State

Massachusetts product recalls

73,833 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.

Which agencies issued them

These figures cover only the 8,252 recalls whose distribution notice names Massachusetts specifically. The 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

51901–51925 of 82085

HighFDA (Devices)·Z-0056-2017·2016-10-19
Natus Medical Recalls Medix NatalCare LX Incubators Due to Wheel Defect
Natus Medical is recalling 104 Medix NatalCare LX Intensive Care Incubators because a defective base weld may cause wheels to bend out of alignment.
Product
The Medix NatalCare LX Intensive Care Incubator. Neonatal incubator. Item numbers: DMNCLX1; KITNC-STLX0003; KITNC-STLX0006; and KITNC-STLX0007.
Category
Medical Device
Distribution
15 states
HighFDA (Food)·F-0062-2017·2016-10-19
Gold Standard Baking Recalls Cheese Danish for Metal Shavings
Gold Standard Baking is recalling The Bakery Cheese Danish sold at Walmart due to the presence of small metal shavings.
Product
The Bakery Cheese Danish | Net Wt 14 OZ (397g) | Distributed By WAL-MART Stores, Inc, Bentonville, AR 72716 | UPC: 605388124487
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0078-2017·2016-10-19
TheraSphere Y-90 Microspheres Recalled for Incorrect Radioactivity Labeling
Biocompatibles U.K., Ltd. is recalling one dose of TheraSphere Y-90 Glass Microspheres shipped to Hong Kong because the labeled radioactivity was incorrect.
Product
TheraSphere(R) YTTRIUM-90 CLASS MICROSPHERE INJECTION TheraSphere¿ is indicated for radiation treatment or as a neoadjuvant to surgery or transplantation in patients with unresectable HCC who can have placement of appropriately positioned hepatic arterial catheters.
Category
Medical Device
Distribution
17 states
HighFDA (Food)·F-0060-2017·2016-10-19
Archer Farms Cheese Danish Recalled for Metal Shavings
Gold Standard Baking is recalling Archer Farms Cheese Danish due to the presence of small metal shavings.
Product
Archer Farms Cheese Danish | NET WT 14 OZ (397g) | Distributed by Target Corporation Minneapolis, MN 55403 | UPC 085239101094
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0059-2017·2016-10-19
Kroger Raspberry Danish Strips Recalled for Metal Shavings
Gold Standard Baking is recalling Kroger Raspberry Danish Strips due to the presence of small metal shavings.
Product
Kroger Raspberry Danish Strip, Naturally and Artificially Flavored | NET WT 14 OZ (396g) | Distributed by The Kroger Co., Cincinnati, Ohio 45202 | UPC: 011110836489
Category
Food
Distribution
Distributed nationwide
HighNHTSA·16V756000·2016-10-19
Newmar Recalls 2017 King Aire Motorhomes Due to Radar Mounting Defect
Newmar is recalling 2017 King Aire motorhomes because the collision mitigation radar may be mounted upside down, potentially decreasing performance and increasing crash risk.
Product
NEWMAR — NEWMAR KING AIRE
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Food)·F-0065-2017·2016-10-19
Gold Standard Baking Recalls Apple Crumb Coffee Cake Due to Metal Shavings
Gold Standard Baking is recalling The Bakery Apple Crumb Coffee Cake because it may contain small metal shavings.
Product
The Bakery Apple Crumb Coffee Cake| Net Wt 15 OZ (425g) | Distributed By WAL-MART Stores, Inc, Bentonville, AR 72716 | UPC: 078742052953
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0048-2017·2016-10-19
Pharmedium Heparin Syringes Recalled Due to Potential Loss of Potency
Pharmedium Services, LLC is recalling 240 Heparin Sodium syringes because stability data does not support the expiry date, posing a risk of reduced drug potency.
Product
HEPARIN Sodium Inj., USP, 5,000 USP Heparin Units per 5 mL Total Volume in a syringe, NOT FOR LOCK FLUSH, 1,000 USP Heparin Units per mL, Rx only, PharMEDium, Product code 2K1925.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0071-2017·2016-10-19
Pharmedium Recalls Methadone Syringes Due to Potential Loss of Potency
Pharmedium Services, LLC is recalling 200 syringes of methadone HCl because stability data does not support the expiration dates, posing a risk of reduced drug potency.
Product
methadone HCl, 2.5 mg per 0.5 mL, in 0.9% Sodium Chloride, 0.5 mL Total Volume in a syringe, For IV Use Only, Rx only, PharMEDium, Product code 2T6134.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0084-2017·2016-10-19
Pharmedium Recalls Neostigmine Methylsulfate Syringes Due to Stability Data Concerns
Pharmedium Services, LLC is recalling 700 syringes of neostigmine methylsulfate because stability data does not support the expiration dates, posing a risk of reduced potency.
Product
neostigmine Methylsulfate, 1 mg per mL, 3 mg per 3 mL, 3 mL Total Volume in a syringe, For IV Use, Rx only, PharMEDium, Product code 2R3551.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0047-2017·2016-10-19
Pharmedium Recalls Heparin Sodium Injections Due to Stability Data Concerns
Pharmedium Services, LLC is recalling 399 syringes of Heparin Sodium Injection because stability data does not support the expiration dates, posing a risk of loss of potency.
Product
HEPARIN Sodium Inj. USP, 15,000 USP Heparin Units per 3 mL Injection 3 mL Total Volume in a syringe, Rx only, PharMEDium, Product code 2K1210.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0031-2017·2016-10-19
Pharmedium Recalls ePHEDrine Sulfate Syringes Due to Stability Data Concerns
Pharmedium Services, LLC is recalling 1,545 syringes of ePHEDrine Sulfate because stability data does not support the expiration dates, posing a risk of reduced potency.
Product
ePHEDrine Sulfate, 10 mg per mL, in 0.9% Sodium Chloride, Preservative Free, 1 mL Total Volume in a syringe, For IV Use, Rx only, PharMEDium, Product code 2R3347.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0083-2017·2016-10-19
Zimmer Biomet Recalls Phoenix Recon Soft Tissue Sleeve Guide Instruments
Zimmer Biomet is recalling 31 Phoenix Recon Soft Tissue Sleeve Guides due to incompatibility with new revision targeting arms, which may cause surgical delays.
Product
Phoenix Recon Soft Tissue Sleeve Guide, Surgical, Instrument for the sleeve and Orthopedic Manual Surgical Instruments for the Arm Product Usage: The Phoenix Femoral Nail System is to be implanted into the femur for alignment, stabilization and fixation of fractures caused…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0079-2017·2016-10-19
Pharmedium Recalls Morphine Sulfate Syringes Due to Stability Data Concerns
Pharmedium Services, LLC is recalling 21,506 syringes of morphine sulfate because stability data does not support the expiry dates, posing a risk of potency loss.
Product
morphine Sulfate, 1 mg per mL (2 mg per 2 mL), in 0.9% Sodium Chloride, Preservative Free (Contains Sulfites), 2 mL Total Volume in a syringe, For IV use, Rx only, PharMEDium, Product code 2R3259.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0053-2017·2016-10-19
Pharmedium Recalls Ketamine Syringes Due to Potential Loss of Potency
Pharmedium Services, LLC is recalling 25 syringes of ketamine HCl because stability data does not support the expiry date, posing a risk of reduced drug potency.
Product
ketamine HCl, 10 mg per mL, 50 mg per 5 mL, in 0.9% Sodium Chloride, 5 mL Total Volume in a syringe, For IV Use, Rx only, PharMEDium, Product code 2R3234.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0033-2017·2016-10-19
Fentanyl Citrate Injection Recalled Due to Potential Loss of Potency
Pharmedium Services is recalling fentanyl citrate injection syringes because stability data does not support the expiration date, posing a risk of reduced drug potency.
Product
fentaNYL Citrate Injection, 50 mcg per mL, Preservative Free, 1 mL Total Volume in a syringe, For IV Use, Product code 2R3118, NDC 61553-118-40
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0060-2017·2016-10-19
Pharmedium Recalls Lidocaine HCl Syringes Due to Stability Data Concerns
Pharmedium Services, LLC is recalling 2,961 syringes of lidocaine HCl 1% because stability data does not support the expiration dates, posing a risk of reduced potency.
