State

Massachusetts product recalls

72,933 recalls have nationwide distribution and so reach Massachusetts. 8,209 additional recalls listed Massachusetts specifically in their distribution scope.

What the numbers show

Total: 8,209
Critical: 1,171
Severe: 2,013
Most recent: 2026-09-09

Of the 8,209 recalls naming Massachusetts we have scored against our rubric, 1,171 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,013 (25%) are Severe.

Which agencies issued them

These figures cover only the 8,209 recalls whose distribution notice names Massachusetts specifically. The 72,933 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

2726–2750 of 81142

HighFDA (Devices)·Z-1644-2026·2026-04-01
Olympus PKS cutting forceps jaws may break from defective welds
Olympus is recalling PKS Cutting Forceps because a supplier did not adequately validate the welding process, and defective welds can cause the forceps jaw to break during clinical use.
Product
Brand Name: Olympus PKS Cutting Forceps, 5mm 33cm Product Name: PKS Cutting Forceps Model/Catalog Number: 920005PK Product Description: The PKS Cutting Forceps are intended to be passed through a 5mm cannula. Coagulation is achieved using electrosurgical energy under visuali
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0402-2026·2026-04-01
Curosurf intratracheal suspension recalled over lack of sterility assurance
Chiesi USA is recalling three lots of Curosurf (poractant alfa) Intratracheal Suspension for lack of assurance of sterility.
Product
CUROSURF — CUROSURF (PORACTANT ALFA)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1611-2026·2026-04-01
Olympus endoscope air water valves no longer compatible with named reprocessors
Olympus is recalling the MAJ-1444 Endoscope Air/Water Valve because the MAJ-1443 and MAJ-1444 are no longer reprocessing compatible with the OER-Pro and OER-Elite automated endoscope reprocessors.
Product
Olympus Endoscope Air/Water Valve - MAJ-1444. Model Number: MAJ-1444.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·26V208000·2026-04-01
Volvo trucks recalled over turn signals that may not function properly
Volvo Trucks North America is recalling 340 VNL and VNR vehicles because the turn signals may not function properly, failing to comply with the federal lighting standard.
Product
VOLVO — VOLVO VNL (4), VNR (4)
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Food)·H-0590-2026·2026-04-01
Chilli Spanish Peanuts Recalled for Glass Contamination Risk
Western Mixers Produce & Nuts, Inc. is recalling Treasured Harvest brand Chilli Spanish Peanuts (25lb bags, Lot #260230) due to glass fragments found in sealed containers.
Product
Chilli Spanish Peanuts, Treasured Harvest brand, 25lb clear plastic bag container. UPC:none Item code: 2608-25
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1639-2026·2026-04-01
Olympus Everest bipolar cutting forceps jaws may break from defective welds
Olympus is recalling Everest Bipolar Cutting Forceps because a supplier did not adequately validate the welding process, and defective welds can cause the forceps jaw to break during clinical use.
Product
Brand Name: Olympus Everest Bipolar Cutting Forceps w/Cord, 5mm 33 cm Product Name: Everest Bipolar Cutting Forceps Model/Catalog Number: 3006 Product Description: The OLYMPUS Everest Bipolar Cutting Forceps are intended to be passed through a 5 mm cannula. Coagulation is achi
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0597-2026·2026-04-01
Ajinomoto Tai Pei Shrimp Fried Rice Recalled for Glass Contamination
Ajinomoto Foods North America Inc. is recalling Tai Pei Shrimp Fried Rice due to glass fragments found in the product. Glass pieces measuring 1–3 cm long and 2–4 mm wide pose a choking and injury risk.
Product
Item 81146 Ajinomoto Tai Pei Shrimp Fried Rice - Shrimp, vegetables & fried rice with oyster flavored sauce. Net wt. 48oz or 3lbs. per box. Retail box UPC 070077811465. Product packaging is flexible bags in a master case or flexible bags in cartons in a master case. There are 4
Category
Food
Distribution
43 states
HighFDA (Devices)·Z-1592-2026·2026-04-01
I.T.S. volar radius plates heat more in MRI than stated
I.T.S. GmbH is recalling Volar Radius Plates with Angular Stability because updated MRI safety testing shows higher RF-induced temperature increases than the Instructions for Use previously reflected.
Product
Volar Radius Plate with Angular Stability with the following description: Radius Plate PROlock II. Article Numbers: 21031-3, 21031-5, 21032-11, 21032-3, 21032-5, 21033-3, 21033-5, 21034-3, 21034-5, 21035-3, 21036-3.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1633-2026·2026-04-01
Straumann angled custom abutments made from wrong bar material
Straumann is recalling Custom Abutment AS Ti for Straumann RC because a material mix-up meant titanium abutments were manufactured from TAN bar material instead of Titanium Grade 4.
Product
Custom Abutment AS Ti, for Straumann RC, incl. TAN screw; Catalog Number/Art.: 010.5438;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1631-2026·2026-04-01
BiDop 3 pocket Doppler labeling includes uncleared fetal indication
Koven Technology is recalling the BiDop 3 Pocket Doppler packaged with a fetal probe because the product labeling includes a fetal indication for use that is not cleared under its 510(k).
Product
Brand Name: BiDop 3 Product Name: BiDop 3 Pocket Doppler (ES-100V3) with BT2M20S8C fetal probe Model/Catalog Number: ES-100V3 (device); BT2M20S8C (2 MHz fetal probe). Software Version: N/A Product Description: Hand-held, battery-powered ultrasonic Doppler blood-flow detector
