The Recall Desk

State

Louisiana product recalls

73,716 recalls have nationwide distribution and so reach Louisiana. 6,965 additional recalls listed Louisiana specifically in their distribution scope.

What the numbers show

Total
6,965
Critical
1,107
Severe
1,739
Most recent
2026-10-28

Of the 6,965 recalls naming Louisiana we have scored against our rubric, 1,107 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,739 (25%) are Severe.

Which agencies issued them

These figures cover only the 6,965 recalls whose distribution notice names Louisiana specifically. The 73,716 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

30001–30025 of 80681

  • ModerateFDA (Devices)·Z-3029-2020·2020-10-07

    Ameditech Recalls Alere iScreen Single Drug Detection Dip Cards

    Ameditech is recalling Alere iScreen Single Drug Detection dip cards because they may fail to consistently detect certain compounds at labeled levels.

    Product
    Alere iScreen Single Drug Detection (AMT Item Number/ AMT Description): X11-IS1 BUP-DX/ "Alere iScreen" Dx Single Dip Card Single Drug Detection: Buprenorphine (BUP)", X11-IS1 BAR-DX /"Alere iScreen" Dx Single Dip Card Single Drug Detection: Barbiturate (BAR)", X11-IS1…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3051-2020·2020-10-07

    Ameditech Drug Screening Components Recalled for Performance Failures

    Ameditech Inc is recalling specific drug screening components because they failed to consistently detect compounds at labeled levels.

    Product
    Drug Screening Component: Uncut Sheets Part Number/ Description/ LOT Number 100163/ EDI OPI (300) Uncut Sheet-Card /187876, 100195/ EDI PPX Uncut Sheet-Card/ 187877, 160130/ EDI COC Uncut Sheet-Cup/ 188168, 160180/ EDI PCP Uncut Sheet-Cup/ 189027, 160140/ EDI THC Uncut…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3016-2020·2020-10-07

    Cardinal Health Pre-Op Decolonization Kit Recall for Missing Nasal Swabs

    Cardinal Health is recalling pre-operative decolonization kits that contain only one nasal swab instead of the four required for proper treatment.

    Product
    KIT, PRE OP DRAH - Product Usage: Preoperative kit used to decolonize intranasal S. aureus.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3048-2020·2020-10-07

    Ameditech Recalls First Check 2 Panel Drug Cups Due to Performance Failures

    Ameditech is recalling 41,340 units of First Check 2 Panel Drug Cups because the products failed to consistently detect compounds at labeled levels.

    Product
    First Check 2 Panel Drug Cup: (THC/COC); AMT Item Number 990600B
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1627-2020·2020-10-07

    pH-D Boric Acid Vaginal Suppositories Recalled for Lack of FDA Approval

    pH-D Feminine Health is recalling Boric Acid Vaginal Suppositories because they were marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA).

    Product
    pH-D Feminine Health Boric Acid Vaginal Suppositories, 24 vaginal suppositories per box, 600 mg each, pH-D Feminine Health, LLC Madison, TN 37115, UPC Code: 3 49597 00044 5.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3031-2020·2020-10-07

    Ameditech Recalls Alere iCup Drug Detection Cups Due to Performance Failures

    Ameditech Inc is recalling Alere iCup Drug Detection cups because immunoassay enzymes failed performance tests, preventing consistent detection of compounds.

    Product
    Alere iCup Drug Detection (AMT Item Number/ AMT Description): I-DXA-10/ "Alere" iCup¿ Dx 10 Drug Detection + Adulteration AMP/BAR/BZO/COC/MET/MDMA/MTD/MOP/OXY/THC Bl, Cr, Ni, pH, SG", I-DXA-13B/"Alere" iCup¿ DX Drug Screen Cup 13 Drug Detection + Adulteration…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3034-2020·2020-10-07

    Ameditech Fastect II Drug Screen Dipstick Tests Recalled for Performance Failures

    Ameditech is recalling Fastect II Drug Screen Dipstick Tests because they failed to consistently detect compounds at labeled levels.

    Product
    Fastect¿ II Drug Screen Dipstick Test Single Drug Detection (AMT Item Number/ AMT Description): MF25/ "Fastect¿ II Drug Screen Dipstick Test Single Drug Detection: BUP10", QF09/"Fastect¿ II Drug Screen Dipstick Test, 4 Drug Detection: THC50+COC300+OPI300+BZO300", MF20…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3044-2020·2020-10-07

    Ameditech Recalls TDDA Drugs of Abuse Cups Due to Performance Failures

    Ameditech Inc is recalling TDDA Drugs of Abuse Cups because the immunoassay enzymes failed to consistently detect all compounds at labeled levels.

    Product
    TDDA Drugs of Abuse Cup(AMT Item/ AMT Description): TDDA-6MBAU-CUP /"TDDA Drugs of Abuse Cup AMP300/BZO200/COC300/MET300/OPI300/ THC50 with Cr, Ni, pH, Bl, S.G."
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3028-2020·2020-10-07

    Beckman Coulter Recalls UIBC Reagent Lot 2690 Due to Erroneous Results

    Beckman Coulter is recalling 219 units of UIBC reagent lot 2690 because it produces erroneously high patient results at the low end of the linear range.

    Product
    UIBC; Catalog Number: OSR61205; UDI (01) 15099590011925; IVD; Rx Only; WARNING H316 H317 H351 H373 H411 - Product Usage: System reagent for the quantitative determination of Unsaturated Iron Binding Capacity (UIBC) in human serum and plasma on Beckman Coulter AU analyzers.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3040-2020·2020-10-07

    Ameditech iCup Dx14 Drug Screen Cup Recalled for Performance Failures

    Ameditech is recalling iCup Dx14 Drug Screen Cups because immunoassay enzymes failed performance tests, causing inconsistent detection of compounds.

