The Recall Desk

Archive

October 2016 recalls

1,035 recalls were announced in October 2016.

What the numbers show

Critical
136
Severe
242
High
453
Moderate
173
Low
31

Of the 1,035 recalls this month scored against our rubric, 13% are Critical, 23% are Severe.

501–600 of 1035

  • HighFDA (Food)·F-0062-2017·2016-10-19

    Gold Standard Baking Recalls Cheese Danish for Metal Shavings

    Gold Standard Baking is recalling The Bakery Cheese Danish sold at Walmart due to the presence of small metal shavings.

    Product
    The Bakery Cheese Danish | Net Wt 14 OZ (397g) | Distributed By WAL-MART Stores, Inc, Bentonville, AR 72716 | UPC: 605388124487
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0069-2017·2016-10-19

    Cardinal Health Recalls V. Mueller Spinal Distraction Screws Due to Corrosion

    Cardinal Health 200, LLC is recalling V. Mueller Neuro/Spine Shadow-Line Spinal Distraction Screws because corrosion was demonstrated on the screw surface.

    Product
    V. Mueller Neuro/Spine, SHADOW-LINE, SPINAL DISTRACTION SCREW, STERILE, various sizes (12mm, 14mm, 16mm and 18mm) 5 PER BOX.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0021-2017·2016-10-19

    Weis Markets Recalls Bakery Products Due to Potential Metal Fragments

    Weis Markets is voluntarily recalling 30 bakery products, including muffins and cookies, due to the potential presence of small metal fragments in the sugar topping.

    Product
    Monster Size Pina Colada Muffins (4 count)
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-0078-2017·2016-10-19

    R.W. Garcia Sweet Potato Crackers Recalled for Metal Fragments

    R.W. Garcia is recalling 3 Seed Sweet Potato Crackers because metal fragments were detected in the raw material.

    Product
    RW Garcia, 3 Seed, Sweet Potato Crackers, (Flaxseed, Sesame & Chia), Gluten Free, Net Wt., 30 oz., Product of USA, Manufactured & Distributed by R.W. Garcia Co., Inc., San Jose, CA 95112 and Lincolnton, NC 28092.
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-0085-2017·2016-10-19

    ConMed Recalls HeatWave Electrodes Due to Insulation Damage Risk

    ConMed is recalling specific HeatWave Electrodes because damaged shaft insulation could increase the risk of patient burns during arthroscopic procedures.

    Product
    CONCEPT HEATWAVE Electrode 130 mm x 2.3 mm diameter, REF/Catalog Number CS-023, STERILE, Rx Only Product Usage: The HeatWave Electrode is intended to be used for electro-coagulation of soft tissue in shoulder, ankle, wrist, elbow and knee arthroscopic procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0065-2017·2016-10-19

    Gold Standard Baking Recalls Apple Crumb Coffee Cake Due to Metal Shavings

    Gold Standard Baking is recalling The Bakery Apple Crumb Coffee Cake because it may contain small metal shavings.

    Product
    The Bakery Apple Crumb Coffee Cake| Net Wt 15 OZ (425g) | Distributed By WAL-MART Stores, Inc, Bentonville, AR 72716 | UPC: 078742052953
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·16V756000·2016-10-19

    Newmar Recalls 2017 King Aire Motorhomes Due to Radar Mounting Defect

    Newmar is recalling 2017 King Aire motorhomes because the collision mitigation radar may be mounted upside down, potentially decreasing performance and increasing crash risk.

    Product
    NEWMAR — NEWMAR KING AIRE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0053-2017·2016-10-19

    Publix Raspberry Strip Danish Recalled for Metal Shavings

    Gold Standard Baking is recalling Publix Raspberry Strip Danishes due to the presence of small metal shavings.

    Product
    Publix Raspberry Strip Danish | Count, 1 | NET WT 15.00 oz | Distributed by Publix Supermarkets, Inc., Lakeland, FL 33802
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0049-2017·2016-10-19

    Nature's Power Solutions Acidophilus Blend Recalled for Undeclared Milk

    Complete Packaging & Manufacturing is recalling Nature's Power Solutions Acidophilus Blend dietary supplements because they contain undeclared milk, a major food allergen.

    Product
    Dietary Supplement Acidophilus Blend, 90 capsules, Product No. E-420, packaged in 225cc HDPE white bottle, room temp, sold individually
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0011-2017·2016-10-19

    Weis Markets Recalls Bakery Products Due to Metal Fragments

    Weis Markets is voluntarily recalling 30 bakery products, including muffins and cookies, due to potential small metal fragments in the sugar topping.

    Product
    Gourmet Cherry Almond Monster Muffins (4 count)
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-0019-2017·2016-10-19

    Weis Markets Recalls Bakery Products Due to Metal Fragments

    Weis Markets is voluntarily recalling 30 bakery products, including muffins and cookies, due to the potential presence of small metal fragments in the sugar topping.

    Product
    Gourmet Cranberry Orange Monster Muffins (4 count)
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-0012-2017·2016-10-19

    Weis Markets Recalls 30 Bakery Products Due to Metal Fragments

    Weis Markets is voluntarily recalling 30 bakery products, including muffins and cookies, due to potential small metal fragments in the sugar topping.

    Product
    Gourmet Butter Rum Monster Muffins (4 count)
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-0071-2017·2016-10-19

    R.W. Garcia Recalls Central Market Tortilla Chips Due to Metal Fragments

    R.W. Garcia Co., Inc. is recalling Central Market Tortilla Chips, Veggie & Seed Blend, because metal fragments were detected in the raw material.

