State

Massachusetts product recalls

73,509 recalls have nationwide distribution and so reach Massachusetts. 8,241 additional recalls listed Massachusetts specifically in their distribution scope.

What the numbers show

Total: 8,241
Critical: 1,181
Severe: 2,353
Most recent: 2026-10-14

Of the 8,241 recalls naming Massachusetts we have scored against our rubric, 1,181 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,353 (29%) are Severe.

Which agencies issued them

These figures cover only the 8,241 recalls whose distribution notice names Massachusetts specifically. The 73,509 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

23251–23275 of 81750

SevereFDA (Drugs)·D-0782-2022·2022-04-27
artnaturals Hand Sanitizer Recalled for Benzene and Chemical Contamination
artnaturals ethyl alcohol hand sanitizer (8 fl oz bottles, lot G20127E and G20128A, exp. 5/1/2022) is recalled nationwide due to chemical contamination including benzene, acetaldehyde, and acetal.
Product
artnaturals hand sanitizer, SCENT FREE HAND SANITIZER (ethyl alcohol 62.5%), 8 fl oz (236 ml) bottles, Dist. By artnaturals, Gardena, CA 90248, UPC: 8 16820 02820 5
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0785-2022·2022-04-27
FDA Recalls Pink Pussycat Sensual Enhancement Capsules for Undeclared Sildenafil
Pink Pussycat Sensual Enhancement capsules are being recalled nationwide. The FDA found they contain undeclared sildenafil and were marketed without FDA approval.
Product
Pink Pussycat SENSUAL ENHANCEMENT capsule, 3000mg, 1-count blister card, Manufactured for: Pink Pussycat Products - Chatsworth, CA 91311, UPC 8 91875 00462 6.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0907-2022·2022-04-27
Philips Respironics V60 Ventilator Recalled Due to Electrical Circuit Defect
Philips Respironics V60 ventilators are recalled due to an internal electrical circuit defect that may cause the device to stop operating. Approximately 87,138 units worldwide are affected.
Product
Philips Respironics V60 Ventilator (All Models, including: 1053613, 1053614, 1053615, 1053616, 1053617, 1053618, 1076709, 1076716, 1076717, 1137292, DU1053617, U1053617, R1053618, R1076709)
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0908-2022·2022-04-27
Philips Respironics V60 Plus Ventilator Recalled for Electrical Circuit Failure Risk
Philips Respironics V60 Plus Ventilators are recalled for an internal electrical circuit defect that could cause the device to stop operating. Approximately 12,145 units were affected worldwide.
Product
Philips Respironics V60 Plus Ventilator (All Models, including: 1138747, 1137276)
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0909-2022·2022-04-27
Philips Respironics V680 Ventilator May Stop Operating Due to Electrical Fault
Philips Respironics V680 Ventilators may stop operating due to an internal electrical circuit fault. Units were distributed worldwide and across the United States.
Product
Philips Respironics V680 Ventilator (All Models, including: P/N 1103044 (850011)), *Distributed outside the United States
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0927-2022·2022-04-27
Medtronic Harmony Delivery Catheter System Recalled Over Equipment Failure Risk
Medtronic is recalling 1,483 Harmony Delivery Catheter Systems due to potential capsule bond failure during pulmonary valve replacement procedures. The FDA has classified this as a Class I recall affecting devices distributed in the US and Canada.
Product
Harmony Delivery Catheter System. Part of the Harmony Transcatheter Pulmonary Valve (TPV) Replacement Implantation System.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0946-2022·2022-04-27
Virus Counter Platform VC3100 Class II Medical Device Recall
Sartorius Corporation is recalling the Virus Counter Platform Model VC3100 (model numbers VIR-92166, VIR-92341) distributed nationwide to 82 units, classified as a Class II FDA medical device recall.
Product
Virus Counter Platform with Model Name VC3100
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0951-2022·2022-04-27
Genetic Testing Kit Recalled for Inaccurate Mutation Test Results
Qiagen Sciences' KRAS mutation testing kit can produce false positive or false negative results due to testing flags or warnings. 435 kits distributed across 16 U.S. states are affected.
Product
therascreen KRAS RGQ PCR Kit (24) Model Number(s): REF 870021 (US IVD)
Category
Medical Device
Distribution
17 states
HighFDA (Devices)·Z-0972-2022·2022-04-27
X-ray Imaging System May Fail to Cool Tube Properly
Siemens Artis zee biplane MN X-ray systems may have inadequate cooling in the X-ray tube circuit, causing automatic system shutdown during operation. Seven affected systems are distributed nationwide.
Product
Artis zee biplane MN, Model Number 10094143
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0947-2022·2022-04-27
Matrix COVID-19 Test Kits Recalled for Unauthorized Home Sample Collection
Matrix Medical Network is recalling 3,226 At-Home COVID-19 Test kits distributed across 24 U.S. states because the tests were not authorized by the FDA for home sample collection.
Product
Matrix Clinical Solution At-Home COVID-19 Test
Category
Medical Device
Distribution
25 states
HighFDA (Devices)·Z-0962-2022·2022-04-27
CT Scanner Software Error May Cause Scanning Interruptions and Unexpected Radiation
Siemens SOMATOM CT scanners with software syngo CT VA30A_SP4 may experience sporadic software errors causing scanning interruptions and potential unexpected radiation doses. 547 units affected nationwide.
Product
SIEMENS SOMATOM with software syngo CT VA30A_SP4 Models: SOMATOM go.Now 11061610 & 11061618 SOMATOM go.Up 11061620 & 11061628 SOMATOM go.All 11061630 & 11061638 SOMATOM go.Top 11061640 & 11061648 SOMATOM go.Sim 11061660 & 11061668 SOMATOM go.Open Pro 11061670…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0781-2022·2022-04-27
