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.

Which agencies issued them

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.

48126–48150 of 82079

HighFDA (Devices)·Z-2263-2017·2017-06-14
Arrow Central Venous Catheter Kit Recalled for Needlestick Injury Risk
Arrow International is recalling 43,394 units of ARROWg+ard Blue PLUS Two-Lumen Central Venous Catheterization Kits due to safety cover disengagement and needlestick injury reports.
Product
ARROWg+ard Blue PLUS(R) Two-Lumen Central Venous Catheterization Kit. The Arrow(r) CVC is indicated to provide short-term (<30 days) central venous access for treatment of diseases or conditions requiring central venous access including, but not limited to: multiple infusions…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-2293-2017·2017-06-14
Pinnacle Foods Recalls Aunt Jemima Mini Pancakes Due to Listeria Risk
Pinnacle Foods is recalling Aunt Jemima Lil' Griddles Mini pancakes nationwide due to a potential for Listeria monocytogenes contamination.
Product
AUNT JEMIMA(R) LIL' GRiDDLES(TM) MINI pancakes, 40 COUNT, NET WT 14.5oz UPC 019600054801
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-2303-2017·2017-06-14
Pinnacle Foods Recalls Aunt Jemima Waffles Due to Listeria Risk
Pinnacle Foods is recalling Aunt Jemima Homestyle Waffles nationwide due to a potential for Listeria monocytogenes contamination.
Product
AUNT JEMIMA(R) 14 HOMESTYLE WAFFLES, NET WT 17.18oz UPC 019600062004
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-2305-2017·2017-06-14
Aunt Jemima Blueberry Waffles Recalled for Listeria Risk
Pinnacle Foods is recalling Aunt Jemima 14 Blueberry Waffles due to potential Listeria monocytogenes contamination. The recall covers 153,513 units distributed nationwide.
Product
AUNT JEMIMA(R) 14 BLUEBERRY WAFFLES, NET WT 17.18oz UPC 019600062202
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-2309-2017·2017-06-14
Aunt Jemima Mini Cinnamon Roll Pancakes Recalled for Listeria Risk
Pinnacle Foods is recalling Aunt Jemima Mini Cinnamon Roll Pancakes due to a potential for Listeria monocytogenes contamination.
Product
AUNT JEMIMA(R) MiNi pancakes, CINNAMON ROLL, NET WT 3.2 OZ, UPC 001960043568
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0892-2017·2017-06-14
Qualgen Recalls Estradiol Pellets Due to Quality Assurance Deviations
Qualgen is recalling Estradiol 18 mg pellets due to CGMP deviations and lack of quality assurance. The recall covers 6,361 pellets distributed nationwide.
Product
Estradiol 18 mg pellet , 99.5% Estradiol USP, .5% Stearic Acid NF in 1 count, 12 count, and 30 count bottles, Sterile Office Use Only, Subcutaneous Use Only, Rx Only, Manufactured by: Qualgen 14844 Bristol Park Blvd Edmond, OK 73013 NDC: 69761-018-01.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0881-2017·2017-06-14
Spectrum Laboratory Estradiol API Recalled for CGMP Deviations
Spectrum Laboratory Products is recalling Estradiol active pharmaceutical ingredient due to Good Manufacturing Practice deviations found during an FDA inspection.
Product
Estradiol (17-B-Estradiol; Estra-1,3,5(10)-triene-3, 17B-diol; Oestradiol) Plant Base, Micronized, U.S.P active pharmaceutical ingredient, packaged in 1g, 5g, 25g, 6 x 25g, and 100g containers, Rx only, Spectrum Chemical Mfg. Corp, Gardena, CA 90248, New Brunswick, NJ 08901…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0885-2017·2017-06-14
Dr. Reddy's Recalls Zenatane Isotretinoin Capsules for Dissolution Failures
Dr. Reddy's Laboratories is recalling Zenatane (isotretinoin) capsules because some lots failed to meet dissolution specifications, potentially affecting drug absorption.
Product
ZENATANE — ZENATANE (ISOTRETINOIN)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2314-2017·2017-06-14
Cook Medical Recalls LapSac Introducers Due to Inadequate Reprocessing Instructions
Cook Medical is voluntarily recalling LapSac Introducers because the reprocessing instructions do not provide sufficient detailed information for cleaning, disinfection, and sterilization.
Product
LapSac Introducer, Supplied sterilized by ethylene oxide gas in peel-open packages. Used to aid in the introduction of a LapSac during endoscopic surgical procedures.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0887-2017·2017-06-14
Perrigo Recalls Option 2 Emergency Contraceptive Tablets Due to Missing Blister
L. Perrigo Company is recalling Option 2 emergency contraceptive tablets because some cartons are missing the tablet blister strip and tablet.
Product
OPTION 2 — OPTION 2 (LEVONORGESTREL)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0883-2017·2017-06-14
Dr. Reddy's Recalls Zenatane Isotretinoin Capsules for Dissolution Failures
Dr. Reddy's Laboratories is recalling Zenatane (isotretinoin) capsules because some lots failed to meet dissolution specifications, potentially affecting drug absorption.
Product
ZENATANE — ZENATANE (ISOTRETINOIN)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2313-2017·2017-06-14
Cook Medical Recalls Endoscopic Curved Needles Due to Reprocessing Instruction Deficiencies
Cook Medical is voluntarily recalling 725 units of endoscopic curved needles because the reprocessing instructions do not provide sufficient detail for proper cleaning and sterilization.
Product
Endoscopic Curved Needle, Surgical Needle Guide, Supplied sterilized by ethylene oxide gas in peel-open packages. Used for internal suturing under direct vision during intraabdominal endoscopic procedures. The needle driver design affords precise placement and control of…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2307-2017·2017-06-14
Arrow International Recalls Hemodialysis Catheterization Kits
Arrow International Inc is recalling specific hemodialysis catheterization kits due to a lack of clinical data supporting the antimicrobial surface's effectiveness in preventing infections.
Product
ARROWg+ard Blue You-Bend Two-Lumen Hemodialysis Catheterization Kit for High Volume Infusions The Arrow(r) CVC is indicated to provide short-term ( < 30 days) central venous access for treatment of diseases or conditions requiring central venous access including, but not…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2310-2017·2017-06-14
Cook Medical Recalls Willscher Vas Reapproximator Sets Due to Reprocessing Instructions
Cook Medical is voluntarily recalling Willscher Vas Reapproximator Sets because the reprocessing instructions lack sufficient detail for proper cleaning, disinfection, and sterilization.
Product
Willscher Vas Reapproximator Set, Surgical Instrument, Supplied sterilized by ethylene oxide gas in peel-open packages. Used to stabilize the vas ends during microscopic vasovasostomy.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2220-2017·2017-06-14
Iba Dosimetry Recalls Large Stealth Chamber Dosimeters for Measurement Deviations
Iba Dosimetry is recalling 110 Large Stealth Chambers because they may show measurement deviations and geometric shadowing when used as reference detectors.
Product
Large Stealth Chamber, Catalog Numbers: DS50-001-XL-T, DS50-002-XL-T, DS50-003-XL-T, DS50-102-XL-T, DS50-103-XL-T
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2311-2017·2017-06-14
Cook Medical Recalls Willscher Vas Skewers Due to Insufficient Reprocessing Instructions
Cook Medical is voluntarily recalling Willscher Vas Skewers because the provided instructions do not contain sufficient detail for proper cleaning, disinfection, and sterilization.
Product
Willscher Vas Skewers, Surgical Instrument, Supplied sterilized by ethylene oxide gas in peel-open packages. Used to stabilize the vas ends during microscopic vasovasostomy.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0889-2017·2017-06-14
Qualgen Recalls Estradiol Pellets Due to Quality Assurance Deviations
Qualgen is recalling Estradiol 25 mg pellets due to CGMP deviations and lack of quality assurance. The recall covers 1,153 pellets distributed nationwide.
Product
Estradiol 25 mg pellet 99.5% Estradiol USP, .5% Stearic Acid NF, in 1 count, 12 count, and 30 count bottles, Sterile Office Use Only, For Subcutaneous Use Only. Rx Only ,Manufactured by: Qualgen 14844 Bristol Park Blvd Edmond, OK 73013 NDC 69761-025-01,
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0896-2017·2017-06-14
Qualgen Estradiol Pellets Recalled for Quality Assurance Deviations
Qualgen is recalling Estradiol 6 mg pellets due to CGMP deviations and lack of quality assurance. The recall covers 4,815 pellets distributed nationwide.
