Archive
804 recalls were announced in October 2025.
Of the 804 recalls this month scored against our rubric, 22% are Critical, 10% are Severe.
Which agencies issued them
GE HealthCare is recalling 82 Millenium Myosight gamma cameras because systems past guaranteed service may have been moved without adequate detector support, risking a detector fall.
HeartSine Technologies is recalling 1,291,165 Pad-Pak units because defibrillator pads may contain damaged pins that disrupt the mechanical fit and electrical contact.
Rolling Pin Baking Company is recalling 127,680 units of Rolling Pin Dubai Style Chocolate because the product does not declare wheat in the allergen statement.
GE HealthCare is recalling 64 Elscint Model 4XX gamma cameras because systems past guaranteed service may have been moved without adequate detector support, risking a detector fall.
Tandem Diabetes Care is recalling 122,958 t:slim X2 and Mobi insulin pumps because a software defect when paired with a Dexcom G7 sensor may trigger an unexpected automatic correction bolus.
Becton Dickinson is recalling 2,050 BD EpiCenter Microbiology Data Management Systems after product service credentials used by some technical support teams were accessed by an unauthorized actor.
Mars Foods US is recalling 1,075 cases of Ben's Original Ready Rice Long Grain & Wild because of the possible presence of stones in the product.
Beckman Coulter is recalling 571 DxI 9000 Access Immunoassay Analyzers over a software anomaly that may not apply user-specified manual dilution factors, risking false low or high results.
GE HealthCare is recalling one Optima NX gamma camera because systems past guaranteed service may have been moved without adequate detector support, risking a detector fall.
Southwind Foods is recalling Tovala branded frozen raw phosphate free shrimp in 5 oz bags because it may have been contaminated with Cesium-137.
Georgia Nut Co is recalling 76,121 cases of tru fru Strawberries + Creme Freeze-Dried Fresh because of the potential for metal in the product.
Leprino Foods is recalling 5,453,442 lbs of bulk mozzarella slabs because of possible stainless steel pieces in the product.
Mars Foods US is recalling 315 cases of Ben's Original Ready Rice Whole Grain Brown because of the possible presence of stones in the product.
Prevost is recalling 2025 X3-45 Commuter buses because improperly installed wheelchair seat belt anchorages may detach in a crash, increasing injury risk.
MG Foods is recalling 117 Jumbo Meat Ball Subs because the mozzarella cheese ingredient has the potential to be contaminated with metal shavings.
Mars Foods US is recalling 273 cases of Ben's Original Ready Rice Original Long Grain White because of the possible presence of stones in the product.
Del Mar Food Products is recalling 966 cases of Organic IQF Chopped Spinach in 35 lb packs for potential contamination with Listeria monocytogenes.
GE HealthCare is recalling 54 Millenium MPS gamma cameras because systems past guaranteed service may have been moved without adequate detector support, risking a detector fall.
Cardinal Health is recalling all lots of ENFit Salem Sump PVC tubes after complaints of anti-reflux valve breakage due to excessive force during use.
GE HealthCare is recalling 102 Starcam and Camstar gamma cameras because systems past guaranteed service may have been moved without adequate detector support, risking a detector fall.
Medline is recalling 222,800 alcohol prep pads from one lot because the product is subpotent.
Cardinal Health is recalling all lots of Salem Sump dual lumen stomach tubes after complaints of anti-reflux valve breakage due to excessive force during use.
Georgia Nut Co is recalling 170,993 cases of tru fru Dark + White Chocolate Freeze-Dried Strawberries because of the potential for metal in the product.
GE HealthCare is recalling 2,306 Carescape Central Stations running software V3.0.5 because the system can enter a continuous reboot cycle, losing central monitoring of connected patients.
Becton Dickinson is recalling 62 BD MAX System instruments after product service credentials used by some technical support teams were accessed by an unauthorized actor.
GE is recalling 29,225 MAC VU360 acquisition trunk cables and module holders because incorrect placement of the module can wear the cable until it overheats in use.
Sedecal is recalling the SHIMADZU RF.004 mobile X-ray system, serial 75723, after emailing consignees to remind users that the equipment is not water-resistant.
JB Chemicals is recalling 13,440 bottles of Cetirizine Hydrochloride Tablets USP 10 mg because the tablets were imprinted with the wrong identification code.
Sedecal is recalling one SM_40HF_BDC3 mobile X-ray system after emailing consignees to remind users that the equipment is not water-resistant.
UIH Technologies is recalling two uCT 780 computed tomography systems because third-party outer covers can become trapped between the patient table and gantry.
Sedecal is recalling one SM-20HF-Batt 20KW analog mobile X-ray system after emailing consignees to remind users that the equipment is not water-resistant.
Sedecal is recalling one mobile X-ray system after emailing consignees to remind users that the equipment is not water-resistant and must be cleaned strictly per the manual.
Graviti Pharmaceuticals is recalling 46,512 bottles of Bupropion Hydrochloride Extended-Release Tablets USP (XL) 300 mg from one batch for failed tablet specifications.
UIH Technologies is recalling 11 uCT 760 computed tomography systems because third-party outer covers can become trapped between the patient table and gantry.
Synthes is recalling 122 low profile locking screws because 42mm screws were packaged and labeled as 46mm and 46mm screws were labeled as 42mm, though the etched length is correct.
Sedecal is recalling 56 SM-40HF-B-D-KM (AeroDR X30) mobile digital diagnostic X-ray systems after emailing consignees to remind users that the equipment is not water-resistant.
Sedecal is recalling one 40KW-FX.899 mobile X-ray system after emailing consignees to remind users that the equipment is not water-resistant.
Sedecal is recalling one SM-40HF-B-D-C 40KW 55C/60C mobile X-ray system after emailing consignees to remind users that the equipment is not water-resistant.
UIH Technologies is recalling two uCT ATLAS computed tomography systems because third-party outer covers can become trapped between the patient table and gantry.
ibspot is recalling three boxes of Taoscare Motion Sickness Patches because the product was marketed without an approved new drug application.
Sedecal is recalling eight model 40KWFXPLUS.002 mobile X-ray systems after emailing consignees to remind users that the equipment is not water-resistant.
Lannett is recalling 46,848 bottles of Niacin Extended-release Tablets USP 1,000 mg across several lots for failed dissolution specifications.
Sedecal is recalling six SM-40HF-B-D-C 40KW.002 mobile X-ray systems after emailing consignees to remind users that the equipment is not water-resistant.
JB Chemicals is recalling 9,936 hundred-count bottles of Cetirizine Hydrochloride Tablets USP 10 mg because the tablets were imprinted with the wrong identification code.
Sedecal is recalling 17 SM_40HF_B_D_VIR3 mobile X-ray systems after emailing consignees to remind users that the equipment is not water-resistant.
Sedecal is recalling five SM-40HF-B-D-C 40KW 55C mobile X-ray systems after emailing consignees to remind users that the equipment is not water-resistant.
Sedecal is recalling six 40KW70CDEMO.005 mobile X-ray systems after emailing consignees to remind users that the equipment is not water-resistant.
Sedecal is recalling six SM-40HF-B-D-C 40KW 80C mobile X-ray systems after emailing consignees to remind users that the equipment is not water-resistant.
Sedecal is recalling one SM-40HF-B-D-C 40KW Canon Ready mobile X-ray system, serial G41234, after emailing consignees to remind users that the equipment is not water-resistant.
Sedecal is recalling the SED URS LP mobile X-ray system, serial 40116, after emailing consignees to remind users that the equipment is not water-resistant.
Sedecal is recalling one SM_40HF_BDC mobile X-ray system after emailing consignees to remind users that the equipment is not water-resistant.
Sedecal is recalling one 40KWMOBILE3.899 mobile X-ray system after emailing consignees to remind users that the equipment is not water-resistant.
Sedecal is recalling one SM-40HF-B-D-C 40KW 55C mobile X-ray system, serial G37528, after emailing consignees to remind users that the equipment is not water-resistant.
Sedecal is recalling 268 model 40KWFXPLUS mobile X-ray systems after emailing consignees to remind users that the equipment is not water-resistant.
UIH Technologies is recalling 22 uCT 550 computed tomography systems because third-party outer covers can become trapped between the patient table and gantry.
Sedecal is recalling one SM-40HF-B-D-C 40KW 55C mobile X-ray system, serial G37587, after emailing consignees to remind users that the equipment is not water-resistant.
Sedecal is recalling one SM-40HF-B-D-C 40KW Canon Ready mobile X-ray system after emailing consignees to remind users that the equipment is not water-resistant.
Sedecal is recalling 12 mobile X-ray systems after emailing consignees to remind users that the equipment is not water-resistant and must be cleaned strictly per the manual.
Sedecal is recalling three model 40KWFXPLUS.004 mobile X-ray systems after emailing consignees to remind users that the equipment is not water-resistant.
Sedecal is recalling nine SM-40HF-Batt 40KW analog mobile X-ray systems after emailing consignees to remind users that the equipment is not water-resistant.
Sedecal is recalling 1,198 MobileDiagnost wDR 2.2 mobile X-ray systems after emailing consignees to remind users that the equipment is not water-resistant.
Sedecal is recalling two SM-40HF-B-D-C 40KW 55G/60G mobile X-ray systems after emailing consignees to remind users that the equipment is not water-resistant.
Church & Dwight is recalling 21,912 bottles of Zicam Medicated Fruit Drops Elderberry Flavor because the label failed to list elderberry as an ingredient.
Sedecal is recalling four SM-40HF-B-D-C 40KW 50C mobile X-ray systems after emailing consignees to remind users that the equipment is not water-resistant.
Sedecal is recalling 27 SM-40HF-B-D-C 40KW 50G mobile X-ray systems after emailing consignees to remind users that the equipment is not water-resistant.
Sedecal is recalling 22 SM-32HF-Batt 32KW analog mobile X-ray systems after emailing consignees to remind users that the equipment is not water-resistant.
UIH Technologies is recalling eight uCT 530 computed tomography systems because third-party outer covers can become trapped between the patient table and gantry.