Sermorelin Acetate Injection Recalled Due to Sterility Assurance Issues
Sermorelin Acetate injectable (76 vials) recalled nationwide due to manufacturing deviations that compromise sterility assurance. No illnesses reported.
Product
Sermorelin Acetate 1 mg/mL (6 mL) Injection, 6 mL vials, Rx only, Farmakeio 1736 N Greenville Ave Richardson, TX 75081
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0958-2022·2022-04-27
Acumed Cannulated Screws May Lack Sufficient Strength for Bone Fixation
Acumed 4.0mm x 10mm Cannulated Screws may not have sufficient strength to hold bone fragments in place. This could result in improper bone healing, fracture, or soft tissue damage.
Product
4.0mm x 10mm Cannulated Screw, Short Thread; Part number 3005-40010
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0965-2022·2022-04-27
Cardiac Device Programmer Software May Fail to Terminate Test
St. Jude Medical's Merlin 2 programmer software can fail to stop a clinical Decrement Test and restore pacing parameters during in-clinic testing, affecting 401 devices worldwide.
Product
Merlin 2 PCS MER3700 programmer Model MER3400 software
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0988-2022·2022-04-27
Gallant DR Implantable Cardioverter Defibrillator Bluetooth Malfunction Affects Remote Monitoring
St. Jude Medical's Gallant DR implantable cardioverter defibrillator has a Bluetooth malfunction preventing remote monitoring and reducing battery life. The device enters inductive-only telemetry mode, requiring in-clinic monitoring instead.
Product
Gallant DR Implantable Cardioverter Defibrillator REF # CDDRA500Q
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0973-2022·2022-04-27
Artis zeego X-ray imaging system recalled for insufficient cooling
Siemens is recalling 183 Artis zeego X-ray imaging systems due to a cooling system defect that may prevent adequate X-ray tube cooling, triggering automatic system shutdown.
Product
Artis zeego, Model Number 10280959
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1007-2022·2022-04-27
New England Beach Pizza Recalled for Potential Metal Contamination
Beach Brand Foods is recalling New England Beach Pizza products due to potential metal contamination. The affected lots include Lot 087 with best-by date 11/09/2022, distributed in New Hampshire and Massachusetts.
Product
New England Beach Pizza 1. Extra Cheese 2. Cheese
Category
Food
Distribution
2 states
HighFDA (Drugs)·D-0774-2022·2022-04-27
Injectable Rifampin Recalled Due to Failed Quality Specifications
Mylan Pharmaceuticals is recalling injectable Rifampin vials nationwide due to failed impurities and degradation specifications discovered during stability testing.
Product
RIFAMPIN — RIFAMPIN (RIFAMPIN)
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·22V282000·2022-04-27
Commercial buses with inoperative collision system lack required warning label
Navistar is recalling certain 2022-2023 commercial buses equipped without forward radar units. The required warning label indicating the collision mitigation system is inoperative may be missing, increasing crash risk.
Product
INTERNATIONAL — INTERNATIONAL, IC BUS HV, MV, RE
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0975-2022·2022-04-27
X-ray Imaging System Coolant Deficiency May Disable Equipment Operation
The Artis Q X-ray system may fail to adequately cool the X-ray tube if coolant levels drop, causing the system to disable imaging and display error messages. 418 systems are affected nationwide.
Product
Artis Q ceiling, Model Number 10848281
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0963-2022·2022-04-27
Sight OLO Blood Analysis Device: Incorrect Reference Ranges May Display
The Sight OLO blood analysis device may display and print incorrect reference ranges in software versions 2.59.3 and earlier. This could occur when custom reference ranges were configured after device installation.
Product
The Sight OLO device is a computer vision based platform for blood analysis. The platform combines computer-vision algorithms for image processing to identify and quantify blood components (e.g., red blood cells) and their characteristics (e.g., cell volume) in an automated…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·22V279000·2022-04-27
Blue Bird Recalls 2023 Vision School Buses for Stop Arm Defect
Blue Bird is recalling 2023 Vision school buses because incorrect pins on the air stop arm may cause it to fail, increasing injury risk during boarding.
Product
BLUE BIRD — BLUE BIRD VISION SCHOOL BUS
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0952-2022·2022-04-27
Qiagen therascreen KRAS RGQ PCR Kit Recall: False Positive/Negative Results
Qiagen Sciences LLC is recalling the therascreen KRAS RGQ PCR Kit due to potential false positive or false negative results in KRAS G12C mutation detection. These inaccurate results could invalidate clinical test outcomes.
Product
therascreen KRAS RGQ PCR Kit (24) REF 874052 (Japan IVD, not released in the USA)
Category
Medical Device
Distribution
17 states
HighFDA (Devices)·Z-0978-2022·2022-04-27
Medical device X-ray imaging system recalled for cooling failure
Siemens Medical Solutions is recalling its Artis Q.zen X-ray imaging system due to a coolant circulation defect that may cause insufficient tube cooling and system shutdown.
Product
Artis Q.zen floor, Model Number 10848353
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·22V281000·2022-04-27
Daimler Recalls 2019-2021 Sprinter Vehicles for Rearview Camera Software Error
Daimler Vans USA is recalling 2019-2021 Freightliner and Mercedes-Benz Sprinter vans because a software error may prevent the rearview camera from displaying an image.
Product
FREIGHTLINER — FREIGHTLINER, MERCEDES-BENZ SPRINTER 4500, SPRINTER 1500, SPRINTER 2500, SPRINTER 3500
Category
Vehicle
Distribution
Distributed nationwide