State

Maine product recalls

72,971 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 72,971 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

5476–5500 of 76865

HighFDA (Devices)·Z-2442-2025·2025-09-03
Dragonfly Essentials loupe kits recalled because nickel nose pads may cause allergy
Orascoptic Dragonfly Essentials Kits are recalled because loupe nose pads containing nickel may cause an allergic reaction, following complaints. 32 kits are affected.
Product
Orascoptic Superior Visualization Dragonfly Essentials Kit ( Nose pad, a screw, lens cleaning wipe, side shields, head strap, and a screwdriver)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0577-2025·2025-09-03
Hostess Ding Dongs recalled over mold traced to malfunctioning cooler
Hostess Ding Dongs in twin packs and 10- and 16-count cartons are recalled for mold, which the firm traced to a malfunctioning cooler after customer complaints rose. 60,630 cases are affected.
Product
Hostess Ding Dongs CHOCOLATE CAKE WITH CREAMY FILLING 2.55 oz twin pack UPC 8 88109 01002 7; 10-1.28 oz carton (12.7 oz) UPC 8 88109 11061 1; 16-1.28 oz carton (20.31 oz) Individual selling unit - UPC 8 88109 01182 6 16-count selling unit - UPC 8 88109 11092 5
Category
Food
Distribution
42 states
HighFDA (Devices)·Z-2342-2025·2025-09-03
C-arm imaging systems recalled over missing lead tape in collimator covers
GE HealthCare OEC 9800 and OEC 9900 Elite C-arm systems are recalled because impacted units are missing the full layer of lead tape in the collimator covers, slightly increasing radiation exposure.
Product
GE HealthCare OEC 9900 Elite C-arm Systems.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2441-2025·2025-09-03
Custom loupes with Phantom frames recalled over nickel nose pad allergy risk
Orascoptic custom loupes configured with Phantom frames are recalled because loupe nose pads containing nickel may cause an allergic reaction, following complaints. 10,611 units are affected.
Product
Orascoptic Superior Visualization Custom loupes configured with Phantom Frames
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2444-2025·2025-09-03
Loupe nose pad kits recalled because nickel content may cause allergic reaction
Orascoptic Dragonfly Nose Pad Accessory Kits are recalled because loupe nose pads containing nickel may cause an allergic reaction, following complaints. 743 kits are affected.
Product
Orascoptic Superior Visualization Dragonfly Nose Pad Accessory Kit ( nose pad and screw) 1 pk and 20 pk.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0534-2025·2025-09-03
Everything bagel mix recalled because label omits sesame and other ingredients
Baker's Authority Everything Bagel Mix in 1 lb and 5 lb bags is recalled because the label does not list its ingredients, including the major food allergen sesame. 197 units are affected.
Product
Baker's Authority Everything Bagel Mix; 5lb bag and 1lb bag; stored dry at room temperature; packaged in silver bag
Category
Food
Distribution
17 states
HighNHTSA·25E054000·2025-09-03
Magna Recalls Rearview Cameras on Ford and Chrysler Vehicles
Magna International is recalling rearview cameras installed on certain Ford and Chrysler vehicles because they may display a blank or inverted image, increasing crash risk.
Product
BACK OVER PREVENTION: SENSING SYSTEM: CAMERA recall
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2423-2025·2025-09-03
Limb salvage canal filling stems recalled after unidentified substance found on devices
ELEOS Bowed Canal Filling Stems are recalled because an unidentified substance of unknown impact was found on devices during a retrospective evaluation. 30 units are affected.
Product
ELEOS SEGMENTAL LIMB SALVAGE SYSTEM, ELEOS BOWED CANAL FILLING STEMS. Canal filling stem implants.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2420-2025·2025-09-03
Operating tables recalled because interference can leave them unresponsive to controls
Corin Operating Tables are recalled because interference, such as from high-frequency surgical equipment used at the same time, can leave the table unresponsive to both the remote control and the override panel.
Product
Corin Operating Tables Model Numbers: (1) 770001A0, (2) 770001A2, (3) 770001B0, (4) 770001B2, (5) 770001F0, (6) 770001F2; All Software Versions.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·25V572000·2025-09-03
Ford Recalls Vehicles Due to Rearview Camera Display Issues
Ford is recalling specific 2015-2019 vehicles because the rearview camera may display a distorted, inverted, or blank image, increasing crash risk.
Product
FORD — FORD, LINCOLN F-450 SD, MUSTANG, EDGE, F-250 SD
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2443-2025·2025-09-03
Phantom Essential loupe kits recalled because nickel nose pads may cause allergy
Orascoptic Phantom Essential Kits are recalled because loupe nose pads containing nickel may cause an allergic reaction, following complaints. 74 kits are affected.
Product
Orascoptic Superior Visualization Phantom Essential kit ( Nose pad, a screw, lens cleaning wipe, side shields, head strap, and a screwdriver)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0604-2025·2025-09-03
Good Neighbor alcohol prep pads recalled for alcohol below labeled concentration
Good Neighbor Pharmacy Alcohol Prep Pads, distributed by AmerisourceBergen, are recalled nationwide because isopropyl alcohol levels fall below the labeled concentration. 66,000 pads are affected.
Product
GOOD NEIGHBOR PHARMACY ALCOHOL ANTISEPTIC SKIN CLEANSER — GOOD NEIGHBOR PHARMACY ALCOHOL ANTISEPTIC SKIN CLEANSER (ISOPROPYL ALCOHOL)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2425-2025·2025-09-03
Limb salvage stem extensions recalled after unidentified substance found on devices
ELEOS Segmental Limb Salvage System straight splined slotted stem extensions are recalled because an unidentified substance of unknown impact was found on devices during a retrospective evaluation. 554 units are affected.
Product
ELEOS SEGMENTAL LIMB SALVAGE SYSTEM, ELEOS STEM EXTENSION, STRAIGHT, SPLINED, SLOTTED. Canal filling stem implants.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2440-2025·2025-09-03
Custom loupes with Dragonfly frames recalled over nickel nose pad allergy risk
Orascoptic custom loupes with Dragonfly frames are recalled because loupe nose pads containing nickel may cause an allergic reaction, following complaints. 15,245 units are affected.
Product
Orascoptic Superior Visualization Custom loupes with Dragonfly frames
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·25V570000·2025-09-03
Ducati Motorcycles Recalled for Defective Rear Wheel Axle
Ducati is recalling certain 2018-2025 motorcycles because the rear wheel axle may lose structural integrity and break during riding, risking loss of control. Dealers will replace the axle free of charge.
Product
DUCATI — DUCATI STREETFIGHTER, STREETFIGHTER V2, PANIGALE V4 S, STREETFIGHTER V4
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2462-2025·2025-09-03
Foley catheters recalled because obstructed lumen may prevent bladder drainage
Bardex Lubri-Sil I.C. Foley catheters and related tray systems are recalled because the catheter may have an obstructed lumen, which may prevent the bladder from draining. 175,158 units are affected.
Product
Bardex Lubri-Sil I.C. 400-series Temperature Sensing Silver/Hydrogel Coated All-Silicone Foley Catheter 5cc Balloon, REF: 119314; SureStep Foley Tray System Lubri-Sil I.C. Complete Care, REF: A319514A; Bard Silver Lubri-Sil Foley Tray Temperature Sensing with Bard Hydrogel and
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2424-2025·2025-09-03
Canal filling stems recalled after unidentified substance found during retrospective evaluation
ELEOS Segmental Stem Canal Filling straight slotted splined 2/3 plasma implants are recalled because an unidentified substance of unknown impact was found on devices. 15 units are affected.
Product
ELEOS SEGMENTAL LIMB SALVAGE SYSTEM, ELEOS SEGMENTAL STEM CANAL FILLING STRAIGHT SLOTTED SPLINED 2/3 PLASMA. Canal filling stem implants.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0598-2025·2025-09-03
Sucralfate tablets recalled after bankruptcy left quality program unmonitored
Sucralfate Tablets USP 1 gram from American Health Packaging are recalled because the firm's Chapter 11 filing left it unable to monitor its quality program. 26,992 blister packs are affected.