    Product
    Central Market, Tortilla Chips, Veggie & Seed Blend, Net Wt.; 12oz (340g), Distributed by H.E.B Central Markets, Austin, TX 78735.
    Category
    Food
    Distribution
    0 states
  • HighFDA (Drugs)·D-0038-2017·2016-10-19

    Pharmedium Recalls Fentanyl Citrate Injection Due to Stability Data Concerns

    Pharmedium Services, LLC is recalling 997 syringes of fentanyl citrate injection because stability data does not support the expiry date, posing a potential loss of potency.

    Product
    fentaNYL Citrate Injection, 50 mcg per mL, 250 mcg per 5 mL, 5mL Total Volume in a syringe, For IV Use, Rx only, PharMEDium, Product code 2R3306.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0076-2017·2016-10-19

    R.W. Garcia Kale Crackers Recalled for Metal Fragments

    R.W. Garcia is recalling 49 cases of 3 Seed Kale Crackers due to the detection of metal fragments in raw material.

    Product
    RW Garcia, 3 Seed, Kale Crackers, Gluten Free, Net Wt. 180g, Product of USA, Manufactured & Distributed by R.W. Garcia Co., Inc., Las Vegas, NV 89115 and Lincoln, NC 28092, Distributed by Clean Foods, Ltd, Legion House, 75 Lower Road, Kenley, Surrey, CR8 5NH.
    Category
    Food
    Distribution
    0 states
  • ModerateFDA (Drugs)·D-0048-2017·2016-10-19

    Pharmedium Heparin Syringes Recalled Due to Potential Loss of Potency

    Pharmedium Services, LLC is recalling 240 Heparin Sodium syringes because stability data does not support the expiry date, posing a risk of reduced drug potency.

    Product
    HEPARIN Sodium Inj., USP, 5,000 USP Heparin Units per 5 mL Total Volume in a syringe, NOT FOR LOCK FLUSH, 1,000 USP Heparin Units per mL, Rx only, PharMEDium, Product code 2K1925.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0058-2017·2016-10-19

    Teleflex Gripper Graspers Recalled for Labeling Error

    Teleflex Medical is recalling 160 Gripper Graspers due to a labeling error where they were mislabeled as Johans Graspers.

    Product
    Teleflex Percuaneous Solutions, Gripper Grasper, Ref ML003EE, Rx Only Sterile Manufactured for: Teleflex Medical, Park, NC 27709 The Percutaneous Surgical System with 5 mm attachments is indicated for the means to penetrate soft tissue to access certain areas of the human abdo
    Category
    Medical Device
    Distribution
    6 states
  • ModerateFDA (Drugs)·D-0044-2017·2016-10-19

    Pharmedium Recalls Glycopyrrolate Syringes Due to Stability Data Concerns

    Pharmedium Services, LLC is recalling 16,366 syringes of glycopyrrolate because stability data does not support the expiration dates, posing a risk of reduced drug potency.

    Product
    glycopyrrolate, 0.2 mg per mL, 0.6 mg per 3 mL, 3 mL Total Volume in a syringe, For IV Use, Rx only, PharMEDium, Product code 2R3217.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0061-2017·2016-10-19

    Pharmedium Recalls Lidocaine HCl Syringes Due to Stability Data Concerns

    Pharmedium Services, LLC is recalling 500 syringes of lidocaine HCl 1% because stability data does not support the expiry date, posing a risk of loss of potency.

    Product
    lidocaine HCl, 1%, 30 mg per 3 mL, 3 mL Total Volume in a syringe, Rx only, PharMEDium, Product code 2R3104.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0063-2017·2016-10-19

    A&D Blood Pressure Monitors Recalled for Small Cuff Labeling Error

    A&D Engineering is recalling 378 blood pressure monitors that were not labeled for use with small cuffs. The devices were distributed to distributors in New York, Massachusetts, Virginia, and Texas.

    Product
    Blood Pressure Monitor UA-767PBT-Ci for small cuff. Designed to be used by end users who are eighteen (18) years and older at home to monitor their blood pressure (systolic and diastolic) and pulse rate.
    Category
    Medical Device
    Distribution
    3 states
  • ModerateFDA (Drugs)·D-0031-2017·2016-10-19

    Pharmedium Recalls ePHEDrine Sulfate Syringes Due to Stability Data Concerns

    Pharmedium Services, LLC is recalling 1,545 syringes of ePHEDrine Sulfate because stability data does not support the expiration dates, posing a risk of reduced potency.

    Product
    ePHEDrine Sulfate, 10 mg per mL, in 0.9% Sodium Chloride, Preservative Free, 1 mL Total Volume in a syringe, For IV Use, Rx only, PharMEDium, Product code 2R3347.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0029-2017·2016-10-19

    Pharmedium Recalls Ephedrine Sulfate Syringes Due to Stability Data Concerns

    Pharmedium Services, LLC is recalling 995 syringes of ePHEDrine Sulfate because stability data does not support the expiration dates, posing a risk of loss of potency.

    Product
    ePHEDrine Sulfate, 5 mg per mL, 25 mg per 5 mL, in 0.9% Sodium Chloride, Preservative Free, 5 mL Total Volume in a syringe, For IV Use, Rx only, PharMEDium, Product code 2R3301.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0086-2017·2016-10-19

    Pharmedium Recalls Phenylephrine Syringes Due to Stability Data Concerns

    Pharmedium Services, LLC is recalling 498 syringes of Phenylephrine HCl because stability data does not support the expiry date, posing a risk of loss of potency.

    Product
    PHENYLephrine HCl, 100 mcg per mL, 0.5 mg per 5 mL, in 0.9% Sodium Chloride, Preservative Free, 5 mL Total Volume in a syringe, For IV Use, Rx only, PharMEDium, Product code 2R3109.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0026-2017·2016-10-19

    Pharmedium Recalls Atropine Sulfate Injection Due to Stability Data Concerns

    Pharmedium Services, LLC is recalling 5,568 syringes of atropine sulfate injection because stability data does not support the expiration dates, posing a risk of reduced potency.

