The Recall Desk

State

Massachusetts product recalls

73,827 recalls have nationwide distribution and so reach Massachusetts. 8,252 additional recalls listed Massachusetts specifically in their distribution scope.

What the numbers show

Total
8,252
Critical
1,179
Severe
2,360
Most recent
2026-11-04

Of the 8,252 recalls naming Massachusetts we have scored against our rubric, 1,179 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,360 (29%) are Severe.

These figures cover only the 8,252 recalls whose distribution notice names Massachusetts specifically. The 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

47451–47475 of 82079

  • HighFDA (Devices)·Z-2713-2017·2017-07-19

    Pentax Video Duodenoscope Recall for Surface Soiling Investigation

    Pentax of America Inc. issued a field correction for two Video Duodenoscope models to investigate surface soiling on the suction cylinder and distal cap.

    Product
    Video Duodenoscope These instruments are intended to provide optical visualization of (via a video monitor), and therapeutic access to, the biliary tract via the upper GI tract. This anatomy includes, but is not restricted to, the organs; tissues; and subsystems: esophagus…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2682-2017·2017-07-19

    ICU Recalls Plum A+ Infusion Systems Due to Battery Error

    ICU is recalling 7,351 Plum A+ Infusion Systems because a battery issue can trigger an E321 error code, potentially interrupting therapy.

    Product
    The Plum A+ Infusion Systems are a multipurpose family of devices that provides precise delivery of multiple therapies across the general spectrum of clinical care. The Plum A+ family infusion pumps are self contained, microprocessor based infusion devices. The pumps are…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2569-2017·2017-07-19

    National Fish & Seafood Recalls Perch Fillets for Undeclared Milk

    National Fish & Seafood, Inc. is recalling Schooner Pre-Cooked Crunchy Perch Fillets because the product may contain undeclared milk.

    Product
    SCHOONER PRE-COOKED CRUNCHY PERCH FILLETS 12/16 OZ
    Category
    Food
    Distribution
    24 states
  • HighFDA (Devices)·Z-2728-2017·2017-07-19

    Natus Neurology Recalls Elite Obstetric Probes Due to Excessive Background Noise

    Natus Neurology is recalling 2,335 Elite Obstetric probes because excessive background noise may mask heart rate and blood flow sounds.

    Product
    Nicolet¿ Elite¿ 3 MHz OB Probe, Model #: X1L001, Catalog Code: N300. Intended for non-invasive support, i.e. early detection of fetal life, monitor blood flow before and after surgery, etc.
    Category
    Medical Device
    Distribution
    44 states
  • HighFDA (Food)·F-2556-2017·2017-07-19

    Murrys Pre-Cooked Steaks Recalled for Undeclared Milk Allergen

    National Fish & Seafood, Inc. is recalling specific lots of Murrys Pre-Cooked Steaks because the product may contain undeclared milk.

    Product
    MURRYS PRE COOKED STEAKS 6/2.4 3.2 OZ, 9/4 3.2 OZ
    Category
    Food
    Distribution
    24 states
  • HighFDA (Devices)·Z-2680-2017·2017-07-19

    ICU Plum A+ Infusion Systems Recalled for Battery-Related Therapy Interruption

    ICU is recalling 7,848 Plum A+ Infusion Systems because a battery issue can trigger an E321 error code, potentially interrupting patient therapy.

    Product
    The Plum A+ Infusion Systems are a multipurpose family of devices that provides precise delivery of multiple therapies across the general spectrum of clinical care. The Plum A+ family infusion pumps are self contained, microprocessor based infusion devices. The pumps are…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2572-2017·2017-07-19

    Schooner Pre-Cooked Crunchy Whiting Fillets Recalled for Undeclared Milk

    National Fish & Seafood, Inc. is recalling Schooner Pre-Cooked Crunchy Whiting Fillets because the product may contain undeclared milk.

    Product
    SCHOONER PRE-COOKED CRUNCHY WHITING FILLETS 1/10 LB and SCHOONER PRE-COOKED CRUNCHY WHITING FILLETS 12/16 OZ
    Category
    Food
    Distribution
    24 states
  • HighFDA (Devices)·Z-2678-2017·2017-07-19

    ICU Recalls 214 Plum A+ Infusion Systems Due to Battery Error

    ICU is recalling 214 Plum A+ Infusion Systems because a battery issue can trigger an E321 error code, potentially interrupting therapy.

