The Recall Desk

State

Louisiana product recalls

73,833 recalls have nationwide distribution and so reach Louisiana. 6,967 additional recalls listed Louisiana specifically in their distribution scope.

What the numbers show

Total
6,967
Critical
1,107
Severe
1,740
Most recent
2026-11-14

Of the 6,967 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 1,740 (25%) are Severe.

Which agencies issued them

These figures cover only the 6,967 recalls whose distribution notice names Louisiana specifically. The 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

54326–54350 of 80800

  • HighFDA (Devices)·Z-1348-2016·2016-04-13

    Ortho-Clinical VITROS 5600 Integrated System Recalled for Wiring Error

    Ortho-Clinical Diagnostics is recalling VITROS 5600 Integrated Systems because a wiring error may leave a module energized when the power cord is unplugged.

    Product
    VITROS 5600 Integrated System, Unique Device Identifier No. 10758750002740 & 10758750007110. Intended for use in the in vitro measurement of a variety of analytes of clinical interest.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1346-2016·2016-04-13

    AngioDynamics Recalls NAMIC Convenience Kits Due to Needle Lumen Defect

    AngioDynamics is recalling 45 NAMIC Convenience Kits because the needle inner lumen may be too small to accept a 0.038-inch guidewire.

    Product
    NAMIC CONVENIENCE KIT MERCY GENERAL HOSPITAL NEURO KIT, REF Catalog No. 601319810, UPN Product No. H7496013198101 Product Usage - This needle is intended to be placed over the guidewire to enlarge the opening in the vessel, and is then removed before sliding the catheter…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1017-2016·2016-04-13

    PerCoBa Whey Protein Isolate Recalled for Missing Milk Allergen Labeling

    Immuno-Dynamics, Inc. is recalling PerCoBa Whey Protein Isolate with Colostrum because the labels fail to state that the product contains milk.

    Product
    PerCoBa Whey Protein Isolate with Colostrum, Dietary Supplement. Net Weight: 1 kg (2.2 lbs), Colostrum 3,000 mg. UPC 90576-00009. Immuno-Dynamics, Inc., 18000 Dodge Street, Fennimore, WI 53809.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1316-2016·2016-04-13

    Recall of eValueMed Infant Heel Warmers and Transport Mattresses

    Philips is recalling eValueMed Infant Heel Warmers and Transport Mattresses because they lack expiration dates and warnings about overheating risks after shelf life.

    Product
    evaluemed Infant Heel Warmer 301-1223; Distributed by Tri-anim A disposable heel warmer for use when circulation needs to be stimulated in the infant heel in order for blood sampling to occur
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·16142·2016-04-13

    Rollerblade USA Recalls Inline Skating Helmets Due to Head Injury Hazard

    Rollerblade USA is recalling about 500 Maxxum inline skating helmets because the plastic shell can crack, causing the helmet to shift and potentially result in head injuries.

    Product
    Rollerblade inline skating helmets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1016-2016·2016-04-13

    Immuno-Dynamics Recalls PerCoBa Colostrum Supplement for Missing Milk Labeling

    Immuno-Dynamics is recalling PerCoBa and Synertek colostrum supplements because the labels fail to state that the products contain milk.

    Product
    PerCoBa 1, Colostral Whey, Dietary Supplement, Colostral Whey Protein 6.4%. Net Contents: 4 oz. Immuno-Dynamics, Inc. , PO Box 544 Perry, Iowa 50220
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·16E034000·2016-04-13

    Nitrous Outlet Recalls Nitrous Solenoid Valves Due to Welding Defect

    Nitrous Outlet is recalling specific .122 Nitrous Solenoid valves due to improper welding that may cause the piston to eject under pressure, posing an injury risk.

    Product
    FUEL SYSTEM, OTHER:DELIVERY:HOSES, LINES/PIPING, AND FITTINGS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1326-2016·2016-04-13

    Synthes Recalls Titanium Low Profile Neuro Screws Due to Thread Defect

    Synthes (USA) Products LLC is recalling specific lots of Titanium Low Profile Neuro Screws because the thread height is undersized, which may affect the device's structural integrity.

    Product
    Titanium Low Profile Neuro Screw, Self Drilling, 3mm, part numbers: 400.833, 400.833E Product Usage: The Low Profile Neuro Plating System is intended for use in selective trauma of the midface and craniofacial skeleton; craniofacial surgery; reconstructive procedures; and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1347-2016·2016-04-13

    GE Medical Systems Recalls SIGNA Pioneer MR Systems Due to Ferrous Material Risk

    GE Medical Systems is recalling 16 SIGNA Pioneer MR systems because ferrous material in the Table Control Box could cause unexpected attraction to the magnetic field during servicing, posing a risk of serious injury to personnel.

    Product
    SIGNA Pioneer MR Systems Product Usage: The SIGNA Pioneer is a whole body magnetic resonance scanner designed to support high resolution, high signal-to-noise ratio, and short scan times. It is indicated for use as a diagnostic imaging device to produce axial, sagittal…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1273-2016·2016-04-13

    Focus Diagnostics Recalls Simplexa Direct Amplification Discs for Diagnostic Errors

    Focus Diagnostics is recalling Simplexa Direct Amplification Discs because they may cause false test results or error codes.

    Product
    Simplexa Flu A/B & RSV Direct (MOL2650) with Direct Amplification Disc (MOL1451, MOL1452, MOL1455) Model Number: MOL2650, MOL1451, MOL1452, MOL1455
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1328-2016·2016-04-13

    MicroAire PAL-R4011XL Cannula Recalled Due to Breakage During Surgery

    MicroAire is recalling PAL-R4011XL cannulas because three reports indicated the devices bent or broke during surgical procedures.

    Product
    MicroAire PAL¿ Cannula Product Usage - Power Aspiration Device
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1345-2016·2016-04-13

    AngioDynamics Recalls NAMIC Convenience Kits Due to Needle Lumen Defect

    AngioDynamics is recalling 8 NAMIC Convenience Kits because the needle inner lumen is too small to accept the intended guidewire.

    Product
    NAMIC CONVENIENCE KIT HOLYOKE HOSPITAL SPECIAL PROCEDURE KIT, REF Catalog No. 60080094, UPN Product No. H749600800941 Product Usage - This needle is intended to be placed over the guidewire to enlarge the opening in the vessel, and is then removed before sliding the catheter…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1331-2016·2016-04-13

    Applied Medical Resources Recalls Epix Universal Clip Applier Kits

    Applied Medical Resources is recalling specific Epix Universal Clip Applier kits due to a potential loading mechanism nonconformance.

    Product
    STD KIT GK213, AME Standard Kit 15 Product Usage: The Epix disposable laparoscopic clip applier is indicated for ligation of tubular structures or vessels in laparoscopic and general surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1320-2016·2016-04-13

    Cardinal Health Recalls Gomco Style Circumcision Clamp Trays Due to Labeling Error

    Cardinal Health is recalling Gomco Style Circumcision Clamp Trays because two lots were labeled as containing 1.1cm clamps but actually contained 1.3cm clamps.

    Product
    Gomco Style Circumcision Clamp Trays is an instrument used to compress the foreskin of the penis during circumcision of a male infant.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1349-2016·2016-04-13

    Siemens PACS Software Recall for Incorrect Distance Measurements

    Siemens Medical Solutions is recalling 49 PACS systems because they may display incorrect distance measurements when used with certain modalities and syngo Imaging.

    Product
    A Picture Archiving and Communication System (PACS) intended to display, process, read, report, communicate, distribute, store and archive digital medical images, including digital mammography images.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0810-2016·2016-04-13

    Purdue Pharma Recalls Intermezzo Tablets for Dissolution Failures

    Purdue Pharma is recalling Intermezzo (zolpidem tartrate) sublingual tablets because they failed to meet dissolution specifications.

    Product
    Intermezzo (zolpidem tartrate) sublingual tablet 1.75 mg, CIV, 30 Ct Cartons, Rx Only. Dist by Purdue Pharma L.P., Stamford, CT 06901-3431. NDC: 59011-256-30.
    Category
    Drug
    Distribution
    8 states
  • ModerateFDA (Devices)·Z-1340-2016·2016-04-13

    Zimmer Persona Knee Implant Recalled for Box Labeling Discrepancy

    Zimmer Manufacturing B.V. is recalling specific Persona knee implants because the product information on the box differed by sides, showing conflicting part and lot numbers.

    Product
    Persona The Personalized Knee System Articular Surface Posterior Stabilized (PS) Left Height 14mm Sterile. For use in total knee arthroplasty. REF 42-5114-005-14
    Category
    Medical Device
    Distribution
    19 states
  • ModerateFDA (Food)·F-1014-2016·2016-04-13

    PerCoBa Colostrum Capsules Recalled for Incorrect Milk Allergen Labeling

    Immuno-Dynamics, Inc. is recalling PerCoBa Colostrum Capsules because the labels failed to state 'contains milk.' The product was distributed nationwide and internationally.

    Product
    PerCoBa Colostrum Capsules, Dietary Supplement, Colostrum (bovine) 1g. 120 capsules. UPC 90576-00011. Allergen statement: contains dairy. Distributed by: Immuno-Dynamics, Inc., 1800 Dodge Street, Fennimore, WI 53809.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0806-2016·2016-04-13

    Meditech Formula 3 Injection Recalled Due to Expired Active Ingredient

    Meditech Laboratories is recalling Formula 3 Injection vials because the active ingredient expired before the labeled Beyond Use Date.

    Product
    Formula 3 (Papaverine 20 mg, Phentolamine 3 mg, Atropine 0.2 mg, PGE 20 mcg/mL) Injection, 5 mL vials, Rx only, Meditech Laboratories, Inc., 3200 Polaris Ave., Suite 27, Las Vegas, NV 89102.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1015-2016·2016-04-13

    Immuno-Dynamics Recalls Colostrum Lozenges for Allergen Labeling Error

    Immuno-Dynamics, Inc. is recalling PerCoBa and Synertek colostrum lozenges because the labels state 'contains dairy' instead of 'contains milk.'

    Product
    Colostrum Lozenges, Dietary Supplement, Colostrum (Bovine) 200mg. Allergen statement: contains dairy. Packaged in the following sizes and Brand names: 1. PerCoBa, UPC 90576-00006. 100 Lozenges Distributed by: Immuno-Dynamics, Inc., Fennimore, WI 53809; 2.…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1332-2016·2016-04-13

    Applied Medical Recalls Epix Universal Clip Appliers Due to Loading Defect

    Applied Medical Resources Corp is recalling specific Epix Universal Clip Applier kits due to a potential loading mechanism nonconformance.

    Product
    STD KIT GK260, Standard Set 360 Z Product Usage: The Epix disposable laparoscopic clip applier is indicated for ligation of tubular structures or vessels in laparoscopic and general surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1329-2016·2016-04-13

    Applied Medical Recalls Epix Universal Clip Appliers Due to Loading Mechanism Defect

    Applied Medical Resources Corp is recalling CA500 Epix Universal Clip Appliers due to a potential loading mechanism nonconformance. The recall affects 1,771 units distributed in the U.S. and internationally.

    Product
    CA500 Epix Universal Clip Applier Product Usage: The Epix disposable laparoscopic clip applier is indicated for ligation of tubular structures or vessels in laparoscopic and general surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1341-2016·2016-04-13

    Zimmer Persona Knee Implant Recalled for Box Labeling Discrepancy

    Zimmer Manufacturing B.V. is recalling specific Persona knee implants because the product box displayed conflicting part and lot numbers on different sides.

    Product
    Persona The Personalized Knee System Articular Surface Posterior Stabilized (PS) Left Height 18mm Sterile For use in total knee arthroplasty. REF 42-5114-008-18
    Category
    Medical Device
    Distribution
    19 states
  • ModerateFDA (Drugs)·D-0805-2016·2016-04-13

    Meditech Formula 1 Injection Recalled Due to Expired Active Ingredient

    Meditech Laboratories is recalling 1,320 vials of Formula 1 Injection because the active ingredient expired before the labeled Beyond Use Date.

    Product
    Formula 1 (Papaverine 1.8 mg, Phentolamine 0.2 mg, Atropine 0.02 mg, PGE 18 mcg/mL) Injection, 5 mL vial, Rx only, Meditech Laboratories, Inc., 3200 Polaris Ave., Suite 27, Las Vegas, NV 89102.
    Category
    Drug
    Distribution
    Distributed nationwide