    Product
    atropine Sulfate Injection, 0.4 mg per mL, 0.8 mg per 2 mL, 2 mL Total Volume in a syringe, For IV Use, Rx only, PharMEDium, Product code 2R3335.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0053-2017·2016-10-19

    Pharmedium Recalls Ketamine Syringes Due to Potential Loss of Potency

    Pharmedium Services, LLC is recalling 25 syringes of ketamine HCl because stability data does not support the expiry date, posing a risk of reduced drug potency.

    Product
    ketamine HCl, 10 mg per mL, 50 mg per 5 mL, in 0.9% Sodium Chloride, 5 mL Total Volume in a syringe, For IV Use, Rx only, PharMEDium, Product code 2R3234.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0037-2017·2016-10-19

    Pharmedium Recalls Fentanyl Citrate Injection Syringes Due to Stability Concerns

    Pharmedium Services, LLC is recalling 53,357 syringes of fentanyl citrate injection because stability data does not support the expiry dates, posing a risk of loss of potency.

    Product
    fentaNYL Citrate Injection, 50 mcg per mL (100 mcg per 2 mL), 2 mL Total Volume in a syringe, For IV Use, Rx only, PharMEDium, Product code 2R3303.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0088-2017·2016-10-19

    Pharmedium Recalls Remifentanil Syringes Due to Potential Loss of Potency

    Pharmedium Services, LLC is recalling 1,623 syringes of remifentanil HCl because stability data does not support the expiration dates, posing a risk of reduced drug potency.

    Product
    remifentanil HCl, 50 mcg per mL, 100 mcg per 2 mL, in 0.9% Sodium Chloride, Preservative Free, 2 mL Total Volume in a syringe, Rx only, PharMEDium, Product code 2R3300.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0064-2017·2016-10-19

    Winco TMM3 Video-Fluoroscopy Stretcher-Chair Recalled for Non-Conforming Component

    Winco Mfg., LLC is recalling 264 TMM3 Series Video-Fluoroscopy Stretcher-Chairs because a non-conforming component caused the arms to no longer meet design specifications.

    Product
    TransMotion Medical, TMM3 Series Video-Fluoroscopy Swallow Study Stretcher-Chair. Intended use is to provide the caregiver a single platform for receiving, transporting within a facility, performing procedures, recovery and discharge of patients in a monitored outpatient envir
    Category
    Medical Device
    Distribution
    29 states
  • ModerateFDA (Drugs)·D-0083-2017·2016-10-19

    Pharmedium Recalls Neostigmine Methylsulfate Syringes Due to Stability Concerns

    Pharmedium Services, LLC is recalling specific lots of neostigmine methylsulfate syringes because stability data does not support the expiration dates, posing a risk of reduced potency.

    Product
    neostigmine Methylsulfate, 1 mg per mL, 2 mg per 2 mL, 2 mL Total Volume in a syringe, For IV Use, Rx only, PharMEDium, Product code 2R3550.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0082-2017·2016-10-19

    Pharmedium Recalls Neostigmine Methylsulfate Syringes Due to Stability Data Concerns

    Pharmedium Services, LLC is recalling 2,105 syringes of neostigmine methylsulfate because stability data does not support the expiration dates, posing a risk of reduced potency.

    Product
    neostigmine Methylsulfate, 1 mg per mL, 5 mg per 5 mL, 5 mL Total Volume in a syringe, For IV Use, Rx only, PharMEDium, Product code 2R3326.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0059-2017·2016-10-19

    Teleflex Johans Grasper Recall Due to Labeling Error

    Teleflex Medical is recalling 160 Johans Graspers because they were mislabeled as Gripper Graspers. The sterile surgical instruments were distributed to six US states.

    Product
    Teleflex Percuaneous Solutions, Johans Grasper, Ref ML004EE, Rx Only Sterile Manufactured for: Teleflex Medical, Park, NC 27709 The Percutaneous Surgical System with 5 mm attachments is indicated for the means to penetrate soft tissue to access certain areas of the human abdom
    Category
    Medical Device
    Distribution
    6 states
  • ModerateFDA (Drugs)·D-0035-2017·2016-10-19

    Pharmedium Recalls Fentanyl Syringes Due to Potential Loss of Potency

    Pharmedium Services is recalling 8,955 syringes of fentanyl citrate because stability data does not support the expiration dates, posing a risk of reduced drug potency.

    Product
    fentaNYL Citrate, 10 mcg per 1 mL, in 0.9% Sodium Chloride, Preservative Free, 1 mL Total Volume in a syringe, For IV Use, Rx only, PharMEDium, Product code 2R3174.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0044-2017·2016-10-19

    Doctor Kracker Crispbreads Recalled for Incorrect Milk Labeling

    Kracker Enterprises is recalling Doctor Kracker Klassic 3 Seed Crispbreads because the packaging lists milk as an ingredient, even though the product does not contain milk.

    Product
    Doctor Kracker Klassic 3 Seed Crispbreads Net Wt 7 oz (200g) in cardboard container.
    Category
    Food
    Distribution
    10 states
  • ModerateFDA (Drugs)·D-0076-2017·2016-10-19

    Pharmedium Recalls Morphine Sulfate Syringes Due to Stability Data Concerns

    Pharmedium Services, LLC is recalling 3,270 syringes of morphine sulfate due to stability data that does not support the expiry date, posing a potential loss of potency.

    Product
    morphine Sulfate, 0.5 mg per mL, in 0.9% Sodium Chloride, Preservative Free (Contains Sulfites), 1 mL Total Volume in a syringe, For IV use, Rx only, PharMEDium, Product code 2R3017.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0039-2017·2016-10-19

    Schafer Fisheries Recalls Fish Hot Dogs Due to HACCP Record Deficiencies

    Schafer Fisheries is recalling specific lots of fish hot dogs because of inadequate HACCP records. The products were distributed in Illinois, New York, and California.

    Product
    *** 1) Fish hot dogs total 1 lb in weight vacuum packaged in plastic bags; Label reads in part: TWIN FIN DELI; Franks; Net WT. 1lb (453g); Kosher Fish Products Inc. Fulton, IL FDA# 1481764; *** 2) Fish hot dogs total 15 lbs in weight packaged 120 x box with a poly liner
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Drugs)·D-0066-2017·2016-10-19

    Pharmedium Recalls Lidocaine HCl Syringes Due to Stability Data Concerns

    Pharmedium Services, LLC is recalling 830 syringes of lidocaine HCl, 2%, preservative-free, because stability data does not support the expiry dates, posing a risk of potential loss of potency.

    Product
    lidocaine HCl, 2%, Preservative Free, Total Volume 2mL, Product code 2R3323, NDC 61553-323-79
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0071-2017·2016-10-19

    Pharmedium Recalls Methadone Syringes Due to Potential Loss of Potency

    Pharmedium Services, LLC is recalling 200 syringes of methadone HCl because stability data does not support the expiration dates, posing a risk of reduced drug potency.

    Product
    methadone HCl, 2.5 mg per 0.5 mL, in 0.9% Sodium Chloride, 0.5 mL Total Volume in a syringe, For IV Use Only, Rx only, PharMEDium, Product code 2T6134.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0063-2017·2016-10-19

    Pharmedium Recalls Lidocaine HCl Syringes Due to Stability Data Concerns

    Pharmedium Services, LLC is recalling 5,900 syringes of lidocaine HCl 1% because stability data does not support the expiry dates, posing a risk of loss of potency.

    Product
    lidocaine HCl, 1%, in 0.9% Sodium Chloride, Preservative Free, Total Volume 1 mL in a syringe, Rx only, PharMEDium, Product code 2R3345.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0062-2017·2016-10-19

    Pharmedium Recalls Lidocaine HCl Syringes Due to Stability Data Concerns

    Pharmedium Services, LLC is recalling 499 syringes of lidocaine HCl 1% because stability data does not support the expiry date, posing a potential loss of potency.

    Product
    lidocaine HCl, 1%, 10 mg per mL (50 mg per 5 mL), 5 mL Total Volume in a syringe, Rx only, PharMEDium, Product code 2R3106.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0092-2017·2016-10-19

    PharMEDium Recalls Lidocaine Syringes Due to Stability Data Concerns

    PharMEDium is recalling 499 syringes of lidocaine HCl 2% because stability data does not support the expiry date, posing a potential loss of potency.

    Product
    lidocaine HCl, 2%, 20 mg per mL (100 mg per 5 mL), 5 mL Total Volume in a syringe, Rx only, PharMEDium, Product code 2R3110.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0040-2017·2016-10-19

    Schafer Fisheries Recalls Twin Fin Deli Salami Due to Recordkeeping Issues

    Schafer Fisheries is recalling Twin Fin Deli Salami because the company lacked adequate HACCP records. The product was distributed in Illinois, New York, and California.

    Product
    Label reads in part: TWIN FIN DELI; Salami; Net WT. 1lb (453g); P.O. Box 399 Thomson IL, FDA# 1481764 Thomason
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-0066-2017·2016-10-19

    Winco TMM5 Mobile Surgical Stretcher-Chair Recalled for Design Non-Conformance

    Winco Mfg. is recalling 264 TMM5 Series Mobile Surgical Stretcher-Chairs because non-conforming components caused the arms to no longer meet design specifications.

    Product
    TransMotion Medical, TMM5 Series Mobile Surgical Stretcher -Chair. Intended use is to provide the caregiver a single platform for receiving, transporting within a facility, performing procedures, recovery and discharge of patients in a monitored outpatient environment.
    Category
    Medical Device
    Distribution
    29 states
  • ModerateFDA (Food)·F-0045-2017·2016-10-19

    Wegmans Organic Blush Sauce Recalled for Incorrect Milk Allergen Labeling

    LiDestri Foods is recalling Wegmans Organic Blush Sauce because jars were labeled with a cream sauce allergen declaration for milk.

    Product
    Wegmans ITALIAN CLASSICS Organic BLUSH SAUCE, NET WT 23.5 OZ (1 LB 7.5 OZ) 667g
    Category
    Food
    Distribution
    0 states
  • ModerateFDA (Drugs)·D-0051-2017·2016-10-19

    Pharmedium Recalls Hydromorphone Syringes Due to Stability Data Concerns

    Pharmedium Services, LLC is recalling 4,860 syringes of Hydromorphone HCl because stability data does not support the expiration dates, posing a risk of reduced drug potency.

    Product
    HYDROmorphone HCl, 0.5 mg per mL in 0.9% Sodium Chloride, 1 mL Total Volume in a syringe, For IV Use, Rx only, PharMEDium, Product code 2R3352.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0065-2017·2016-10-19

    PharMEDium Lidocaine Syringes Recalled for Potential Loss of Potency

    PharMEDium is recalling lidocaine HCl syringes because stability data does not support the expiration dates, posing a risk of reduced drug potency.

    Product
    lidocaine HCl, 2%, 40 mg per 2 mL, 2 mL Total Volume in a syringe, Rx only, PharMEDium, Product code 2R3112.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0082-2017·2016-10-19

    Chaos and Pain Recalls Cannibal Riot Pre-Workout for Undeclared Ingredients

    Chaos and Pain is recalling Cannibal Riot pre-workout supplements because they contain undeclared Agmatine and 1,3 Dimethylbutylamine, which is not permitted in the EU.

