: Medline Industries, Inc., Mundelein, IL 60060 USA Distraction Pin is designed for Anterior Cervical Fusion Procedures. Use with vertebral body distraction instruments. It is intended as a temporary fix
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1893-2017·2017-05-24

    Ziehm Imaging solo FD Mobile Fluoroscopic C-arm Recalled for Missing Label Date

    Ziehm Imaging Inc is recalling two solo FD Mobile Fluoroscopic C-arm systems because the labels for the Collimator and X-ray Control panel are missing the manufacturer date.

    Product
    Ziehm Imaging solo FD Mobile Fluoroscopic C-arm
    Category
    Medical Device
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-2081-2017·2017-05-24

    Beckman Coulter Cholesterol Reagent Recalled for Potential Drug Interference

    Beckman Coulter is recalling Cholesterol Reagent (Catalog No. 467825) because specific drugs may cause false low results.

    Product
    Cholesterol Reagent(CHOL 2 x 300), Catalog No. 467825 Intended for quantitative determination of cholesterol concentration in human serum or plasma.
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-2101-2017·2017-05-24

    Medical Action Industries Recalls Sterile Operating Room Towels Due to Lint

    Medical Action Industries is recalling sterile operating room towels because lint is present on the product.

    Product
    White OR Towels, X-Ray Detectable, Sterile, 4 Towels per/pk; 20pk/Cs. Intended for packing and absorption externally or within patient wounds in various procedures or surgical cases.
    Category
    Medical Device
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-2083-2017·2017-05-24

    Beckman Coulter Recalls Triglycerides Reagent Due to Interference

    Beckman Coulter is recalling Triglycerides Reagent because specific drugs can cause false low results.

    Product
    Triglycerides Reagent (TG 2 x 300), Catalog No. 445850. Intended for quantitative determination of triglycerides concentration in human serum or plasma.
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0790-2017·2017-05-24

    Taro Recalls Fluocinonide Cream Due to Hydrocortisone Contamination

    Taro Pharmaceuticals is recalling specific lots of Fluocinonide Cream 0.05% due to cross-contamination with hydrocortisone-17-valerate.

    Product
    FLUOCINONIDE — FLUOCINONIDE (FLUOCINONIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2108-2017·2017-05-24

    Teleflex Recalls Visistat Skin Staplers Due to Labeling Error

    Teleflex Medical is recalling Visistat 35R Disposable Skin Staplers because some boxes are mislabeled as containing Wide devices when they contain Regular devices.

    Product
    WECK Visistat 35R Disposable Skin Stapler, Ref 528135, Rx Only, Sterile EO, Visistat is indicated for the external skin closure of lacerations on the outer layer of the dermis for a wide range of general, thoracic, obstetric, gynecological, orthopedic, cardiovascular, urologic
    Category
    Medical Device
    Distribution
    20 states
  • ModerateFDA (Devices)·Z-2078-2017·2017-05-24

    Beckman Coulter Recalls Lactate Reagent Due to Interference from Specific Drugs

    Beckman Coulter is recalling Lactate Reagent (Catalog No. A95550) because certain drugs can cause false low results.

    Product
    Lactate Reagent (LACT 2 x 50), Catalog No. A95550 Intended for the quantitative determination of Lactate concentration in human plasma and cerebrospinal fluid (CSF).
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-2076-2017·2017-05-24

    Zimmer CAS Recalls Navitrack System OS Knee Universal Software

    Zimmer CAS is voluntarily recalling Navitrack System OS Knee Universal software versions due to software issues causing errors and discrepancies.

    Product
    Navitrack System - OS Knee Universal, Stereotaxic instrument
    Category
    Medical Device
    Distribution
    16 states
  • ModerateFDA (Devices)·Z-2085-2017·2017-05-24

    Siemens Recalls Insulin Calibrators Due to Measurement Deviation

    Siemens Healthcare Diagnostics is recalling ADVIA Centaur Systems Insulin Calibrators because they measure approximately 40% higher than the WHO standard.

    Product
    ADVIA Centaur Systems Insulin Calibrator; Test Code: Calibrator IRI; Catalog Number: 04618899
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-2079-2017·2017-05-24

    Beckman Coulter Recalls Uric Acid Reagent Due to Drug Interference

    Beckman Coulter is recalling Uric Acid Reagent because certain drugs can cause false low results. The recall covers 100,286 units distributed worldwide.

    Product
    Uric Acid Reagent (URIC 2 x 300), Catalog No. 442785. Intended for the quantitative determination of uric acid concentration in human serum, plasma or urine.
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-2107-2017·2017-05-24

    Medline 12 mm Distraction Pin Recalled for Potential Sterility Loss

    Medline Industries is recalling 300 packs of 12 mm Distraction Pins because the sterile packaging seal may be compromised, potentially allowing the device to lose sterility.

    Product
    12 mm Distraction Pin, Blunt Qty: 1 per pack; STERILE; Manufactured for: Medline Industries, Inc., Mundelein, IL 60060 USA Distraction Pin is designed for Anterior Cervical Fusion Procedures. Use with vertebral body distraction instruments. It is intended as a temporary fixation
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2224-2017·2017-05-24

    Kemps Recalls Frozen Yogurt and Ice Cream Due to Plastic Contamination

    Kemps is recalling select pints of Sweet Me Creamery Ice Cream and YO2 Frozen Yogurt because they may contain pieces of plastic.

    Product
    Kemps YO2 Frozen Yogurt Salty Caramel Cookie Crunch, One Pint, UPC 41483-04123
    Category
    Food
    Distribution
    20 states
  • LowFDA (Devices)·Z-2096-2017·2017-05-24

    Abbott AMO Vitrectomy Cutters Recalled for Packaging Error

    Abbott Medical Optics is recalling 360 AMO Vitrectomy Cutters because 20GA and 25GA models may be packaged in the wrong sizes.

    Product
    AMO 25GA Vitrectomy Cutter (Model Number NGP0025) and AMO 20GA Vitrectomy Cutter and Irrigation Sleeve (Model Number NGP0020) Used with the AMO Whitestar Signature System. For ophthalmic use.
    Category
    Medical Device
    Distribution
    0 states
  • LowFDA (Devices)·Z-2116-2017·2017-05-24

    Medtest Holdings Recalls Pointe Scientific Hitachi AST Reagent Due to Labeling Discrepancy

    Medtest Holdings is recalling Pointe Scientific Hitachi AST Reagent because the package insert contains inconsistent linearity values in different sections.

    Product
    Pointe Scientific Hitachi AST Reagent R1 : PE plastic bottle w/PP plastic cap. R2: PE plastic bottle w /PP plastic cap. Product Usage: Two Part Chemistry Reagent For the quantitative determination of Aspartate Aminotransferase (ASl) in human serum on Hitachi analyzers.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0787-2017·2017-05-24

    Teligent Recalls Desoximetasone Ointment Due to Superpotent Drug Classification

    Teligent, Inc. is voluntarily recalling 3,600 tubes of Desoximetasone Ointment 0.25% in Tennessee due to a superpotent drug classification.

    Product
    Desoximetasone Ointment USP, 0.25%, 15 g tubes, Rx Only, Teligent Pharma, Inc. Buena. New Jersey 08310 NDC 52565-030-15
    Category
    Drug
    Distribution
    1 state
  • HighCPSC·17162·2017-05-23

    Dynacraft Recalls Ride-On Toys Due to Sticking Pedal Hazard

    Dynacraft is recalling about 20,000 Surge and Tonka battery-operated ride-on toys because the acceleration pedal can stick, posing fall and crash hazards.

    Product
    Surge and Tonka battery operated ride-on toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·17164·2017-05-23

    Pier 1 Imports Recalls Temani Wicker Furniture for Lead Paint Violation

    Pier 1 Imports is recalling Temani wicker chairs, settees, and ottomans because the paint may contain excessive lead, violating federal standards.

    Product
    Temani ivory wicker chair, settee and ottoman
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·17V334000·2017-05-23

    REV Road Rescue Emergency Vehicles Recalled for Cot Securing Bolt Defect

    REV is recalling 24 Road Rescue emergency vehicles because short bolts may fail to secure the cot during a crash, potentially injuring occupants.

    Product
    ROAD RESCUE — ROAD RESCUE TYPE IX, TYPE I, TYPE III
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17166·2017-05-23

    Hobby Lobby Recalls Easter and July 4th Light-Up Spinner Toys

    Hobby Lobby is recalling Easter and July 4th-themed light-up spinner toys because the battery cover can detach, exposing coin cell batteries that pose choking and ingestion hazards to young children.

    Product
    Easter and July 4th-themed Light-Up Spinner Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·17T010000·2017-05-23

    Kenda Kenetica Tires Recalled for Steel Belt Void Risk

    American Kenda Rubber Industrial is recalling specific Kenetica tires due to a void in the steel belt that may cause tread separation or sudden air loss.

    Product
    TIRES recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V335000·2017-05-23

    Keystone Recalls 2017-2018 Dutchmen Voltage Trailers Due to Fuel Line Defect

    Keystone RV Company is recalling 2017-2018 Dutchmen Voltage trailers with Onan 5.5 generators because an incorrectly clamped fuel line may disconnect, causing a fuel leak and fire risk.

    Product
    DUTCHMEN — DUTCHMEN VOLTAGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V332000·2017-05-22

    Ford Recalls 2017 Models for Manual Seat Recliner Weld Defect

    Ford is recalling 2017 Explorer and F-Series trucks because manual seat back recliners may have inadequate welds, increasing injury risk in a crash.

