The Recall Desk

State

Iowa product recalls

73,219 recalls have nationwide distribution and so reach Iowa. 5,590 additional recalls listed Iowa specifically in their distribution scope.

What the numbers show

Total
5,590
Critical
910
Severe
1,320
Most recent
2026-09-30

Of the 5,590 recalls naming Iowa we have scored against our rubric, 910 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,320 (24%) are Severe.

These figures cover only the 5,590 recalls whose distribution notice names Iowa specifically. The 73,219 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

16226–16250 of 78809

  • SevereFDA (Food)·F-1172-2023·2023-07-12

    Savory Chicken Marinade Mix Recalled for Salmonella Contamination

    Newly Weds Foods is recalling Savory Chicken Marinade Mix due to potential Salmonella contamination. The affected product was distributed across 27 US states and Canada.

    Product
    G94311 SAVORY CHICKEN MARINADE MIX X3 50.00 BAG
    Category
    Food
    Distribution
    28 states
  • SevereFDA (Food)·F-1036-2023·2023-07-12

    Breader Product Recalled Due to Possible Salmonella Contamination

    Newly Weds Foods is recalling breader product distributed across the United States and Canada due to potential Salmonella contamination. Consumers should not consume the affected product.

    Product
    A50718 BREADER X1 35.00 BAG
    Category
    Food
    Distribution
    28 states
  • SevereFDA (Food)·F-1053-2023·2023-07-12

    Newly Weds Foods Breader Recalled for Potential Salmonella Contamination

    Newly Weds Foods is recalling approximately 6.5 million pounds of breader product due to potential Salmonella contamination. The affected product was distributed across the United States and Canada.

    Product
    A91283 BREADER X2 50.00 BAG
    Category
    Food
    Distribution
    28 states
  • SevereFDA (Food)·F-1159-2023·2023-07-12

    Patty Seasoning Recalled for Potential Salmonella Contamination

    Newly Weds Foods is recalling patty seasoning due to potential Salmonella contamination. The affected product was distributed across the US and Canada.

    Product
    G83494 PATTY SEASONING #23 A X1 42.00 CASE
    Category
    Food
    Distribution
    28 states
  • SevereFDA (Food)·F-1060-2023·2023-07-12

    Newly Weds Foods Breader Product Recalled for Potential Salmonella

    Newly Weds Foods is recalling A99744 Breader product due to potential Salmonella contamination. The product was distributed across the United States and Canada.

    Product
    A99744 BREADER X1 50.00 BAG
    Category
    Food
    Distribution
    28 states
  • SevereFDA (Food)·F-1104-2023·2023-07-12

    Breader Recalled: Newly Weds Foods B94464 for Salmonella Contamination

    Newly Weds Foods is recalling approximately 6.5 million pounds of B94464 breader product due to potential Salmonella contamination. Consumers should not use this product.

    Product
    B94464 BREADER X1 50.00 BAG
    Category
    Food
    Distribution
    28 states
  • SevereFDA (Food)·F-1058-2023·2023-07-12

    Newly Weds Foods Breader Recalled Due to Salmonella Risk

    Newly Weds Foods is recalling A97176 BREADER X3 breader products that may contain Salmonella. The recall affects products with specific lot codes distributed across multiple U.S. states and Canada.

    Product
    A97176 BREADER X3 50.00 BAG
    Category
    Food
    Distribution
    28 states
  • SevereFDA (Food)·F-1214-2023·2023-07-12

    Cajun Turkey Inject Product Recalled for Potential Salmonella

    Newly Weds Foods is recalling Inject for Cajun Turkey products due to potential Salmonella contamination. The product was distributed across 27 U.S. states and Canada.

    Product
    S18149 INJECT FOR CAJUN TURKEY X1 50.00 BAG
    Category
    Food
    Distribution
    28 states
  • HighFDA (Devices)·Z-2053-2023·2023-07-12

    TrackMaster TMX428 Treadmill drive circuit board malfunction recall

    Drive board malfunction in TrackMaster TMX428 treadmills can cause unexpected belt reversal or acceleration, creating fall and impact injury risks. 376 units affected.

    Product
    TRACKMASTER, TREADMILL TMX428 220V, MODEL NUMBER 317-07927
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2081-2023·2023-07-12

    PriMatrix Ag Fenestrated dermal repair scaffolds recalled for endotoxin testing issues

    TEI Biosciences recalled 7,264 units of PriMatrix Ag Fenestrated dermal repair scaffolds nationwide due to possible out-of-specification endotoxin test results caused by testing methodology defects.

    Product
    PriMatrix Ag Fenestrated; Dermal Repair Scaffold; Rx Only; Sizes 10x25 cm, 20x25 cm, 4x4 cm, 6x6 cm, 8x12 cm, 8x8 cm.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2059-2023·2023-07-12

    Fenestrated Graspers Recalled Due to Potential Breakage and Fragment Risk

    Intuitive Surgical is recalling 46,033 da Vinci Xi/X Tip-Up Fenestrated Graspers worldwide due to a manufacturing issue that can cause grip breakage, potentially allowing stainless steel fragments to enter the patient.

    Product
    da Vinci Xi/X Tip-Up Fenestrated Grasper, REF: 470347, VER: 12
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2077-2023·2023-07-12

    PriMatrix Dermal Repair Scaffold recalled due to endotoxin testing issues

    TEI Biosciences is recalling 4,159 units of PriMatrix Dermal Repair Scaffold nationwide due to possible out-of-specification endotoxin test results. Quality control issues during testing led to this recall.