    Product
    CANNIBAL RIOT, SUPER STIMULANT PRE-WORKOUT ENERGY COMPLEX, UNICORN BLOOD, Chaos and Pain, DIETARY SUPPLEMENTS, NET.WT. 10.5 oz (300g), UPC 610563314669
    Category
    Food
    Distribution
    0 states
  • ModerateFDA (Drugs)·D-0060-2017·2016-10-19

    Pharmedium Recalls Lidocaine HCl Syringes Due to Stability Data Concerns

    Pharmedium Services, LLC is recalling 2,961 syringes of lidocaine HCl 1% because stability data does not support the expiration dates, posing a risk of reduced potency.

    Product
    lidocaine HCl, 1%, 10 mg per 1 mL, 1 mL Total Volume in a syringe, Rx only, PharMEDium, Product code 2R3102.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0032-2017·2016-10-19

    Pharmedium Recalls Fentanyl and Bupivacaine Syringes Due to Stability Data Concerns

    Pharmedium Services, LLC is recalling 210 syringes of Fentanyl Citrate and Bupivacaine HCl because stability data does not support the expiration dates, posing a risk of loss of potency.

    Product
    Fentanyl Citrate 16.67 mcg per mL and Bupivacaine HCl 0.1667% in 0.9% Sodium Chloride, Total Dose 25.005 mcg/1.5 mL Fentanyl Citrate, Content Volume 1.5 mL in 3 mL BD Syringe, Intended for Epidural Use, Rx only, PharMEDium, Product code 2T6228.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0058-2017·2016-10-19

    Pharmedium Recalls Labetalol HCl Syringes Due to Stability Data Concerns

    Pharmedium Services, LLC is recalling 969 syringes of labetalol HCl because stability data does not support the expiry dates, posing a risk of loss of potency.

    Product
    labetalol HCl, 5 mg per mL, 20 mg per 4 mL, 4 mL total Volume in a syringe, For IV Use, Rx only, PharMEDium, Product code 2R3117.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0059-2017·2016-10-19

    Pharmedium Recalls Lidocaine Syringes Due to Potential Loss of Potency

    Pharmedium Services, LLC is recalling 3,285 syringes of lidocaine HCl because stability data does not support the expiry date, posing a risk of reduced drug potency.

    Product
    lidocaine HCl, 0.5%, 5 mg per mL, in 0.9% Sodium Chloride, 1 mL Total Volume in a syringe, Rx only, PharMEDium, Product code 2R3140.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0072-2017·2016-10-19

    Pharmedium Recalls Methadone Syringes Due to Potential Loss of Potency

    Pharmedium Services, LLC is recalling 7,556 syringes of methadone HCl because stability data does not support the expiration dates, posing a risk of reduced drug potency.

    Product
    methadone HCl, 10 mg per mL, 1 mL Total Volume in a syringe, For IV Use Only, Rx only, PharMEDium, Product code 2T6149.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0043-2017·2016-10-19

    Pharmedium Recalls Fentanyl Citrate Syringes Due to Stability Data Concerns

    Pharmedium Services, LLC is recalling specific lots of fentanyl citrate syringes because stability data does not support the expiration dates, posing a risk of reduced potency.

    Product
    fentaNYL Citrate, 5 mcg per mL (10 mcg per 2 mL) in 0.9% Sodium chloride, 2 mL Total Volume in a 3 mL BD Syringe, For IV Use Only, Rx only, PharMEDium, Product code 2T6107.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0099-2017·2016-10-19

    Allergan Recalls Tazorac Gel 0.05% Due to Content Uniformity Failures

    Allergan Sales, LLC is recalling Tazorac (tazarotene) Gel 0.05% because it failed content uniformity specifications. The recall covers 25,247 tubes distributed nationwide.

    Product
    TAZORAC (tazarotene) Gel 0.05%, Rx only, For Dermatologic Use Only, Not for Ophthalmic Use, packaged in a) 30 g tubes (NDC: 0023-8335-03, UPC: 300238335036) and b)100 g tubes,(NDC: 0023-8335-10, UPC: 300238335104), Manufactured by: Allergan Inc., Irvine, CA 92512.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0030-2017·2016-10-19

    Pharmedium Recalls ePHEDrine Sulfate Syringes Due to Stability Data Concerns

    Pharmedium Services, LLC is recalling 1,478 syringes of ePHEDrine Sulfate because stability data does not support the expiration dates, posing a risk of reduced potency.

    Product
    ePHEDrine Sulfate, 10 mg per mL, 50 mg per 5 mL, in 0.9% Sodium Chloride, Preservative Free, 5 mL Total Volume in a syringe, For IV Use, Rx only, PharMEDium, Product code 2R3308.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0045-2017·2016-10-19

    Pharmedium Recalls Glycopyrrolate Syringes Due to Stability Data Concerns

    Pharmedium Services, LLC is recalling 17,462 syringes of glycopyrrolate because stability data does not support the expiration dates, posing a risk of reduced potency.

    Product
    glycopyrrolate, 0.2 mg per mL, 0.4 mg per 2 mL, 2 mL Total Volume in a syringe, For IV Use, Rx only, PharMEDium, Product code 2R3329.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0068-2017·2016-10-19

    Pharmedium Recalls Lidocaine HCl Syringes Due to Stability Data Concerns

    Pharmedium Services, LLC is recalling 1,161 syringes of lidocaine HCl 2% because stability data does not support the expiration dates, posing a risk of reduced potency.

    Product
    lidocaine HCl, 2%, 20 mg per mL (60 mg per 3 mL), 3 mL Total Volume, Product code 2R3441, NDC 61553-441-80
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0089-2017·2016-10-19

    Pharmedium Recalls Rocuronium Bromide Syringes Due to Stability Data Concerns

    Pharmedium Services, LLC is recalling 6,970 syringes of rocuronium bromide because stability data does not support the expiration dates, posing a risk of reduced drug potency.