Product
Estradiol 6 mg pellet 99.5% Estradiol USP, .5% Stearic Acid NF in 1 count, 12 count, and 30 count bottles, Sterile Office Use Only, For Subcutaneous Use Only Rx Only, Manufactured by; Qualgen 14844 Bristol Park Blvd. Edmond, OK 73013 NDC: 69761-006-01.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0893-2017·2017-06-14
Qualgen Recalls Estradiol Pellets Due to Quality Assurance Deviations
Qualgen is recalling Estradiol 15 mg pellets due to CGMP deviations and lack of quality assurance. The recall covers 6,227 units distributed nationwide.
Product
Estradiol 15 mg pellet 99.5% Estradiol USP, .5% Stearic Acid NF in 1 count, 12 count, and 30 count bottles. Sterile Office Use Only, For Subcutaneous Use Only, Rx Only, Manufactured by: Qualgen 14844 Bristol Park Blvd Edmond, OK 73013, NDC: 69761-015-01
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0884-2017·2017-06-14
Dr. Reddy's Recalls Zenatane Isotretinoin Capsules for Dissolution Failure
Dr. Reddy's is recalling Zenatane (isotretinoin) capsules because some lots failed to meet dissolution specifications, potentially affecting drug absorption.
Product
ZENATANE — ZENATANE (ISOTRETINOIN)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0886-2017·2017-06-14
Dr. Reddy's Recalls Zenatane Capsules for Low Dissolution
Dr. Reddy's Laboratories is recalling Zenatane (isotretinoin) capsules because some lots failed to meet dissolution specifications.
Product
ZENATANE — ZENATANE (ISOTRETINOIN)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2315-2017·2017-06-14
Cook Medical Recalls LapSac Introducer Sets Due to Insufficient Reprocessing Instructions
Cook Medical is voluntarily recalling 335 LapSac Introducer Sets because the provided reprocessing instructions lack sufficient detail for proper cleaning, disinfection, and sterilization.
Product
LapSac Introducer Set, Bag, Extraction, Supplied sterilized by ethylene oxide gas in peel-open packages. Used to aid in the introduction of a LapSac during endoscopic surgical procedures.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2312-2017·2017-06-14
Cook Medical Recalls Willscher Vas Reapproximator Plates Due to Reprocessing Instructions
Cook Medical is voluntarily recalling Willscher Vas Reapproximator Plates because the reprocessing instructions lack sufficient detail for cleaning, disinfection, and sterilization.
Product
Willscher Vas Reapproximator Plate, Surgical Instrument, Supplied sterilized by ethylene oxide gas in peel-open packages. Used to stabilize the vas ends during microscopic vasovasostomy.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0895-2017·2017-06-14
Qualgen Recalls Estradiol Pellets Due to Quality Assurance Deviations
Qualgen is recalling Estradiol 10 mg pellets due to CGMP deviations and lack of quality assurance. The recall covers 5,260 pellets distributed nationwide.
Product
Estradiol 10 mg pellet 99.5% Estradiol USP, .5% Stearic Acid NF in 1 count, 12 count, and 30 count bottles, Sterile Office Use Only , For Subcutaneous Use Only Rx Only Manufactured by: Qualgen 14844 Bristol Park Blvd Edmond, OK 73013 NDC: 69761-010-01
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0891-2017·2017-06-14
Qualgen Recalls Estradiol Pellets Due to Quality Assurance Deviations
Qualgen is recalling Estradiol 20 mg pellets due to CGMP deviations and lack of quality assurance. The recall covers 4,468 pellets distributed nationwide.
Product
Estradiol 20 mg pellet 99.5% Estradiol USP, .5% Stearic Acid NF in 1 count and 12 count bottles, Sterile Office Use Only, For Subcutaneous Use Only Rx Only, Manufactured by Qualgen 14844 Bristol Park Blvd Edmond, OK 73013 NDC: 69761-020-01
Category
Drug
Distribution
Distributed nationwide