State

Maine product recalls

72,907 recalls have nationwide distribution and so reach Maine. 3,894 additional recalls listed Maine specifically in their distribution scope.

What the numbers show

Total: 3,894
Critical: 468
Severe: 791
Most recent: 2026-09-02

Of the 3,894 recalls naming Maine we have scored against our rubric, 468 (12%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 791 (20%) are Severe.

Which agencies issued them

These figures cover only the 3,894 recalls whose distribution notice names Maine specifically. The 72,907 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

1326–1350 of 76801

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 (Drugs)·D-0586-2026·2026-06-17
Zep alcohol sanitizer spray drums recalled for microbial contamination
Zep Alcohol Sanitizer Spray, ethanol 70%, in 55-gallon drums is being recalled for microbial contamination. Five drums are affected.
Product
Zep, Alcohol Sanitizer Spray, Ethanol 70%, Net Contents 55 Gallons 208 Liters, Made in USA, A Zep Inc. Brand, Distributed by: Zap Inc., 350 Joe Frank Harris Parkway, SE, Emerson, GA 30137, NDC 66949-133-85.
Category
Drug
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 (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 (Devices)·Z-2333-2026·2026-06-17
CORFLO Safety PEG kit 30-4320 contains recalled lidocaine injection
CORFLO Safety PEG Kits, catalog number 30-4320, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall. 231 kits are affected.
Product
Brand Name: CORFLO Product Name: CORFLO* Safety PEG Kit Model/Catalog Number: 30-4320
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2337-2026·2026-06-17
CORFLO Safety PEG kit 50-4320 contains recalled lidocaine injection
CORFLO Safety PEG Kits with ENFit Connector, catalog number 50-4320, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall. 49 kits affected.
Product
Product Name: CORFLO* Safety PEG Kit with ENFit¿ Connector Model/Catalog Number: 50-4320
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2323-2026·2026-06-17
TDC VELOCE 25 gauge vitrectomy cutters may have loose outer knife
TDC VELOCE 25G Two Dimensional Cutters are being recalled following an increase in complaints of a loose outer knife, including reports of it loosening during use.
Product
TDC VELOCE", 25G Two Dimensional Cutter - 20k CPM; Article Numbers: 9268.VIT25, 9311.25G01, 9311.25G02, 9311.25K01, 9311.25K02, 9311.25K03, 9625.G0201;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2409-2026·2026-06-17
Halyard drape packs shipped without undergoing validated sterilization process
Halyard Drape Packs, kit code LMDP36-01, are being recalled because sealed pouches that had not undergone validated sterilization were inadvertently distributed. 72 kits affected.
Product
Halyard, Drape Pack. Kit Code: LMDP36-01.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2413-2026·2026-06-17
Orca single use endoscope valves recalled over sticking suction buttons
Boston Scientific is removing Orca Sterile, Single Use Air/Water and Suction Valves because of a higher than anticipated occurrence of the suction button sticking. 9,750 units affected.
Product
Orca Single Use Air/Water and Suction Valves, Material Number (UPN) SUV-617-50; The Orca Air/Water Valve is intended to be used to control the air/water function on an endoscope during a GI (gastrointestinal) endoscopic procedure.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2346-2026·2026-06-17
MIC Safety 24 Fr pull PEG kits contain recalled lidocaine injection
MIC Safety PEG Kits, 24 Fr PULL, catalog number 7180-24, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall. 1,006 kits affected.
Product
Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 24 Fr PULL Model/Catalog Number: 7180-24
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-2328-2026·2026-06-17
CGuard Prime 9mm carotid stent systems may resist or fail deployment
CGuard Prime Carotid Stent Systems, 135 cm with a 9 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, 9mx40mm Model/Catalog Number: CND0940
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-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-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-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
HighFDA (Food)·H-0940-2026·2026-06-17
Park St. Deli macaroni and cheese does not declare soy
Park St. Deli Macaroni & Cheese, 20 oz, is being recalled because of undeclared soy lecithin. The action covers 58,405 cases.
Product
Park St. Deli Macaroni & Cheese, NET WT 20 OZ (1 LB 4 OZ) 567g, product packed in plastic tub and placed into paperboard sleeve. 9/20 oz packages per case.
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2407-2026·2026-06-17
Halyard pain packs shipped without validated sterilization in Iowa
Halyard Pain Packs, kit code AMPK48-01, are being recalled because sealed pouches that had not undergone validated sterilization were inadvertently distributed. 120 kits affected.
Product
Halyard, Pain Pack. Kit Code: AMPK48-01.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2399-2026·2026-06-17
Hintermann left talar implant packaging contained a right-side device
Hintermann Series Talar Implants, Left, Size 2, are being recalled because packaging and labeling for a left implant contained a right implant device. 67 units are affected.
Product
Hintermann Series Talar Implant, Left, Size 2 REF 302112
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-2317-2026·2026-06-17
GE Allia IGS Pulse systems pose shock risk to service personnel
Allia IGS Pulse angiographic X-ray systems are being recalled because an electrical cable issue could expose service personnel to electrical shock while power is on.
Product
Allia IGS Pulse angiographic X-ray system
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2327-2026·2026-06-17
CGuard Prime 9mm by 30mm carotid stents may fail deployment
CGuard Prime Carotid Stent Systems, 135 cm with a 9 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, 9mx30mm Model/Catalog Number: CND0930
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2341-2026·2026-06-17
MIC Safety 7170-14 push PEG kits contain recalled lidocaine injection
MIC Safety PEG Kits, 14 Fr PUSH OTW, catalog number 7170-14, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall. 22 kits affected.
Product
Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 14 Fr PUSH OTW Model/Catalog Number: 7170-14 Product Description: Feeding Tube Kit
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2335-2026·2026-06-17
CORFLO Safety PEG kit 30-6312 contains recalled lidocaine injection
CORFLO Safety PEG Kits, catalog number 30-6312, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall. 31 kits are affected.
Product
Product Name: CORFLO* Safety PEG Kit Model/Catalog Number: 30-6312
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2398-2026·2026-06-17
Siemens Dimension tacrolimus reagent cartridges may bias results positively
Three lots of the Siemens Dimension Tacrolimus Flex reagent cartridge are being recalled because of a potential positive bias in quality control and patient sample results.
Product
Siemens Dimension Tacrolimus Flex Reagent Cartridge (TAC), REF DF207, SMN 10700795; enzyme immunoassay
Category
Medical Device
Distribution
Distributed nationwide