    Product
    FORD — FORD EXPLORER, F-150, F-550 SD, F-350 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V331000·2017-05-22

    Ford Recalls 2015-2017 F-Series Trucks for Door Handle Cover Defect

    Ford is recalling specific 2015-2017 F-Series trucks equipped with chrome door handle covers that may cause doors to unlatch in a side impact, increasing injury risk.

    Product
    FORD — FORD F-150, redundant F-350, redundant F-250, F-550
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V333000·2017-05-22

    Harley-Davidson Recalls 2017 Motorcycles Due to Oil Cooler Line Clamp Defect

    Harley-Davidson is recalling 45,589 2017 motorcycles because an improperly installed clamp may cause the engine oil cooler line to detach, increasing crash risk.

    Product
    HARLEY-DAVIDSON — HARLEY-DAVIDSON FLHTCU, FLTRX, FLHTP, FLHRXS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·pha-051617-exp·2017-05-20

    Imported Veal Products Recalled Over Possible E. coli O103 Contamination

    USDA FSIS issued a Public Health Alert for approximately 1,631 pounds of raw veal products imported from the Netherlands due to possible contamination with Non-O157 Shiga toxin-producing E. coli O103. No illnesses have been reported.

    Product
    FSIS Issues Public Health Alert For Imported Veal Products Due To Possible Non-O157 Shiga toxin producing E. coli (STEC) O103 Contamination
    Category
    Food
    Distribution
    4 states
  • CriticalCPSC·17159·2017-05-19

    Blomberg and Summit Electric Ranges Recalled for Electrocution Hazard

    Arçelik A.S. is recalling about 6,300 Blomberg and Summit electric ranges because they can become energized, posing shock and electrocution risks.

    Product
    Blomberg and Summit electric ranges
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V330000·2017-05-19

    Columbia Aliner Ascape Trailers Recalled for Loose Propane Gas Trays

    Columbia Northwest is recalling 2017-2018 Aliner Ascape trailers because liquid propane gas bottle trays may detach, increasing the risk of fire or crash.

    Product
    COLUMBIA — COLUMBIA ALINER ASCAPE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateUSDA FSIS·052-2017·2017-05-19

    John Morrell Recalls Beef Franks Due to Possible Metal Contamination

    John Morrell and Co. is recalling approximately 210,606 pounds of beef frank products due to possible metal contamination. No injuries have been reported.

    Product
    John Morrell and Co. Recalls Beef Frank Products Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·051-2017·2017-05-18

    Osso Good Co. Recalls Beef and Pork Bone Broth Products

    The Osso Good Co. is recalling approximately 1,210 pounds of beef and pork bone broth products produced without federal inspection.

    Product
    Yosemite Protein Products, Inc. — The Osso Good Co. Recalls Beef and Pork Products Produced Without Benefit of Inspection
    Category
    Food
    Distribution
    5 states
  • SevereNHTSA·17V328000·2017-05-18

    BMW Recalls 2005-2008 7 Series Vehicles for Door Latch Defect

    BMW is recalling 2005-2008 7 Series and B7 Alpina vehicles because doors may appear latched but can unexpectedly open, risking occupant ejection.

    Product
    BMW — BMW 745I, 760LI, 750LI, 760I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V326000·2017-05-18

    Ferrara Recalls Fire Apparatus Due to Guardrail Defect

    Ferrara is recalling 2000-2016 Fire Apparatus 100' Platform vehicles because a movable ladder access guardrail may bend or break under heavy loads, increasing injury risk.

    Product
    FERRARA — FERRARA APPARATUS 100' PLATFORM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17157·2017-05-18

    Michaels Recalls Ceramic Travel Mugs Due to Burn Hazard

    Michaels is recalling Celebrate It ceramic travel mugs because the lids do not fit securely, creating a risk of burns from leaking hot liquids.

    Product
    Ceramic travel mugs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·17156·2017-05-18

    Pier 1 Imports Recalls Chalk Note Mugs Due to Burn Hazard

    Pier 1 Imports is recalling Chalk Note Mugs because they can crack when filled with hot liquid, posing a burn hazard to users.

    Product
    Chalk Note Mugs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • LowNHTSA·17V327000·2017-05-18

    BMW Recalls 2017 X5 M and X6 M for Incorrect Tire Labeling

    BMW is recalling 2017 X5 M and X6 M vehicles because the tire information label lists the wrong tire size, failing to meet federal safety standards.

    Product
    BMW — BMW X6, X5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-2216-2017·2017-05-17

    Frito-Lay Recalls Miss Vickies Multipacks Due to Potential Salmonella

    Frito-Lay is recalling 32-count Miss Vickies Multipacks due to potential Salmonella contamination. The recall covers units distributed nationwide and in Puerto Rico.