Product
Sucralfate Tablets, USP 1 gram, 100 Tablets, (10x10), Rx Only, Distributed by: American Health Packaging, Columbus, Ohio 43217 NDC 60687-695-01 - Carton NDC [60687-695-11- Unit Dose]
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0600-2025·2025-09-03
Medline alcohol prep pads recalled for alcohol below labeled concentration
Medline Alcohol Prep Pads, 70% isopropyl alcohol, are recalled nationwide because isopropyl alcohol levels fall below the labeled concentration. The recall covers 6,669,874 swabs.
Product
MEDLINE ALCOHOL PREP — MEDLINE ALCOHOL PREP (ISOPROPYL ALCOHOL)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·H-0535-2025·2025-09-03
Graham cracker meal recalled because label lists no ingredients or allergens
Baker's Authority Graham Cracker Meal in 5 lb bags is recalled because the label does not list its ingredients, including the major food allergens wheat and soy. 70 units are affected.
Product
Baker's Authority Graham Cracker Meal; 5lb bag; stored dry at room temperature; packaged in silver bag
Category
Food
Distribution
17 states
HighFDA (Drugs)·D-0599-2025·2025-09-03
Lisdexamfetamine 40 mg bottles recalled after being filled with 30 mg capsules
Lisdexamfetamine Dimesylate Capsules 40 mg, lot 25280726A, distributed by Lannett, are recalled because a bottle labeled 40 mg contained 30 mg capsules. 8,544 bottles are affected.
Product
LISDEXAMFETAMINE DIMESYLATE — LISDEXAMFETAMINE DIMESYLATE (LISDEXAMFETAMINE DIMESYLATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2477-2025·2025-09-03
Medication dispensing stations recalled because antivirus software was not consistently installed
BD Pyxis MedStation and Anesthesia Station devices are recalled because antivirus software was not consistently installed during implementation. 8,353 devices are affected, 6,738 of them in the US.
Product
BD Pyxis Product Name / UDI-DI code / Catalog No. BD Pyxis" MedStation" 4000 Main / 10885403512629 / 303 BD Pyxis" MedStation" ES Tower / 10885403512674 / 352 BD Pyxis" Anesthesia Station ES / 10885403477836 / 327 BD Pyxis" MedStation" ES (Main) / 10885403512667 / 323
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2417-2025·2025-09-03
NovoTHOR XL devices recalled over failed welded nut detaching gas strut
NovoTHOR XL devices, model S2190, are recalled because a failed welded nut may shear off, detaching a gas strut from the canopy and making the canopy difficult to lift. 55 units are affected.
Product
Brand Name: THOR Product Name: NovoTHOR XL Model/Catalog Number: S2190 Software Version: N/A Product Description: The NovoTHOR and NovoTHOR XL are intended to emit energy in the visible and IR spectrum to provide topical heating for the purpose of elevating tissue temperature
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2421-2025·2025-09-03
Dental implant locating kits recalled over thread defect limiting full engagement
Atlantis IO FLO-S Kits are recalled because a thread defect stops the device fully engaging an implant or analog, engaging about two rotations instead of five. 102 units are affected.
Product
Brand Name: Atlantis IO FLO-S Product Name: Atlantis IO FLO-S Kit Model/Catalog Number: A04B / 68020033 Software Version: n/a Product Description: The Atlantis intraoral feature locating object for suprastructures (IO FLO-S) is intended to support the prosthetic procedure wit
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2475-2025·2025-09-03
Anti-Xa test kits recalled over potential contamination by fibrinogen reagents
STA-Liquid Anti-Xa 8 kits are recalled because of the potential for contamination by Stago Fibrinogen reagents in unfractionated and low molecular weight heparin applications. 126,200 units are affected.
Product
STA-Liquid Anti-Xa 8. Model/Catalog Number: 00322US. The STA - Liquid Anti-Xa kits are intended for use with STA-R, STA Compact and STA Satellite analyzers, for the quantitative determination of the plasma levels of unfractionated (UFH) and low molecular weight (LMWH) heparin
Category
Medical Device
Distribution
Distributed nationwide