UIH Technologies is recalling four uMI Panorama 35 PET/CT systems because third-party outer covers can become trapped between the patient table and gantry.
Sedecal is recalling 24 RadPro Mobile X-ray systems after emailing consignees to remind users that the equipment is not water-resistant.
Sedecal is recalling four SM-40HF-B-D-C 40KW 55C/60C mobile X-ray systems after emailing consignees to remind users that the equipment is not water-resistant.
Sedecal is recalling eight SM-32HF-B-D-C 32KW 50G mobile X-ray systems after emailing consignees to remind users that the equipment is not water-resistant.
Sedecal is recalling 55 model 40KWFX mobile X-ray systems after emailing consignees to remind users that the equipment is not water-resistant.
The Harvard Drug Group is recalling Gabapentin Capsules USP 100 mg in 10-capsule blister packs after routine stability testing returned an out-of-specification result for highest unknown impurity.
Sedecal is recalling 12 model 40KWFXPLUS.005 mobile X-ray systems after emailing consignees to remind users that the equipment is not water-resistant.
Synthes is recalling 120 low profile locking screws because 42mm screws were packaged and labeled as 46mm and 46mm screws were labeled as 42mm, though the etched length is correct.
Sedecal is recalling five SM-40HF-B-D-C 40KW 55G mobile X-ray systems after emailing consignees to remind users that the equipment is not water-resistant.
USV Private Limited is recalling 8,952 bottles of Olopatadine Hydrochloride Ophthalmic Solution USP 0.1% after an unspecified impurity exceeded the specification limit.
Sedecal is recalling seven model 40KWFXPLUS-710CW.007 mobile X-ray systems after emailing consignees to remind users that the equipment is not water-resistant.
Sedecal is recalling three SM_40HF_B_D_VIR3.004 mobile X-ray systems after emailing consignees to remind users that the equipment is not water-resistant.
Sedecal is recalling 181 SM-40HF-B-D-C 40KW 70C mobile X-ray systems after emailing consignees to remind users that the equipment is not water-resistant.
Sedecal is recalling one SM-40HF-B-D-C 40KW 70C EN mobile X-ray system after emailing consignees to remind users that the equipment is not water-resistant.
Sedecal is recalling 39 SM-40HF-B-D-C 40KW 50G mobile X-ray systems after emailing consignees to remind users that the equipment is not water-resistant.
Sedecal is recalling 14 SM-40HF-B-D-C 40KW 70C mobile X-ray systems after emailing consignees to remind users that the equipment is not water-resistant.
UIH Technologies is recalling three uMI 780 PET/CT systems because third-party outer covers can become trapped between the patient table and gantry.
CPM Medical Consultants is updating the Fuse ULTRA Foot Plating System instructions for use to remove a sterilization option that does not apply in the United States.
Sedecal is recalling six SM-40HF-B-D-C 40KW Canon Ready mobile X-ray systems after emailing consignees to remind users that the equipment is not water-resistant.
LeMaitre Vascular is recalling one Artegraft Collagen Vascular Graft that was incorrectly packed in outer packaging labeled for a different size.
Sedecal is recalling eight Easy Moving Plus SM-50HF-B-D-C 50KW 50G mobile X-ray systems after emailing consignees to remind users that the equipment is not water-resistant.
Sedecal is recalling six SM-40HF-B-D-C 40KW.005 mobile X-ray systems after emailing consignees to remind users that the equipment is not water-resistant.
Sedecal is recalling 142 SM-40HF-B-D-C 40KW mobile X-ray systems after emailing consignees to remind users that the equipment is not water-resistant.
UIH Technologies is recalling two uEXPLORER PET/CT systems because third-party outer covers can become trapped between the patient table and gantry, causing mechanical interference.
Sedecal is recalling 10 mobile X-ray systems after emailing consignees to remind users that the equipment is not water-resistant and must be cleaned strictly per the manual.
UIH Technologies is recalling 95 uMI 550 PET/CT systems because third-party outer covers can become trapped between the patient table and gantry.
The Harvard Drug Group is recalling Gabapentin Capsules USP 100 mg across several lots after routine stability testing returned an out-of-specification result for highest unknown impurity.
Home Health US is recalling 4,661 One Step Sterile Lancets because of incorrect or missing Unique Device Identifier codes.
Jayco is recalling certain 2025-2026 Entegra Condor and Jayco Granite Ridge motorhomes because the certification label may have the front and rear axle information reversed.
Tesla is recalling certain 2024 Cybertruck vehicles fitted with a service-installed off-road light bar because an incorrect surface primer may allow the light bar to loosen and detach.
E.A. Sween Company is recalling approximately 127,887 pounds of pulled pork sandwiches that may contain pieces of plastic. The products were distributed nationwide.
Hormel Foods is recalling about 4.8 million pounds of frozen ready-to-eat chicken products that may contain metal pieces.
Ford is recalling certain 2021-2023 Expedition, Navigator, F-150 and Super Duty vehicles because the moonroof wind deflector clips may be inadequately attached, letting the deflector detach.
Looking for a different month? Back to 2025.