Product
lidocaine HCl, 1%, 10 mg per 1 mL, 1 mL Total Volume in a syringe, Rx only, PharMEDium, Product code 2R3102.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0061-2017·2016-10-19
Pharmedium Recalls Lidocaine HCl Syringes Due to Stability Data Concerns
Pharmedium Services, LLC is recalling 500 syringes of lidocaine HCl 1% because stability data does not support the expiry date, posing a risk of loss of potency.
Product
lidocaine HCl, 1%, 30 mg per 3 mL, 3 mL Total Volume in a syringe, Rx only, PharMEDium, Product code 2R3104.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0027-2017·2016-10-19
Pharmedium Recalls Buffered Lidocaine Syringes Due to Stability Data Concerns
Pharmedium Services, LLC is recalling 660 syringes of Buffered Lidocaine because stability data does not support the expiry dates, posing a risk of potency loss.
Product
Buffered Lidocaine, 1%, In Sodium Bicarbonate 8.4%, 1 mL Total Volume in a syringe, Local anesthetic use, Rx only, PharMEDium, Product code 2K2466.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0084-2017·2016-10-19
Zimmer Biomet Recalls Phoenix Recon Targeting Arm Surgical Instruments
Zimmer Biomet is recalling 31 Phoenix Recon Targeting Arm surgical instruments because old and new revisions are not interchangeable, potentially causing surgical delays.
Product
Phoenix Recon Targeting Arm Guide, Surgical, Instrument for the sleeve and Orthopedic Manual Surgical Instruments for the Arm Product Usage: The Phoenix Femoral Nail System is to be implanted into the femur for alignment, stabilization and fixation of fractures caused by…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0089-2017·2016-10-19
Pharmedium Recalls Rocuronium Bromide Syringes Due to Stability Data Concerns
Pharmedium Services, LLC is recalling 6,970 syringes of rocuronium bromide because stability data does not support the expiration dates, posing a risk of reduced drug potency.
Product
rocuronium Bromide, 10 mg per mL, 50 mg per 5 mL, Preservative Free, 5 mL Total Volume in a syringe, For IV Use, Rx only, PharMEDium, Product code 2R3321.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0058-2017·2016-10-19
Pharmedium Recalls Labetalol HCl Syringes Due to Stability Data Concerns
Pharmedium Services, LLC is recalling 969 syringes of labetalol HCl because stability data does not support the expiry dates, posing a risk of loss of potency.
Product
labetalol HCl, 5 mg per mL, 20 mg per 4 mL, 4 mL total Volume in a syringe, For IV Use, Rx only, PharMEDium, Product code 2R3117.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0064-2017·2016-10-19
Pharmedium Recalls Lidocaine HCl Syringes Due to Stability Data Concerns
Pharmedium Services, LLC is recalling 300 syringes of lidocaine HCl 1% because stability data does not support the expiry date, posing a potential loss of potency.
Product
lidocaine HCl 1%, 10 mg per mL (50 mg per 5 mL), Preservative Free, 5 mL Total Volume in a syringe, Rx only, PharMEDium, Product code 2R3391.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0050-2017·2016-10-19
Pharmedium Recalls Hydromorphone Syringes Due to Stability Data Concerns
Pharmedium Services, LLC is recalling 1,916 syringes of Hydromorphone HCl because stability data does not support the expiration dates, posing a risk of reduced potency.
Product
HYDROmorphone HCl, 0.2 mg per mL, (0.4 mg per 2 mL), in 0.9% Sodium Chloride, 2 mL Total Volume in a syringe, For IV Use, Rx only, PharMEDium, Product code 2R3162.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0041-2017·2016-10-19
Pharmedium Recalls Fentanyl Citrate Syringes Due to Stability Data Concerns
Pharmedium Services, LLC is recalling 616 syringes of fentanyl citrate because stability data does not support the expiry dates, posing a risk of loss of potency.
Product
fentaNYL Citrate, 10 mcg per mL (25 mcg per 2.5 mL), in 0.9% Sodium Chloride, 2.5 mL Total Volume in a syringe, For IV Use, Rx only, PharMEDium, Product code 2R3424.
Category
Drug
Distribution
Distributed nationwide