    Product
    PriMatrix; Dermal Repair Scaffold; Rx Only; Sizes 0.2x26.5 cm (3 pack), 10x12cm, 10x25 cm, 20x25 cm, 4x4 cm, 6x6 cm, 8x12 cm, and 8x8 cm.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2070-2023·2023-07-12

    Surgical collagen matrix recall due to endotoxin testing failures

    TEI Biosciences is recalling 22,163 units of SurgiMend PRS collagen matrices due to endotoxin testing deficiencies that may have resulted in contaminated products being distributed. No injuries have been reported.

    Product
    SurgiMend PRS; Collagen Matrix for Soft Tissue Reconstruction; Rx Only; Sizes 10x15 cm Semi-Oval, 7x17 cm Fenestrated, 10x20 cm Fenestrated, 8x16 cm Semi-Oval, 15x15 cm Semi-Oval, 8x20 cm Fenestrated, 10x15 cm Slant Fenestrated, 7x17 cm Semi-Oval, 8x16 cm Thin Semi-Oval, 10x20…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2063-2023·2023-07-12

    BETTA LINK SR Reusable Fishmouth Guide may bend and shed metal shavings

    T.A.G. Medical Products is recalling BETTA LINK SR Reusable Fishmouth Guides (Part Number 110045151) because the drill guides may bend during surgical use and result in metal shavings. The risk to patients includes potential injury.

    Product
    BETTA LINK SR REUSABLE FISHMOUTH GUIDE-Intended for use in soft tissue to bone fixation in the repair of the natural ligament or tendon disruption or to assist in reconstruction surgeries. Part Number: 110045151
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1013-2023·2023-07-12

    Romaine Lettuce Recalled for Potential Contamination from Deer Feces

    G.O. Corporation is recalling romaine lettuce due to potential contamination with deer feces. The recall affects lettuce distributed in Iowa, Minnesota, North Dakota, and Wisconsin with lot number 130166.

    Product
    Romaine lettuce, packaged into the following configurations and sizes: 1. Medium, Produce Code 720832, 6-2lb per shipping case. 2. Medium, Produce Code 720840, 10-2lb per shipping case. 3. 1.5XRandom, Produce Code 720625, 4-2.5lb bags per shipping case. 4.…
    Category
    Food
    Distribution
    4 states
  • HighFDA (Devices)·Z-2067-2023·2023-07-12

    LinkSymphoKnee Knee Augment Recalled for Incorrect Screw Orientation

    Waldemar Link GmbH & Co. KG recalled LinkSymphoKnee Distal Femoral Augments due to incorrect screw orientation during manufacturing. The fixation screw may be inserted through the wrong side of the augment, affecting 20 units distributed across seven US states.

    Product
    LinkSymphoKnee Distal Femoral Augment - Tilastan - Size. 7-8, Lateral-Right/Medial-Left, 5mm-Intended for primary and revision total knee replacement in skeletally mature patients. Product Code: 880-307/21
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2057-2023·2023-07-12

    TrackMaster GE Treadmill Recall Due to Drive Circuit Board Malfunction

    Full Vision Inc is recalling 1,416 TrackMaster GE T2100-ST2 220V treadmills worldwide due to a drive circuit board defect that can cause the treadmill to stop suddenly, reverse unexpectedly, or accelerate forward, posing a risk of falls or injury.

    Product
    TRACKMASTER, TREADMILL GE T2100-ST2 220V, MODEL NUMBER 317-07927GE
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·23V476000·2023-07-12

    Polestar 2 Recalled for Potential Steering Loss Due to Defective Ball Joint

    Polestar is recalling certain 2023 Polestar 2 vehicles due to a defect in the front left lower ball joint that could cause loss of steering control. Owners should contact their dealer for a free inspection and replacement.

    Product
    POLESTAR — POLESTAR POLESTAR 2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2076-2023·2023-07-12

    Collagen surgical matrix recalled for potential endotoxin testing issues

    TEI Biosciences is recalling 9,215 units of SurgiMend PRS Meshed, a surgical collagen matrix, due to possible out-of-specification endotoxin test results.

    Product
    SurgiMend PRS Meshed; Collagen Matrix for Soft Tissue Reconstruction; Rx Only; Size 10cm x 20cm
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2060-2023·2023-07-12

    BETTA LINK SR Knotless Implant Kit Drill Guides May Bend During Surgery

    The FDA has recalled BETTA LINK SR Knotless Implant Kits because the drill guides may bend during surgical procedures, potentially releasing metal shavings. This affects surgeons and patients undergoing orthopedic ligament and tendon repair procedures worldwide.

    Product
    BETTA LINK SR KNOTLESS IMPLANT KIT-Intended for use in soft tissue to bone fixation in the repair of the natural ligament or tendon disruption or to assist in reconstruction surgeries. Part Number:110045154
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2073-2023·2023-07-12

    SurgiMend MP Collagen Matrix Recalled for Endotoxin Testing Issues

    TEI Biosciences recalled approximately 3,992 units of SurgiMend MP surgical implants nationwide due to issues with endotoxin testing procedures that may have resulted in unreliable test results.

    Product
    SurgiMend MP; Collagen Matrix for Soft Tissue Reconstruction; Rx Only; Sizes 10x15 cm, 20x20 cm, 13x25 cm, 16x20 cm, 20x25 cm, 20x30 cm, and 25x40 cm.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·23V479000·2023-07-12

    BMW Recalls 2023 Models for Dashboard Control Malfunction

    BMW is recalling 2023 740i, 760i, and i7 vehicles because the dashboard Interaction Bar may fail to activate defrosting or hazard lights.

    Product
    BMW — BMW 760I, I7, 740I
    Category
    Vehicle
    Distribution
    Distributed nationwide