    Product
    32 count Miss Vickies Multipack Box 44 oz. packaged in flexible plastic
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-2215-2017·2017-05-17

    Frito-Lay Recalls Lays Kettle Cooked Multipacks Due to Salmonella Risk

    Frito-Lay is recalling 1,196,880 units of Lays Kettle Cooked Multipack Trays nationwide due to the potential presence of Salmonella.

    Product
    30 count Lays Kettle Cooked Multipack Tray 41.25 oz. packaged in flexible plastic
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-2213-2017·2017-05-17

    Frito-Lay Bold Mix Sack Recalled for Potential Salmonella Presence

    Frito-Lay is recalling 20-count Bold Mix Sacks nationwide due to the potential presence of Salmonella.

    Product
    20 count Frito-Lay Bold Mix Sack 18.4 oz. packaged in flexible plastic
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2205-2017·2017-05-17

    Hummingbird Wholesale Recalls Organic Cocoa-Dusted Chocolate Ginger for Undeclared Hazelnuts

    Hummingbird Wholesale is recalling Organic Cocoa-Dusted Chocolate Ginger due to undeclared hazelnuts. The product was distributed in Oregon in 5 lb. bags and bulk bins.

    Product
    Organic Cocoa-Dusted Chocolate Ginger, packaged and distributed in 5 lbs. bulk bag. Product was later offered to consumers in a self-serve bulk bin at retail store. The label is read in parts: "***Organic Cocoa-Dusted Chocolate Ginger***Made with Fair Trade 70% Dark Chocolate
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-2206-2017·2017-05-17

    Farming Fish Organic Basil Pesto Recalled for Listeria Risk

    Our Local Bounty is recalling Farming Fish brand Organic Basil Pesto with Watercress due to potential Listeria monocytogenes contamination.

    Product
    Farming Fish brand Organic Basil Pesto with Watercress, was packaged in 8.5 oz. plastic deli containers. UPC 7 23175 33586 8. The label is read in parts: "***100% Organic Basil Pesto with Watercress *** 8.5oz***Ingredients: ALL ORGANIC Basil, Watercress, Sunflower Seed Oil, Su
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-2211-2017·2017-05-17

    Frito-Lay Recalls Jalapeño Flavored Potato Chips Due to Salmonella Risk

    Frito-Lay is recalling Jalapeño Flavored Lays Kettle Cooked and Miss Vickies Kettle Cooked potato chips due to a potential presence of Salmonella.

    Product
    Jalape¿o Flavored Lays Kettle Cooked potato chips and Jalape¿o Flavored Miss Vickies Kettle Cooked potato chips in the following unit sizes: 1.75 oz, 2.75 oz, 8 oz, 13.5 oz, 2.125 oz, 6.5 oz, 0.85 oz, 1.375 oz, 2.25 oz, and 1.375 oz
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2212-2017·2017-05-17

    Frito-Lay Recalls Lays Kettle Cooked Multipacks Due to Salmonella Risk

    Frito-Lay is recalling 12-count Lays Kettle Cooked Multipacks nationwide due to potential Salmonella presence.

    Product
    12 count Lays Kettle Cooked Multipack Sack 10.2 oz packaged in flexible plastic
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2068-2017·2017-05-17

    Zimmer Biomet Recalls Regenerex Patella Implants Due to Peg Shearing

    Zimmer Biomet is recalling 8,154 Regenerex Series A Patella implants because the pegs may shear after surgery.

    Product
    Regenerex Patella RGX 3 PEG SER A PATELLA 28MM RGX 3 PEG SER A PATELLA 31MM RGX 3 PEG SER A PATELLA 34MM RGX 3 PEG SER A PATELLA 37MM Product Usage: The Regenerex Series A Patella can be used for any non-cemented resurfaced 3-peg patella application within the Vanguard Co
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2204-2017·2017-05-17

    Del Monte Caesar Side Salad Recalled for Undeclared Allergens

    Del Monte is recalling 7-Eleven Caesar Side Salads sold in Colorado due to undeclared milk, eggs, wheat, and fish.

    Product
    7-ELEVEN CAESAR SIDE SALAD 3 oz. packaged in clear plastic container
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Devices)·Z-2042-2017·2017-05-17

    Arthrex Recalls Anthrex PEEK SwiveLock SP Vented Anchors Due to Breakage

    Arthrex, Inc. is recalling specific Anthrex PEEK SwiveLock SP Vented anchors because some eyelets broke during insertion. The recall covers units distributed in the US and several international locations.