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1645-2026·2026-04-01
BD Alaris system labeling omits required TLS version for secure Wi-Fi
CareFusion is recalling the BD Alaris System with Guardrails Suite MX because the product labeling does not indicate which TLS version must be enabled on the hospital network for secure Wi-Fi communication.
Product
BD Alaris" System with Guardrails" Suite MX with Point of Care Unit
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0401-2026·2026-04-01
Sodium iodide capsule packs recalled after failing capsule specifications
Radnostix is recalling three lots of the Gelatin Capsule Pack used with the Sodium Iodide I-131 Kit because the product failed tablet and capsule specifications.
Product
SODIUM IODIDE I-131 — SODIUM IODIDE I-131 (SODIUM IODIDE I-131)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1624-2026·2026-04-01
Philips OMNI III TEE transducer labelling updated to define useful life
Philips is recalling the OMNI III TEE Ultrasound Transducer to provide clarification and labelling that defines the useful life of ultrasound transducers in the field.
Product
Philips OMNI III TEE Ultrasound Transducer
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1627-2026·2026-04-01
Philips X3-1 ultrasound transducer labelling updated to define useful life
Philips is recalling the X3-1 Ultrasound Transducer to provide clarification and labelling that defines the useful life of ultrasound transducers in the field.
Product
Philips X3-1 Ultrasound Transducer
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1628-2026·2026-04-01
Philips X7-2 ultrasound transducer labelling updated to define useful life
Philips is recalling the X7-2 Ultrasound Transducer to provide clarification and labelling that defines the useful life of ultrasound transducers in the field.
Product
Philips X7-2 Ultrasound Transducer
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1626-2026·2026-04-01
Philips S5-2 ultrasound transducer labelling updated to define useful life
Philips is recalling one S5-2 Ultrasound Transducer to provide clarification and labelling that defines the useful life of ultrasound transducers in the field.
Product
Philips S5-2 Ultrasound Transducer
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1621-2026·2026-04-01
Philips L17-5 ultrasound transducer labelling updated to define useful life
Philips is recalling two L17-5 Ultrasound Transducers to provide clarification and labelling that defines the useful life of ultrasound transducers in the field.
Product
Philips L17-5 Ultrasound Transducer
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1618-2026·2026-04-01
Philips 3D6-2 ultrasound transducer labelling updated to define useful life
Philips is recalling the 3D6-2 Ultrasound Transducer to provide clarification and labelling that defines the useful life of ultrasound transducers in the field.
Product
Philips 3D6-2 Ultrasound Transducer
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1625-2026·2026-04-01
Philips S4-1 ultrasound transducer labelling updated to define useful life
Philips is recalling the S4-1 Ultrasound Transducer to provide clarification and labelling that defines the useful life of ultrasound transducers in the field.
Product
Philips S4-1 Ultrasound Transducer
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1623-2026·2026-04-01
Philips OMNI II TEE transducer labelling updated to define useful life
Philips is recalling two OMNI II TEE Ultrasound Transducers to provide clarification and labelling that defines the useful life of ultrasound transducers in the field.
Product
Philips OMNI II TEE Ultrasound Transducer
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1622-2026·2026-04-01
Philips Mini Multi TEE transducer labelling updated to define useful life
Philips is recalling the Mini Multi TEE Ultrasound Transducer to provide clarification and labelling that defines the useful life of ultrasound transducers in the field.
Product
Philips Mini Multi TEE Ultrasound Transducer
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1620-2026·2026-04-01
Philips L12-5 ultrasound transducer labelling updated to define useful life
Philips is recalling the L12-5 Ultrasound Transducer to provide clarification and labelling that defines the useful life of ultrasound transducers in the field.
Product
Philips L12-5 Ultrasound Transducer
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1619-2026·2026-04-01
Philips C9-4 ultrasound transducer labelling updated to define useful life
Philips is recalling one C9-4 Ultrasound Transducer to provide clarification and labelling that defines the useful life of ultrasound transducers in the field.
Product
Philips C9-4 Ultrasound Transducer
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·26V201000·2026-03-31
2025–2026 Ford Bronco Sport and Maverick Occupant Sensor Recall
Ford is recalling certain 2025–2026 Bronco Sport and Maverick vehicles because the front passenger occupant classification sensor may fail to detect a passenger, risking failure of the airbag to deploy in a crash.
Product
FORD — FORD MAVERICK, BRONCO SPORT
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·26V205000·2026-03-31
2026 Ford Explorer and Mustang Engine Piston Circlip Defect Recall
Ford is recalling certain 2026 Explorer and Mustang vehicles because engine piston circlips may have been incorrectly installed, risking loss of drive power and increasing crash risk.
Product
FORD — FORD EXPLORER, MUSTANG
Category
Vehicle
Distribution
Distributed nationwide