The Recall Desk

Archive

April 2023 recalls

411 recalls were announced in April 2023.

What the numbers show

Critical
6
Severe
53
High
277
Moderate
71
Low
4

Of the 411 recalls this month scored against our rubric, 1% are Critical, 13% are Severe.

Which agencies issued them

401–411 of 411

  • ModerateFDA (Food)·F-0679-2023·2023-04-05

    Cucumber Pickle Recalled for Ingredients Statement Correction

    Lemonland Food Corp is recalling Cucumber Pickle in 8-ounce containers distributed in Washington from February 16–23, 2023, due to an incorrect ingredients statement. The firm provided an updated statement to consignees.

    Product
    Cucumber Pickle distributed in un-labeled plastic containers 8oz. Containers were then labeled at H-mart, G-mart, or M2M retail store.
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0483-2023·2023-04-05

    Drug Recall: Simvastatin 5 mg tablets due to manufacturing compliance violations

    Direct Rx is recalling 51 bottles of Simvastatin 5 mg tablets nationwide due to Good Manufacturing Practice deviations. The recall is voluntary and was initiated in March 2023.

    Product
    Simvastatin, USP, 5 mg Tablets, Rx Only, Packaged as a 90-count bottle, NDC 61919-0710-90 Packaged and Distributed By: Direct Rx, Dawsonville, GA 30534
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0486-2023·2023-04-05

    Simvastatin Tablets Recalled Nationwide Over Manufacturing Practice Deviations

    Direct Rx is recalling 269 bottles of Simvastatin 40 mg nationwide due to Good Manufacturing Practice deviations. No adverse events have been reported. Consult your healthcare provider before changing your medication.

    Product
    Simvastatin, USP, 40 mg, Rx Only, Packaged as a 90-count bottle, NDC 61919-0431-90, Packaged and Distributed By: Direct Rx, Dawsonville, GA 30534
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0482-2023·2023-04-05

    Glimepiride tablet recall due to manufacturing practice deviations

    Direct Rx is recalling Glimepiride 4 mg tablets nationwide due to manufacturing process deviations. The recall is voluntary and affects specific lots of 30-count and 90-count bottles.

    Product
    Glimepiride, USP, 4 mg Tablets, Rx Only, Packaged as a a) 30-count bottle, NDC 61919-0250-30; b) 90-count bottle, NDC 61919-0250-90 Packaged and Distributed By: Direct Rx, Dawsonville, GA 30534
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1317-2023·2023-04-05

    Shoulder Glenoid Prosthesis Implant Manufactured Without Tantalum Markers

    A shoulder glenoid prosthesis implant (SMR TT Hybrid Std - Peg S) was manufactured without tantalum markers that aid in radiographic visualization. While alternative assessment methods using joint space, peg position, and cement observation remain available, the missing markers limit direct imaging capabilities.

    Product
    SMR TT Hybrid glenoid Std - Peg S, REF: 1379.59.210
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-1307-2023·2023-04-05

    ACL ELITE PRO analyzer test definition removal for Anti-Xa reagent

    Instrumentation Laboratory is removing test definitions for HemosIL Liquid Anti-Xa reagent from ACL Elite and Elite Pro analyzers with Serial Number 16053360R and prior. The recall affects 33 units distributed worldwide.

    Product
    ACL ELITE PRO Refurbished)-Analyzer designed specifically for clinical use in the hemostasis laboratory, for coagulation and/or fibrinolysis testing. Part Number: 0001000311R
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·23E030000·2023-04-04

    Cummins Recalls Onan Generator Sets Due to Fuel Hose Fire Risk

    Cummins is recalling certain Onan QG 2800i generator sets because a fuel hose may not be properly secured, creating a gas leak and fire risk.

    Product
    EQUIPMENT:RECREATIONAL VEHICLE/TRAILER recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V237000·2023-04-04

    Freightliner and FCCC trucks recalled for windshield wiper linkage failure

    Daimler Trucks North America is recalling certain 2020-2022 Freightliner and FCCC trucks due to windshield wiper linkage failure that can reduce visibility. Dealers will inspect and replace affected parts free of charge.

    Product
    FREIGHTLINER — FREIGHTLINER, FCCC M2, S2C, S2RV, S2G
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V238000·2023-04-04

    Tie rod fastener defect in commercial trucks risks steering failure

    Daimler Trucks is recalling commercial vehicles with a tie rod that may be missing a fastener, allowing the steer arm to detach and causing potential loss of steering control.

    Product
    FCCC — FCCC, FREIGHTLINER, WESTERN STAR MT50E, 114SD, M2, 4700
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23E029000·2023-04-03

    Cruise Recalls Autonomous Driving Software Due to Crash Risk

    Cruise LLC is recalling certain Automated Driving Systems with specific software versions that may inaccurately predict the movement of articulated vehicles, increasing the risk of a crash.

    Product
    ELECTRICAL SYSTEM:ADAS:AUTONOMOUS/SELF DRIVING:SOFTWARE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide

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