    Product
    Anthrex PEEK SwiveLock SP Vented, 5.5mm x 24.5 mm, Self-Punching
    Category
    Medical Device
    Distribution
    49 states
  • SevereFDA (Food)·F-2184-2017·2017-05-17

    Rosa Foods Recalls Soylent Powder for Undeclared Milk Allergen

    Rosa Foods is recalling Soylent 1.8 Powder because it may contain undeclared milk (whey). Consumers should stop using the product.

    Product
    Soylent 1.8 Powder , 7 x 15oz pouches, SKU: 1WK-V108
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Devices)·Z-2045-2017·2017-05-17

    Arthrex SpeedBridge Implant System Recalled for Broken Eyelets

    Arthrex is recalling specific SpeedBridge Implant Systems because some eyelets broke during insertion. The recall covers multiple batches distributed in the US and internationally.

    Product
    Anthrex SpeedBridge Implant System with BioComposite SwiveLock SP Vented, 5.5 mm x 24 mm
    Category
    Medical Device
    Distribution
    49 states
  • SevereNHTSA·17V324000·2017-05-17

    Isuzu Recalls NPR and GMC Trucks Due to Stuck Accelerator Pedal

    Isuzu is recalling certain 2008-2009 and 2012-2013 NPR, NPR HD, and GMC W3500/W4500 trucks because the throttle pedal may get stuck, causing high speeds and crash risk.

    Product
    ISUZU — ISUZU, CHEVROLET, GMC NPR, W3500, W4500, NPR HD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2050-2017·2017-05-17

    Mederi Stretta Catheter Recalled Due to Sterility Compromise

    Mederi Therapeutics is recalling 1,458 Stretta Catheter kits because a breach in the sterile barrier package compromised sterility.

    Product
    Mederi Stretta Catheter and Accessory Kit, Sterile For Use with the MEDERI MDRF1 GENERATOR ONLY. Used in the treatment of gastroesophageal reflux disease (GERD). REF 175-5580
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2060-2017·2017-05-17

    Savaria SL-1000 Stairlift Recalled Due to Fire Hazard

    Savaria Concord Lifts is recalling SL-1000 stairlifts because a defect in the electrical controller and motor can cause a fire.

    Product
    Savaria SL-1000 Stairlift
    Category
    Consumer Product
    Distribution
    0 states
  • HighFDA (Devices)·Z-2055-2017·2017-05-17

    Greatbatch Medical Recalls Linear Straight Broach Handles Due to Weld Breakage

    Greatbatch Medical is recalling specific Linear Straight Broach Handles because they may break at the welds or lose the locating pin during use.

    Product
    Linear Straight Broach Handle (Rasp Handle) (Greatbatch Part # 510397; DJO Surgical Inc., # 803-03-159) and EZ Clean" Linear Broach Handle Greatbatch Part # T11824, DJO Surgical Inc. # 803-03-059).
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Devices)·Z-2065-2017·2017-05-17

    Abbott Recalls Healon 5 Pro Due to Possible Glass Particles

    Abbott Medical Optics is recalling Healon 5 Pro ophthalmic solution because some units may contain microscopic glass particles from manufacturing damage.

    Product
    Healon 5 Pro, Part No. 10270015
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-2185-2017·2017-05-17

    Unisea Recalls Frozen Wild Shrimp Burgers Due to Allergen Labeling Error

    Unisea Inc. is recalling Wild Grill Foods brand frozen shrimp burgers because the packaging failed to list butter as an ingredient in the allergen declaration.

    Product
    Frozen Wild Shrimp Burgers, Wild Grill Foods brand, net wt. 12 oz. Each package contains 4/ 3 oz. pieces. UPC 8 94067 00248 6. The 12 oz. package label is read in parts: "***SHRIMP BURGERS***WILD GRILL***Net WT WT. 12 OZ.***Distributed by Wild Grill Foods***INGREDIENTS: Shrim
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-2191-2017·2017-05-17

    Givaudan Recalls Chipotle BBQ Seasoning Due to Potential Salmonella Contamination

    Givaudan Flavours Corp is recalling specific lots of SJ Chipotle BBQ seasoning because an ingredient may contain Salmonella. The product was distributed to Illinois, Ohio, and Missouri.

    Product
    SJ CHIPOLTE BBQ DB 36.7 lbs INGREDIENTS: SALT, SPICES INCLUDING Mustard***Wheat Flour***CONTAINS: SOY, WHEAT spicetec¿ FLAVORS & SEASONINGS 6 Santa Fe Way Cranbury, NJ 08512 (800) 345-7742
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-2062-2017·2017-05-17

    Abbott Recalls Healon Medical Device Due to Glass Particle Risk

    Abbott Medical Optics is recalling Healon medical devices because certain lots may contain microscopic glass particles from manufacturing damage.

    Product
    Healon, Part No. 10290953, 10295210, 10200011, 10200012, 10201012, 10203012, 10213012, 10223012, 10290701, 10294751, 10295701
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-2214-2017·2017-05-17

    Frito-Lay Recalls Miss Vickies Multipack Trays Due to Potential Salmonella

    Frito-Lay is recalling 30-count Miss Vickies Multipack Trays nationwide and in Puerto Rico due to the potential presence of Salmonella.

    Product
    30 count Miss Vickies Multipack Tray 41.25 oz. packaged in flexible plastic
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2203-2017·2017-05-17

    Reser's Macaroni Salad Recalled for Undeclared Milk and Soy Allergens

    Reser's Fine Foods is recalling American Classics Macaroni Salad because it contains undeclared milk and soy. The product was distributed to wholesalers in 12 states.

    Product
    Reser's Fine Foods, American Classics Macaroni Salad, Net Wt 1 lb. (454 g) UPC 7117.19007, packaged in 16 oz plastic tubs, 12 per case. Reser's Fine Foods, Inc. Beaverton, OR 97006.
    Category
    Food
    Distribution
    12 states
  • HighFDA (Food)·F-2201-2017·2017-05-17

    Farmo Foods Recalls Fresh Mozzarella Due to Metal Fragments

    Farmo Foods, Inc. is recalling 12,000 lbs of fresh mozzarella because metal fragments were found in the product.

    Product
    Fresh Mozzarella; No brand name. Shipped in 30 lb. plastic bucket
    Category
    Food
    Distribution
    1 state
  • HighNHTSA·17V325000·2017-05-17

    Bison Horse Trailers Recalled for Incorrect Weight Rating Labels

    Bison Coach is recalling 2016-2018 horse trailers due to incorrect Gross Axle Weight Rating labels, which may lead to overloading and increased crash risk.

    Product
    BISON — BISON TRAIL HAND, LAREDO, TRAIL BOSS, SILVERADO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2043-2017·2017-05-17

    Arthrex Bio Composite SwiveLock Anchor Eyelets Break on Insertion

    Arthrex is recalling specific batches of Bio Composite SwiveLock anchors because some eyelets broke during insertion.

    Product
    Anthrex Bio Composite SwiveLock SP Vented, 4.75 mm x 24.5 mm, Self-Punching
    Category
    Medical Device
    Distribution
    49 states
  • HighFDA (Food)·F-2188-2017·2017-05-17

    Frozen Pollock Mince Recalled Due to Metal Fragments

    GAS LLC is recalling frozen pollock mince blocks because a customer found metal fragments in the product.

    Product
    Pollock mince is frozen block, packed in waxed coated fiber block liners. Each frozen block weighs 7.45 KG. There are 3 blocks packaged in a fiber master carton that has a poly box liner. The master case is a brown carton with blue print that has the brand "Alaska Brands" on
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-2063-2017·2017-05-17

    Abbott Recalls Healon GV Due to Possible Microscopic Glass Particles

    Abbott Medical Optics is recalling Healon GV due to a remote possibility of microscopic glass particles from manufacturing damage.

    Product
    Healon GV, Part No. 10294701, 10294801, 10200014, 10201014, 10202014, 10203014
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2066-2017·2017-05-17

    Abbott Recalls Healon Pro Due to Possible Glass Particles

    Abbott Medical Optics is recalling Healon Pro ophthalmic solutions because manufacturing damage may have introduced microscopic glass particles.

    Product
    Healon Pro, Part No. 10270012
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-2200-2017·2017-05-17

    Pinnacle Foods Recalls Great Value Bread and Butter Chips for Glass Fragments

    Pinnacle Foods is recalling Great Value Bread and Butter Chips because glass fragments were found in the product. The chips were distributed nationwide.

    Product
    Great Value Bread and Butter Chips 24 Fl Oz. Distributed by: Wal-Mart Stores, Inc., Bentonville, AR 72716 UPC 078742145990
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2197-2017·2017-05-17

    Givaudan Recalls Spicetec Flavors and Seasonings Due to Salmonella Risk

    Givaudan Flavours Corp is recalling Spicetec Flavors & Seasonings because an ingredient may contain Salmonella. The product was shipped to Illinois, Ohio, and Missouri.

    Product
    SJ TABASCO Net Wgt: 36.33 LBS INGREDIENTS: Spices including Mustard, Salt, Paprika***Wheat Flour***CONTAINS: SOY, WHEAT spicetec¿ FLAVORS & SEASONINGS 6 Santa Fe Way Cranbury, NJ 08512 (800) 345-7742
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-2207-2017·2017-05-17

    Treehouse Foods Recalls Macaroni and Cheese Cups for Salmonella Risk

    Treehouse Foods is recalling specific brands of microwaveable macaroni and cheese cups because they may be contaminated with Salmonella.