    Product
    iCup Dx14 Drug Screen Cup(AMT Item Number/ AMT Description): X11-I-DXA-2147-011/ "iCup" Dx 14 Drug Screen Cup 14 Drug Detection: (THC50/COC150)+(MOP300/MET500)+(AMP500/BZO300)+ (BAR300/MTD300)+(BUPG10/TCA1000)+(MDMA500/OXY100)+(PCP25/PPX300) 5 Adulteration Tests: Cr, Ni…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3047-2020·2020-10-07

    Ameditech Recalls First Check 14 Panel Drug Cups Due to Performance Failures

    Ameditech is recalling 47,005 units of First Check 14 Panel Drug Cups because immunoassay enzymes failed performance tests, preventing consistent detection of compounds.

    Product
    First Check 14 Panel Drug Cup: (BMC style); AMT Item Number 990700B
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1625-2020·2020-10-07

    Arbor Pharmaceuticals Recalls Subpotent Nymalize Oral Solution

    Arbor Pharmaceuticals is voluntarily recalling Nymalize (nimodipine) oral solution because the drug is subpotent. The FDA classifies this as a Class III recall.

    Product
    Nymalize (nimodipine) oral solution, 60 mg/20 mL, 12 Unit-Dose Cups and 12 Oral Syringes, 2 inner cartons per outer shipping carton, Rx Only, Distributed by arbor Atlanta, GA, NDC 24338-200-12
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V614000·2020-10-06

    Ferrari Recalls 812 Superfast Vehicles for Rear Window Adhesion Defect

    Ferrari is recalling 2018-2020 812 Superfast vehicles because the rear window may have been bonded incorrectly, potentially leading to detachment and increased crash risk.

    Product
    FERRARI — FERRARI 812 SUPERFAST
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V615000·2020-10-06

    Motorhome propane stove gas leak recall affects 2020-2021 models

    REV is recalling certain 2020-2021 Fleetwood and Holiday Rambler motorhomes with Dometic propane stoves due to potential gas leaks that could increase fire risk. Owners should contact REV for free repair at 1-800-509-3417.

    Product
    HOLIDAY RAMBLER — HOLIDAY RAMBLER, FLEETWOOD ADMIRAL, FLAIR, BOUNDER, SOUTHWIND
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20E075000·2020-10-06

    TriMark Recalls 50-200 Door Latches for Emergency Vehicles

    TriMark is recalling 50-200 door latches used in emergency vehicles because trip levers may fail, preventing doors from opening.

    Product
    LATCHES/LOCKS/LINKAGES:DOORS:LATCH recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20E074000·2020-10-06

    Lippert Components Recalls Electric Motors in Power Bedlift Systems

    Lippert Components is recalling electric motors in Power Bedlift systems because internal gear failure may cause the bed to extend unexpectedly, increasing injury risk.

    Product
    EQUIPMENT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V617000·2020-10-06

    Vespa GTS 300 and GTV 300 Scooters Recalled for Brake Pipe Defect

    Piaggio is recalling 2020-2021 Vespa GTS 300 and GTV 300 scooters because improperly galvanized brake pipe terminals can reduce braking efficiency and increase crash risk.

    Product
    VESPA — VESPA GTS 300, GTV 300
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V616000·2020-10-06

    REV Recalls 2019 Road Rescue Type I Ambulances for Door Latch Defect

    REV Ambulance Group is recalling 2019 Road Rescue Type I ambulances because incorrect material in door latches may prevent doors from opening, creating a lock-in risk.

    Product
    ROAD RESCUE — ROAD RESCUE TYPE I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V611000·2020-10-05

    Yamaha Recalls YZF-R3, XMAX, and MT-03 Models for Rear Reflector Defect

    Yamaha is recalling specific 2015-2020 motorcycles and scooters because condensation on the rear reflector lens may reduce its effectiveness, increasing crash risk.

    Product
    YAMAHA — YAMAHA YZF-R3, XMAX, redundant YZF-R3, MT-03
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V613000·2020-10-05

    Volvo Recalls 2020 VNL Trucks for Window Hinge Defect

    Volvo Trucks North America is recalling 2020 VNL vehicles because window hinges may fail if sleeper windows are open, posing a crash risk.

    Product
    VOLVO — VOLVO VNL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V607000·2020-10-02

    Mercedes-Benz Recalls 2020 GLC 350e for High-Voltage Wiring Harness Defect

    Mercedes-Benz is recalling 2020 GLC 350e hybrid vehicles because a high-voltage wiring harness shield may fail, causing an electrical malfunction and vehicle stall.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLC 350 E
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V610000·2020-10-02

    Micro Bird Recalls 2019 MB II Buses Due to Electrical Fire Risk

    Micro Bird is recalling 75 model-year 2019 MB II buses because a grounding wire issue may cause a short circuit, increasing the risk of fire.

    Product
    MICRO BIRD — MICRO BIRD MB II SCHOOL BUS, MB II TRANSIT BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20E073000·2020-10-02

    Dick's Sporting Goods Recalls Field & Stream Kayak Cradles

    Dick's Sporting Goods is recalling Field & Stream Kayak Cradles because kayaks may fall off while driving, increasing crash risk.

    Product
    EQUIPMENT recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide