State

Iowa product recalls

72,907 recalls have nationwide distribution and so reach Iowa. 5,581 additional recalls listed Iowa specifically in their distribution scope.

What the numbers show

Total: 5,581
Critical: 909
Severe: 1,317
Most recent: 2026-09-09

Of the 5,581 recalls naming Iowa we have scored against our rubric, 909 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,317 (24%) are Severe.

Which agencies issued them

These figures cover only the 5,581 recalls whose distribution notice names Iowa specifically. The 72,907 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

1351–1375 of 78488

HighFDA (Devices)·Z-2351-2026·2026-06-17
MIC Safety 20 Fr PEG kits contain recalled lidocaine injection
MIC Safety PEG Kits with ENFit Connectors, 20 Fr PULL, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall for quality issues. 6,005 kits affected.
Product
Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors 20 Fr PULL Model/Catalog Number: 8180-20
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2315-2026·2026-06-17
GE Allia IGS 5 Pulse systems pose shock risk to servicers
Allia IGS 5 Pulse angiographic X-ray systems are being recalled because an electrical cable issue could expose service personnel to electrical shock while power is on. 121 units affected.
Product
Allia IGS 5 Pulse angiographic X-ray system
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2321-2026·2026-06-17
Bicarby dialysate luer-lock connections may leak fluid onto floors
Bicarby Dialysate across six model numbers is being recalled because luer-lock leaks during preparation present a potential slip and fall hazard from fluid on the floor.
Product
Bicarby" Dialysate; Model Numbers: RFP-400-G, RFP-401-G, RFP-402-G, RFP-404-G, RFP-407-G, and RFP-456-G;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2347-2026·2026-06-17
MIC Safety 14 Fr push PEG kits contain recalled lidocaine injection
MIC Safety PEG Kits with ENFit Connectors, 14 Fr PUSH OTW, catalog number 8170-14, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall.
Product
Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors 14 Fr PUSH OTW Model/Catalog Number: 8170-14 Product Description: Feeding Tube Kit Component: No
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2349-2026·2026-06-17
MIC Safety 24 Fr push OTW PEG kits contain recalled lidocaine
MIC Safety PEG Kits with ENFit Connectors, 24 Fr PUSH OTW, catalog number 8170-24, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall.
Product
Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors 24 Fr PUSH OTW Model/Catalog Number: 8170-24
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0607-2026·2026-06-17
Budesonide inhalation ampules contain black and brown specks and particles
Budesonide Inhalation Suspension, 1 mg/2 mL single-dose ampules from Sun Pharmaceutical, is being recalled after a quality complaint of black or brown specs and particles in the solution.
Product
BUDESONIDE — BUDESONIDE (BUDESONIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2312-2026·2026-06-17
Plum Duo infusion pumps may not display soft limit alerts
Plum Duo Infusion Pumps are being recalled because under certain conditions the pump may not display a soft limit alert before delivery starts, potentially leading to under- or over-delivery.
Product
Plum Duo Infusion Pump, 40002-0401
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2405-2026·2026-06-17
Abbott Merlin pacemaker programmer may fail to terminate threshold test
Merlin Patient Care System programmer software is being recalled because a malfunction during a pacing capture threshold test may stop the command to terminate the test being communicated.
Product
Merlin" Patient Care System (PCS) software Merlin" PCS 3650 programmer Model 3330 software
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2316-2026·2026-06-17
GE Allia IGS 7 Pulse systems pose shock risk to servicers
Allia IGS 7 Pulse angiographic X-ray systems are being recalled because an electrical cable issue could expose service personnel to electrical shock while power is on. 35 units affected.
Product
Allia IGS 7 Pulse angiographic X-ray system
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2345-2026·2026-06-17
MIC Safety 20 Fr pull PEG kits contain recalled lidocaine injection
MIC Safety PEG Kits, 20 Fr PULL, catalog number 7180-20, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall. 3,184 kits affected.
Product
Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 20 Fr PULL Model/Catalog Number: 7180-20
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2400-2026·2026-06-17
Aluminum chloride hemostatic gel kits shipped with wrong package insert
Advance Aluminum Chloride Gel Clear Hemostatic Gel Kits are being recalled because some units contain the package insert for Ferric Sulfate Gel, which gives different first aid instructions.
Product
Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit, Catalog number 504600-28
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2330-2026·2026-06-17
CGuard Prime 10mm by 40mm carotid stents may fail deployment
CGuard Prime Carotid Stent Systems, 135 cm with a 10 mm x 40 mm stent, are being recalled because the delivery system may meet high resistance or fail to deploy the stent.
Product
CGuard¿ Prime Carotid Stent System, 135cm, 10mmx40mm Model/Catalog Number: CND1040
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2350-2026·2026-06-17
MIC Safety 14 Fr PEG kits contain recalled lidocaine injection
MIC Safety PEG Kits with ENFit Connectors, 14 Fr PULL, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall for quality issues.
Product
Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors 14 Fr PULL Model/Catalog Number: 8180-14
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2356-2026·2026-06-17
NexxZr dental zirconia discs may have reduced or missing dentin layer
NexxZr T Multi A3.5 zirconia discs for all-ceramic dental restorations are being recalled because a reduced or missing dentin layer increases the risk of fracture in the mouth.
Product
NexxZr T Multi A3.5 W98-16mm, REF: 745451
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0912-2026·2026-06-17
Farm Rich Pizza Cheese Crunchers may contain metal pieces
Farm Rich Pizza Cheese Crunchers from Rich Products Corp are being recalled because they may contain metal pieces. The action covers 6,408 cases, or 160,200 lbs.
Product
Farm Rich Pizza Cheese Crunchers
Category
Food
Distribution
21 states
HighFDA (Devices)·Z-2329-2026·2026-06-17
CGuard Prime 10mm by 30mm carotid stents may fail deployment
CGuard Prime Carotid Stent Systems, 135 cm with a 10 mm x 30 mm stent, are being recalled because the delivery system may meet high resistance or fail to deploy the stent.
Product
CGuard Prime Carotid Stent System, 135cm, 10mmx30mm Model/Catalog Number: CND1030
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2325-2026·2026-06-17
CGuard Prime 8mm by 30mm carotid stents may fail deployment
CGuard Prime Carotid Stent Systems, 135 cm with an 8 mm x 30 mm stent, are being recalled because the delivery system may meet high resistance or fail to deploy the stent.
Product
Brand Name: CGuard¿ Prime Carotid Stent System, 135cm, 8mmx30mm Model/Catalog Number: CND0830
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2313-2026·2026-06-17
Plum Duo Precision IV pumps may not display soft limit alerts
Plum Duo Precision IV Pumps are being recalled because under certain conditions the pump may not display a soft limit alert before delivery starts, potentially leading to under- or over-delivery.
Product
Plum Duo Precision IV Pump, 40002-0403
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2343-2026·2026-06-17
MIC Safety 24 Fr push PEG kits contain recalled lidocaine injection
MIC Safety PEG Kits, 24 Fr PUSH OTW, catalog number 7170-24, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall. 132 kits affected.
Product
Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 24 Fr PUSH OTW Model/Catalog Number: 7170-24 Product Description: Feeding Tube Kit Component: No
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2406-2026·2026-06-17
MOSAIQ oncology software may fail to load adapted treatment plan
The MOSAIQ Oncology Information System is being recalled because the software may fail to load an adapted baseline shift plan during treatment delivery when a communication error occurs.
Product
MOSAIQ Oncology Information System
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2326-2026·2026-06-17
CGuard Prime 8mm carotid stent systems may resist or fail deployment
CGuard Prime Carotid Stent Systems, 135 cm with an 8 mm x 40 mm stent, are being recalled because the delivery system may meet high resistance or fail to deploy the stent.
Product
Brand Name: CGuard¿ Prime Carotid Stent System, 135cm, 8mmx40mm Model/Catalog Number: CND0840
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2348-2026·2026-06-17
MIC Safety 20 Fr push OTW PEG kits contain recalled lidocaine
MIC Safety PEG Kits with ENFit Connectors, 20 Fr PUSH OTW, catalog number 8170-20, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall.
Product
Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors 20 Fr PUSH OTW Model/Catalog Number: 8170-20
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2404-2026·2026-06-17
Boston Scientific Clik X anchors may lack sterility assurance
Boston Scientific Clik X Anchors, model SC-4318, are being recalled because the sterile anchors may lack sterility assurance. 43 units are affected.
Product
Boston Scientific Model SC-4318, Clik X Anchor REF: M365SC43180
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2361-2026·2026-06-17
Medartis APTUS compression screws have off-centre cannulation in affected lots
Medartis APTUS 5.0 headed cannulated compression screws for bone fixation are being recalled because the cannulation of the screw is not centered. 13 units are affected.
Product
Medartis APTUS, 5.0 headedCCS Long Thread 50/20mm, REF A-8216.50/1, 1/Pkg; Cannulated Compression Screws for bone fixation
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2311-2026·2026-06-17
Plum Solo Precision IV pumps may not display soft limit alerts
Plum Solo Precision IV Pumps are being recalled because under certain conditions the pump may not display a soft limit alert before delivery starts, potentially leading to under- or over-delivery.
Product
Plum Solo Precision IV Pump, 40001-0401
Category
Medical Device
Distribution
Distributed nationwide