    Product
    Macaroni & Cheese microwaveable cups sold under the following brands: 1. Big Win Original Macaroni & Cheese Dinner, UPC 11822-58403. 2. Cheese Club express mac Macaroni Cheese Dinner, UPC 41498-17167, 3. Great Value Macaroni & Cheese Dinner, UPC 78742-08249.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2195-2017·2017-05-17

    Givaudan Recalls Spicy Seasoning Mix Due to Salmonella Risk

    Givaudan Flavours Corp is recalling SJ SPICY DB seasoning mix because an ingredient may contain Salmonella. The product was shipped to Illinois, Ohio, and Missouri.

    Product
    SJ SPICY DB Net Wt. 48 LBS INGREDIENTS: Spices including Mustard, Paprika***Wheat Flour***CONTAINS: SOY, WHEAT spicetec¿ FLAVORS & SEASONINGS 6 Santa Fe Way Cranbury, NJ 08512 (800) 345-7742
    Category
    Food
    Distribution
    3 states
  • HighFDA (Drugs)·D-0705-2017·2017-05-17

    Teva Recalls Clozapine Tablets Due to Microbial Contamination

    Teva Pharmaceuticals is recalling specific lots of Clozapine Tablets USP, 25 mg, due to microbial contamination of non-sterile products.

    Product
    Clozapine Tablets USP, 25 mg, 100-count bottle (NDC 0093-4359-01), 500- count bottle (NDC 0093-4359-05), 100 Unit Dose Blisters per carton (NDC 0093-4359-93), Individual Blister Pack (NDC 0093-4359-19), Rx Only, Manufactured By: Teva Pharmaceutical Industries Ltd., Jerusalem, 977
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2041-2017·2017-05-17

    Arthrex Bio-SwiveLock SP Vented Anchor Recall Due to Broken Eyelets

    Arthrex, Inc. is recalling specific Bio-SwiveLock SP Vented anchors because some eyelets broke during insertion.

    Product
    Anthrex Bio-SwiveLock SP Vented, 5.5mm x 24.5 mm, Self-Punching
    Category
    Medical Device
    Distribution
    49 states
  • HighFDA (Devices)·Z-2046-2017·2017-05-17

    Arthrex Recalls Anthrex SpeedBridge Implant System Due to Broken Eyelets

    Arthrex, Inc. is recalling the Anthrex SpeedBridge Implant System because some eyelets broke from the SwiveLock Anchor during insertion.

    Product
    Anthrex SpeedBridge Implant System with PEEK SwiveLock Self Punching
    Category
    Medical Device
    Distribution
    49 states
  • HighFDA (Food)·F-2187-2017·2017-05-17

    Frozen Pollock Fillet Recalled Due to Metal Fragments

    GAS LLC is recalling frozen pollock fillet blocks because a customer found metal fragments in the product. The recall affects 6,848 cases distributed in Massachusetts and several countries.

    Product
    Pollock Fillet is frozen block, packed in waxed coated fiber block liners. Each frozen block weighs 7.45 KG. There are 3 blocks packaged in a fiber master carton that has a poly box liner. The master case is a brown carton with blue print that has the brand "Alaska Brands" o
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-2196-2017·2017-05-17

    Givaudan Recalls Sweet and Spicy Seasoning for Potential Salmonella

    Givaudan Flavours Corp is recalling 42.75 lb bags of SJ Sweet and Spicy seasoning because an ingredient may contain Salmonella.

    Product
    SJ SWEET AND SPICY Net Wt: 42.75 LBS INGREDIENTS: Brown Sugar, Spices including Mustard, Garlic Powder***Wheat Flour***CONTAINS: SOY, WHEAT spicetec¿ FLAVORS & SEASONINGS 6 Santa Fe Way Cranbury, NJ 08512 (800) 345-7742
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-2186-2017·2017-05-17

    Jimmy's Cookies Peanut Butter Chocolate Chunk Cookies Recalled for Undeclared Milk

    Jimmy's Cookies is recalling The Bakery Peanut Butter Chocolate Chunk Cookies because they may contain undeclared milk. The product was distributed nationwide.

    Product
    The Bakery Peanut Butter Chocolate Chunk Cookies, Net Wt. 14 oz. (396g), packaged in a clear plastic clam shell, UPC 0 78742 06652 3, Distributed by: Wal-Mart Stores, Inc. Bentonville, AR 72716
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2190-2017·2017-05-17

    Givaudan Recalls SJ Black Pepper Bags Due to Salmonella Risk

    Givaudan Flavours Corp is recalling 41 bags of SJ Black Pepper because an ingredient may contain Salmonella. The product was distributed to Illinois, Ohio, and Missouri.