    Product
    rocuronium Bromide, 10 mg per mL, 50 mg per 5 mL, Preservative Free, 5 mL Total Volume in a syringe, For IV Use, Rx only, PharMEDium, Product code 2R3321.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0047-2017·2016-10-19

    Pharmedium Recalls Heparin Sodium Injections Due to Stability Data Concerns

    Pharmedium Services, LLC is recalling 399 syringes of Heparin Sodium Injection because stability data does not support the expiration dates, posing a risk of loss of potency.

    Product
    HEPARIN Sodium Inj. USP, 15,000 USP Heparin Units per 3 mL Injection 3 mL Total Volume in a syringe, Rx only, PharMEDium, Product code 2K1210.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0084-2017·2016-10-19

    Pharmedium Recalls Neostigmine Methylsulfate Syringes Due to Stability Data Concerns

    Pharmedium Services, LLC is recalling 700 syringes of neostigmine methylsulfate because stability data does not support the expiration dates, posing a risk of reduced potency.

    Product
    neostigmine Methylsulfate, 1 mg per mL, 3 mg per 3 mL, 3 mL Total Volume in a syringe, For IV Use, Rx only, PharMEDium, Product code 2R3551.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0084-2017·2016-10-19

    Morrison Milling Recalls Whole Wheat Flour for Potential Nylon Fragments

    Morrison Milling is recalling 5 lb bags of The Baker's Scoop 100% Whole Wheat Flour due to the potential presence of soft nylon fragments.

    Product
    The Baker's Scoop 100% WHOLE WHEAT FLOUR NET WT. 5 LB (2.27 kg) packaged in white paper bag
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·F-0069-2017·2016-10-19

    Supermom's Kitchen Roast Beef Melt Recalled for Undeclared Ingredients

    Northern Tier Bakery is recalling Supermom's Kitchen Roast Beef & Cheddar Melt because the product was mislabeled and failed to declare monosodium glutamate, yellow 5, and yellow 6.

    Product
    Supermoms Kitchen Roast Beef & Cheddar Melt, Net Wt. 3.7 oz (105g). Keep Refrigerated. UPC 63913-94236
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Food)·F-0041-2017·2016-10-19

    Schafer Fisheries Recalls Gefilte Fish Due to HACCP Record Deficiencies

    Schafer Fisheries is recalling 250 cases of Twin Fin Deli Gefilte Fish because the company lacked adequate HACCP records. The product was distributed in Illinois, New York, and California.

    Product
    Label reads in part: TWIN FIN DELI; Gefilte Fish; Kosher Fish Products Inc., Fulton, IL. FDA# 1481764; Net WT. 24 OZ (680G)
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Food)·F-0081-2017·2016-10-19

    Chaos and Pain Recalls Cannibal Riot Pre-Workout for Undeclared Ingredients

    Chaos and Pain is recalling Cannibal Riot pre-workout supplements because they contain undeclared Agmatine and 1,3 Dimethylbutylamine, which is not permitted in the EU.

    Product
    CANNIBAL RIOT, SUPER STIMULANT PRE-WORKOUT ENERGY COMPLEX, FIVE FINGER DEATH PUNCH, Chaos and Pain, DIETARY SUPPLEMENTS, NET.WT. 10.5 oz (300g), UPC 610563314652
    Category
    Food
    Distribution
    0 states
  • ModerateFDA (Drugs)·D-0027-2017·2016-10-19

    Pharmedium Recalls Buffered Lidocaine Syringes Due to Stability Data Concerns

    Pharmedium Services, LLC is recalling 660 syringes of Buffered Lidocaine because stability data does not support the expiry dates, posing a risk of potency loss.

    Product
    Buffered Lidocaine, 1%, In Sodium Bicarbonate 8.4%, 1 mL Total Volume in a syringe, Local anesthetic use, Rx only, PharMEDium, Product code 2K2466.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0079-2017·2016-10-19

    Pharmedium Recalls Morphine Sulfate Syringes Due to Stability Data Concerns

    Pharmedium Services, LLC is recalling 21,506 syringes of morphine sulfate because stability data does not support the expiry dates, posing a risk of potency loss.

    Product
    morphine Sulfate, 1 mg per mL (2 mg per 2 mL), in 0.9% Sodium Chloride, Preservative Free (Contains Sulfites), 2 mL Total Volume in a syringe, For IV use, Rx only, PharMEDium, Product code 2R3259.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0033-2017·2016-10-19

    Fentanyl Citrate Injection Recalled Due to Potential Loss of Potency

    Pharmedium Services is recalling fentanyl citrate injection syringes because stability data does not support the expiration date, posing a risk of reduced drug potency.

    Product
    fentaNYL Citrate Injection, 50 mcg per mL, Preservative Free, 1 mL Total Volume in a syringe, For IV Use, Product code 2R3118, NDC 61553-118-40
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0041-2017·2016-10-19

    Pharmedium Recalls Fentanyl Citrate Syringes Due to Stability Data Concerns

    Pharmedium Services, LLC is recalling 616 syringes of fentanyl citrate because stability data does not support the expiry dates, posing a risk of loss of potency.

    Product
    fentaNYL Citrate, 10 mcg per mL (25 mcg per 2.5 mL), in 0.9% Sodium Chloride, 2.5 mL Total Volume in a syringe, For IV Use, Rx only, PharMEDium, Product code 2R3424.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0067-2017·2016-10-19

    Pharmedium Recalls Lidocaine HCl Syringes Due to Stability Data Concerns

    Pharmedium Services, LLC is recalling 512 syringes of lidocaine HCl 2% because stability data does not support the expiry date, posing a potential loss of potency.

    Product
    lidocaine HCl 2%, Preservative Free, 20 mg per mL (100 mg per 5 mL), 5 mL Total Volume in a syringe, Rx only, PharMEDium, Product code 2R3384.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0074-2017·2016-10-19

    Pharmedium Recalls Midazolam HCl Syringes Due to Stability Data Concerns

    Pharmedium Services, LLC is recalling 4,058 syringes of midazolam HCl because stability data does not support the expiration dates, posing a risk of reduced potency.

    Product
    midazolam HCl, 1 mg per mL (3 mg per 3 mL), in 0.9% Sodium Chloride, 3 mL Total Volume in a syringe, For IV Use, Rx only, PharMEDium, Product Code 2R3351.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0064-2017·2016-10-19

    Pharmedium Recalls Lidocaine HCl Syringes Due to Stability Data Concerns

    Pharmedium Services, LLC is recalling 300 syringes of lidocaine HCl 1% because stability data does not support the expiry date, posing a potential loss of potency.

    Product
    lidocaine HCl 1%, 10 mg per mL (50 mg per 5 mL), Preservative Free, 5 mL Total Volume in a syringe, Rx only, PharMEDium, Product code 2R3391.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0028-2017·2016-10-19

    Pharmedium Recalls Buffered Lidocaine Syringes Due to Stability Data Concerns

    Pharmedium Services, LLC is recalling 10 syringes of Buffered Lidocaine 2% because stability data does not support the expiry date, posing a risk of loss of potency.

    Product
    Buffered Lidocaine, 2%, In Sodium Bicarbonate 8.4%, 3 mL Total Volume in a syringe, Local anesthetic use, Rx only, PharMEDium, Product code 2K2475.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0046-2017·2016-10-19

    Pharmedium Recalls Glycopyrrolate Syringes Due to Insufficient Stability Data

    Pharmedium Services, LLC is recalling specific lots of glycopyrrolate syringes because stability data does not support the expiration dates, posing a risk of reduced potency.

    Product
    glycopyrrolate, 0.2 mg per mL, 1 mg per 5 mL, 5 mL Total Volume in a syringe, For IV Use, Rx only, PharMEDium, Product code 2R3340.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0050-2017·2016-10-19

    Pharmedium Recalls Hydromorphone Syringes Due to Stability Data Concerns

    Pharmedium Services, LLC is recalling 1,916 syringes of Hydromorphone HCl because stability data does not support the expiration dates, posing a risk of reduced potency.

    Product
    HYDROmorphone HCl, 0.2 mg per mL, (0.4 mg per 2 mL), in 0.9% Sodium Chloride, 2 mL Total Volume in a syringe, For IV Use, Rx only, PharMEDium, Product code 2R3162.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0054-2017·2016-10-19

    Pharmedium Recalls Ketamine HCl Syringes Due to Stability Data Concerns

    Pharmedium Services, LLC is recalling 1,500 syringes of ketamine HCl because stability data does not support the expiration dates, posing a risk of reduced drug potency.

    Product
    ketamine HCl, 10 mg per mL, 50 mg per 5 mL, 0.9% Sodium Chloride, 5 mL Total Volume in a syringe, For IV Use, Rx only, PharMEDium, Product code 2R3320.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0055-2017·2016-10-19

    Pharmedium Recalls Ketamine HCl Syringes Due to Stability Data Concerns

    Pharmedium Services, LLC is recalling 9,101 syringes of ketamine HCl because stability data does not support the expiration dates, posing a risk of reduced potency.

    Product
    ketamine HCl, 10 mg per mL, 20 mg per 2 mL, in 0.9% Sodium Chloride, 2 mL Total Volume in a syringe, For IV Use, Rx only, PharMEDium, Product code 2R3330.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0065-2017·2016-10-19

    Winco TMM4 Series Treatment Chair Recalled for Non-Conforming Component

    Winco Mfg. is recalling 264 TMM4 Series Multi-Purpose Treatment Chairs because a non-conforming component caused the arms to no longer meet design specifications.

    Product
    TransMotion Medical, TMM4 Series Multi-Purpose Treatment Chair. Intended use is to provide the caregiver a single platform for receiving, transporting within a facility, performing procedures, recovery and discharge of patients in a monitored outpatient environment.
    Category
    Medical Device
    Distribution
    29 states
  • ModerateFDA (Devices)·Z-0084-2017·2016-10-19

    Zimmer Biomet Recalls Phoenix Recon Targeting Arm Surgical Instruments

    Zimmer Biomet is recalling 31 Phoenix Recon Targeting Arm surgical instruments because old and new revisions are not interchangeable, potentially causing surgical delays.

    Product
    Phoenix Recon Targeting Arm Guide, Surgical, Instrument for the sleeve and Orthopedic Manual Surgical Instruments for the Arm Product Usage: The Phoenix Femoral Nail System is to be implanted into the femur for alignment, stabilization and fixation of fractures caused by tra
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0079-2017·2016-10-19

    RaySearch Radiation Therapy Treatment Planning System Software Recall

    RaySearch Laboratories is recalling Model 5.0 software due to a bug that may display incorrect dose statistics in treatment plan reports.

    Product
    Radiation Therapy Treatment Planning System, Model 5.0
    Category
    Medical Device
    Distribution
    9 states
  • ModerateFDA (Devices)·Z-0083-2017·2016-10-19

    Zimmer Biomet Recalls Phoenix Recon Soft Tissue Sleeve Guide Instruments

    Zimmer Biomet is recalling 31 Phoenix Recon Soft Tissue Sleeve Guides due to incompatibility with new revision targeting arms, which may cause surgical delays.

    Product
    Phoenix Recon Soft Tissue Sleeve Guide, Surgical, Instrument for the sleeve and Orthopedic Manual Surgical Instruments for the Arm Product Usage: The Phoenix Femoral Nail System is to be implanted into the femur for alignment, stabilization and fixation of fractures caused b
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0068-2017·2016-10-19

    Surgical Specialties Recalls BioSentry Tract Sealant System Due to Packaging Defect

    Surgical Specialties Mexico is recalling the BioSentry Tract Sealant System because the product packages may have open seals.

    Product
    BioSentry Tract Sealant System, Product Code: 768022019S; Indicated to provide accuracy in marking a biopsy location for visualization during surgical resection.
    Category
    Medical Device
    Distribution
    20 states
  • LowFDA (Drugs)·D-0095-2017·2016-10-19

    Teva Recalls MitoXANTRONE Injection Due to Potential Impurity D Failure

    Teva Pharmaceuticals USA is recalling MitoXANTRONE Injection USP vials nationwide because they may fail to meet specifications for Impurity D throughout their shelf life.

    Product
    mitoXANTRONE Injection USP (concentrate), 20 mg/10 mL (2 mg/mL), 10 mL Multiple Dose Vial, Rx only, Teva Parenteral Medicines, Inc., Irvine, CA 92618, NDC 0703-4685-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0098-2017·2016-10-19

    Dr. Reddy's Recalls ZENATANE Isotretinoin Capsules for Dissolution Failures

    Dr. Reddy's Laboratories is recalling ZENATANE (isotretinoin) 20 mg capsules because they failed to meet dissolution specifications. The recall covers 3,858 prescription packs distributed nationwide.

    Product
    ZENATANE — ZENATANE (ISOTRETINOIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0057-2017·2016-10-19

    Circulatory Technology Recalls Better-Bladder Devices Due to Cosmetic Defects

    Circulatory Technology Inc is recalling 958 units of Better-Bladder devices with 14-inch tubing due to twisted or wrinkled balloon components.

    Product
    The Better-Bladder With 14" ID tubing, ITEM BB14, STERILE, Measure pressure noninvasively in the extracorporeal circuit and provide compliance in the venous line between the patient and the pump.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0009-2017·2016-10-19

    Amerisource Health Services Recalls Paricalcitol Capsules Due to Impurities

    Amerisource Health Services is recalling 648 cartons of Paricalcitol Capsules, 1 mcg, due to failed impurities specifications.

    Product
    Paricalcitol Capsules, 1 mcg, packaged in 30 Capsules (5 x 6) per carton (NDC 60687-106-25); each blister card containing 6 individually blistered capsules (NDC 60687-106-95), Rx only, Distributed by: American Health Packaging, Columbus, OH, 43217.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereCPSC·17017·2016-10-18

    3 Squares Rice and Slow Cookers Recalled for Fire and Shock Hazards

    Sherwood Marketing is recalling 3 Squares rice and slow cookers because improperly installed wiring can cause electrical shorting, posing fire and electric shock risks.

    Product
    3 Squares rice and slow cookers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V752000·2016-10-18

    Polaris Recalls 2016-2017 Slingshot Motorcycles for Brake Seal Defect

    Polaris is recalling 2016-2017 Slingshot motorcycles because an over-tightened brake pressure switch may leak fluid, reducing brake performance and increasing crash risk.

    Product
    POLARIS — POLARIS SLINGSHOT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17009·2016-10-18

    Husqvarna Recalls Lawn Mowers Due to Laceration Hazard

    Husqvarna is recalling about 235,000 walk-behind gas-powered lawn mowers because the operator presence control bar can malfunction, causing the engine and blades to continue running and posing a laceration hazard.

    Product
    Lawn mowers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·17016·2016-10-18

    TUSA Recalls Diving Computers Due to Drowning and Injury Hazards

    TUSA is recalling about 175 DC Solar Link IQ1204 diving computers because they may malfunction and display incorrect readings, posing a drowning and injury hazard.

    Product
    Diving computers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16V751000·2016-10-18

    Forest River Surveyor Recalled for Incorrect Federal Tire Placard

    Forest River is recalling 2016-2017 Surveyor recreational vehicles because the Federal Placard lists incorrect tire and rim specifications, which could lead to over-inflation and tire failure.

    Product
    FOREST RIVER — FOREST RIVER SURVEYOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V749000·2016-10-18

    Forest River Recalls 2016-2017 StarTrans and Glaval Transit Buses

    Forest River is recalling 2016-2017 StarTrans and Glaval transit buses because the instrument cluster may display 'PARK' instead of 'BRAKE' during a brake malfunction, increasing crash risk.

    Product
    GLAVAL BUS — GLAVAL BUS, STARTRANS LEGACY, PS2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V746000·2016-10-17

    BMW Recalls 136,188 Vehicles for Fuel Pump Wire Contact Defect

    BMW is recalling 136,188 vehicles from 2007-2012 due to a fuel pump defect that may cause a fuel leak or engine stall.

    Product
    BMW — BMW X5, 535I, 528I, 5-SERIES GRAN TURISMO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V747000·2016-10-17

    BMW Recalls 2016-2017 Models for Driver Seat Belt Retraction Defect

    BMW is recalling approximately 15,455 vehicles because the driver's seat belt may not lock properly during a crash, increasing injury risk.

    Product
    BMW — BMW, MINI, ROLLS-ROYCE X1, COOPER S, COOPER CONVERTIBLE, 528I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V743000·2016-10-17

    Seagrave Heavy Rescue Body Fire Truck Recall for Steering Lock Risk

    Seagrave is recalling one 2010 Heavy Rescue Body Fire Truck because power steering fluid may overheat, causing the steering to lock unexpectedly.

    Product
    SEAGRAVE — SEAGRAVE HEAVY RESCUE BODY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V748000·2016-10-17

    Jayco Recalls 2017 Jay Sport Trailers Due to Tire Rubbing Risk

    Jayco is recalling 2017 Jay Sport camping trailers because tires may rub against wheel wells, potentially causing a blowout and increasing crash risk.

    Product
    JAYCO TRAVEL TRAILER — JAYCO TRAVEL TRAILER JAY SERIES SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide

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