    Product
    The Plum A+ Infusion Systems are a multipurpose family of devices that provides precise delivery of multiple therapies across the general spectrum of clinical care. The Plum A+ family infusion pumps are self contained, microprocessor based infusion devices. The pumps are…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2548-2017·2017-07-19

    Lil Fisherman Pollock Sticks Recalled for Undeclared Milk

    National Fish & Seafood, Inc. is recalling Lil Fisherman Pre Cooked Pollock Sticks because the product may contain undeclared milk.

    Product
    LIL FISHERMAN PRE COOKED POLLOCK STICKS 1 OZ GRADE A 10 LB
    Category
    Food
    Distribution
    24 states
  • HighFDA (Devices)·Z-2691-2017·2017-07-19

    St. Jude Medical Recalls Proclaim 5 Elite Implantable Pulse Generators

    St. Jude Medical is recalling 8,780 Proclaim 5 Elite implantable pulse generators due to a risk of losing neuromodulation therapy when exposed to monopolar electrosurgical devices.

    Product
    Proclaim 5 Elite, implantable Pulse Generator, REF 3660, Rx only, STERILE EO Product Usage: The Proclaim implantable pulse generator (IPG) is an electronic device designed to be connected to one or more extensions or leads with up to 16 electrodes total. It is powered by a…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2707-2017·2017-07-19

    Merge Healthcare Recalls Schiller PB 1000 Patient Data Module

    Merge Healthcare is recalling 555 Schiller PB 1000 Patient Data Modules because the analog output may not accurately reflect the pressure waveform used for fractional flow reserve calculations.

    Product
    The Schiller PB 1000, also known as Merge Hemo Patient Data Module (PDM), a major component of the Merge Hemo software.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2726-2017·2017-07-19

    Natus Neurology Recalls Elite 2 MHz OB Probes Due to Excessive Noise

    Natus Neurology is recalling 2,335 Elite 2 MHz OB probes because excessive background noise may mask the user's ability to hear heart rate or blood flow.

    Product
    Nicolet¿ Elite¿ 2 MHz OB Probe, Non-Fetal Monitor, Model #: X1L007, Catalog Code: N200. Intended for non-invasive support, i.e. early detection of fetal life, monitor blood flow before and after surgery, etc.
    Category
    Medical Device
    Distribution
    44 states
  • HighFDA (Food)·F-2466-2017·2017-07-19

    3CS Organics Recalls Unapproved Holle Goat Milk Infant Formula

    3CS Organics LLC is recalling Holle goat milk infant formula products that are not FDA approved and lack English labeling.

    Product
    HOLLE Bio Lait Pour Nourrissons Au Lait De Chevre, Zuigelingenmelk OP Geitenmelbasis, 1, 400g (4/case), HOLLE Bio-Flogemilch Auf Ziegenmilchbasis, 1, 400g (4/case), HOLLE Bio-Folgenmilch Auf Ziegenmilchbasis, 3, 400g (4/case), HOLLE Bio-Folgemich, 2, 600g (3bx/case), HOLLE…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2546-2017·2017-07-19

    Lil Fisherman Pollock Nuggets Recalled for Undeclared Milk

    National Fish & Seafood, Inc. is recalling Lil Fisherman Pre Cooked Pollock Nuggets because they may contain undeclared milk.

    Product
    LIL FISHERMAN PRE COOKED POLLOCK NUGGETS 1 OZ PUFI 1/10 LB
    Category
    Food
    Distribution
    24 states
  • HighFDA (Food)·F-2551-2017·2017-07-19

    Matlaws Buffalo Popcorn Shrimp Recalled for Undeclared Milk

    National Fish & Seafood, Inc. is recalling Matlaws Buffalo Popcorn Shrimp because the product may contain undeclared milk.

    Product
    MATLAWS P/C BRD BUFFALO POPCORN SHRIMP 12/8 OZ
    Category
    Food
    Distribution
    24 states
  • HighFDA (Food)·F-2570-2017·2017-07-19

    Schooner Pre-Cooked Cod Fillets Recalled for Undeclared Milk

    National Fish & Seafood, Inc. is recalling Schooner Pre-Cooked Crunchy Styled Cod Fillets because the product may contain undeclared milk.

    Product
    SCHOONER PRE-COOKED CRUNCHY STYLED COD FILLET 10 LB and SCHOONER PRE-COOKED CRUNCHY STYLED COD FILLETS 12/16 OZ
    Category
    Food
    Distribution
    24 states