    Product
    SJ Black Pepper 42.75 lbs INGREDIENTS: Black Pepper, Spices including Mustard, Paprika***Wheat Flour***CONTAINS: SOY, WHEAT spicetec¿ FLAVORS & SEASONINGS 6 Santa Fe Way Cranbury, NJ 08512 (800) 345-7742
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-2193-2017·2017-05-17

    Givaudan Recalls Spicetec Flavors and Seasonings Due to Salmonella Risk

    Givaudan Flavours Corp is recalling Spicetec Flavors & Seasonings because an ingredient may contain Salmonella. The product was shipped to Illinois, Ohio, and Missouri.

    Product
    SJ MILD DB 36.33 LBS INGREDIENTS: Salt,***Wheat Flour***CONTAINS: SOY, WHEAT spicetec¿ FLAVORS & SEASONINGS 6 Santa Fe Way Cranbury, NJ 08512 (800) 345-7742
    Category
    Food
    Distribution
    3 states
  • HighCPSC·17154·2017-05-17

    Cabrinha Recalls Kiteboard Control Systems Due to Injury and Fall Hazards

    Cabrinha is recalling about 2,900 kiteboard control systems because a stainless steel component can break, causing loss of kite control and posing injury and fall hazards.

    Product
    Cabrinha Kiteboard control systems
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2192-2017·2017-05-17

    Givaudan Recalls Spicetec Flavors Due to Potential Salmonella Contamination

    Givaudan Flavours Corp is recalling Spicetec Flavors & Seasonings because an ingredient may contain Salmonella. The product was shipped to Illinois, Ohio, and Missouri.

    Product
    SJ JALAPENO NACHO DB 42 LBS INGREDIENTS: Dextrose, Salt***Wheat Flour***CONTAINS: SOY, WHEAT spicetec¿ FLAVORS & SEASONINGS 6 Santa Fe Way Cranbury, NJ 08512 (800) 345-7742
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-2199-2017·2017-05-17

    Givaudan Recalls Brownie Mix Due to Potential Salmonella Contamination

    Givaudan Flavours Corp is recalling specific lots of SJ Dry Brownie Mix because an ingredient may contain Salmonella. The product was distributed to Illinois, Ohio, and Missouri.

    Product
    SJ DRY BROWNIE MIX 1003706 Net Wgt: 1200 LBS INGREDIENTS: Sugar, Wheat Flour, Cocoa Powder, Whole Egg Powder, Whey Powder, Sodium Bicarbonate. CONTAINS: MILK, WHEAT, EGG spicetec¿ FLAVORS & SEASONINGS 6 Santa Fe Way Cranbury, NJ 08512 (800) 345-7742
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-2198-2017·2017-05-17

    Givaudan Recalls SJ Taco Seasoning Due to Potential Salmonella Contamination

    Givaudan Flavours Corp is recalling 41 bags of SJ Taco seasoning because an ingredient may contain Salmonella. The product was distributed to Illinois, Ohio, and Missouri.

    Product
    SJ TACO Net Wgt: 44.5 LBS INGREDIENTS: Spices including Chili Pepper, Garlic Powder, Sugar, Paprika***Wheat Flour***CONTAINS: SOY, WHEAT spicetec¿ FLAVORS & SEASONINGS 6 Santa Fe Way Cranbury, NJ 08512 (800) 345-7742
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-2194-2017·2017-05-17

    Givaudan Recalls Philly Cheesesteak Seasoning Due to Salmonella Risk

    Givaudan Flavours Corp is recalling SJ Philly Cheesesteak Seasoning because an ingredient may contain Salmonella. The product was shipped to Illinois, Ohio, and Missouri.

    Product
    SJ PHILLY CHEESESTEAK SEASONING Net Wt: .44.5 LBS INGREDIENTS: Onion Powder, Green Bell Pepper Powder***Wheat Flour***CONTAINS: SOY, WHEAT spicetec¿ FLAVORS & SEASONINGS 6 Santa Fe Way Cranbury, NJ 08512 (800) 345-7742
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-2064-2017·2017-05-17

    Abbott Recalls Healon Duet Due to Potential Glass Particles

    Abbott Medical Optics is recalling Healon Duet units because they may contain microscopic glass particles from manufacturing damage.

    Product
    Healon Duet, Part No. 10290080, 10220010, 10220011 and 10220012
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2049-2017·2017-05-17

    Roche Diagnostics Recalls Sample Probes for Corrosion-Related Liquid Level Detection Issues

    Roche Diagnostics is recalling 3,946 sample probes for cobas analyzers because corrosion on electrical contacts can disrupt liquid level detection, potentially causing sample carryover.

    Product
    Sample probes associated with: cobas 6000 Series System, cobas 8000 Modular Analyzer Series, cobas c 311 analyzer cobas c 501/502 cobas c 701/702 cobas 8000 ISE Product Usage: The cobas 6000 series is a fully automated, random-access, software-controlled system for immun
    Category
    Medical Device
    Distribution
    Distributed nationwide

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