State

Massachusetts product recalls

73,503 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 73,503 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

22751–22775 of 81744

HighFDA (Food)·F-1096-2022·2022-06-08
Potato & American Cheese Pierogi Recalled for Undeclared Milk
Dymski Pierogi LLC is recalling Potato & American Cheese Pierogi products because they contain undeclared milk. The recall affects products distributed in New Jersey, Massachusetts, and Pennsylvania.
Product
Potato & American Cheese Pierogi Grandma s Cuisine Potato & American Cheese Pierogi UPC: 8 67355 00032 7 16oz (454g) / 1 dozen Golden Eagle Potato & American Cheese Pierogis UPC: 7 05105 70400 5 16 oz
Category
Food
Distribution
3 states
HighFDA (Drugs)·D-0957-2022·2022-06-08
Hydromorphone Injection Recalled Due to Lack of Sterility Assurance
Nephron Sterile Compounding Center is recalling Hydromorphone HCl Injection 50 mg/50 mL pre-filled syringes due to lack of sterility assurance. The recalled product was distributed nationwide.
Product
Hydromorphone HCl Injection, USP, 50 mg/50 mL (1 mg/mL), 50 mL Pre-Filled Syringe, 5 x 50 mL Pre-Filled Syringes, 6 x 5 Syringe Carton, Rx Only, Nephron 503B outsourcing facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC: 69374-559-50
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0959-2022·2022-06-08
Ketamine Hydrochloride Injectable Recalled Due to Sterility Assurance Issues
Nephron Sterile Compounding Center LLC is recalling 30,290 syringes of Ketamine Hydrochloride Injection due to lack of assurance of sterility. The injectable drug was distributed nationwide.
Product
Ketamine Hydrochloride Injection, USP, 30 mg/3 mL (10 mg/mL), 3 mL Pre-Filled Syringe, 5 x 3 mL Pre-Filled Syringes, 6 x 5 Syringe Carton, Rx Only, Nephron 503B outsourcing facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC: 69374-982-33
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1225-2022·2022-06-08
Hip Stem Prosthetic Missing Plasma Coating in Manufacturing Lot
MicroPort Orthopedics is recalling one manufacturing lot of PROFEMUR PLASMA Z CLASSIC hip stem prosthetics due to missing plasma-spray coating in the proximal region of the implant stem.
Product
PROFEMUR PLASMA Z CLASSIC STEM SIZE 7 STANDARD SHORT NECK
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1097-2022·2022-06-08
Dymski Pierogi Recalls Sweet Cheese Pierogi for Undeclared Milk and Wheat
Dymski Pierogi LLC is recalling Sweet Cheese Pierogi products with undeclared milk and wheat allergens. Approximately 1,721 units were distributed to retail and food service locations in NJ, MA, and PA.
Product
Sweet Cheese Pierogi Grandma s Cuisine Sweet Cheese Pierogi 0 67355 00034 5 16oz (454g) / 1 dozen Bernat s Sweet Cheese 16oz (450g) Golden Eagle Sweet Cheese Pierogis 14 oz
Category
Food
Distribution
3 states
HighFDA (Drugs)·D-0964-2022·2022-06-08
Oxytocin Injectable Drug Recalled for Lack of Sterility
Nephron Sterile Compounding Center has recalled 3,587 bags of Oxytocin injectable nationwide due to lack of assurance of sterility.
Product
Oxytocin 30 Units/500 mL (0.06 Units/mL) in 0.9% Sodium Chloride Injection, USP, 500 mL Single-Dose Container Bag, 10 x 1 IV Bag, Rx Only Nephron 503B outsourcing facility 4500 12th St. Extension West Columbia, SC 29172 NDC: 69374-543-50
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0958-2022·2022-06-08
Injectable Hydromorphone Recalled for Lack of Sterility Assurance
Nephron Sterile Compounding Center is recalling Hydromorphone HCl Injection due to lack of assurance of sterility. The recall affects 6,210 pre-filled syringes distributed nationwide.
Product
Hydromorphone HCl Injection, USP, 6 mg/30 mL (0.2 mg/mL), 30 mL Pre-Filled Syringe, 5 x 30 mL Pre-Filled Syringes, 6 x 5 Syringe Carton, Rx Only, Nephron 503B outsourcing facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC: 69374-529-30
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0963-2022·2022-06-08
Neostigmine Methylsulfate Injection Recalled Due to Sterility Assurance Failure
Nephron Sterile Compounding Center is recalling Neostigmine Methylsulfate Injection due to lack of assurance of sterility. The compounded injectable drug may not meet sterile product standards.
Product
Neostigmine Methylsulfate Injection, USP, 5 mg/5 mL (1 mg/mL), Preservative Free, 5 mL Pre-Filled Syringe, 5 x 5 mL Pre-Filled Syringes, 6 x 5 Syringe Carton, Rx Only Nephron 503B outsourcing facility 4500 12th St. Extension West Columbia, SC 29172 NDC: 69374-902-05
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0976-2022·2022-06-08
AMBI Skincare Fade Cream Recalled for Temperature Storage Deviations
AMBI Skincare Fade Cream is being recalled nationwide due to cGMP violations. The product was stored outside its labeled temperature requirements during manufacturing.
Product
AMBI Skincare Fade Cream Normal Skin, Net Wt. 2 OZ. (56g)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1147-2022·2022-06-08
I.V. Start Kit with Swab Products Recalled for Manufacturing Validation Issues
Busse Hospital Disposables is recalling I.V. Start Kits containing swab products due to inadequate validation of manufacturing test methods. Approximately 2,475 units nationwide may be affected.
Product
I.V. Start Kit - Tegaderm Dressing - Catheter Securement - Prevantics Catalog Number: 822
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1213-2022·2022-06-08
Abbott FIRMap Catheter Recalled for Incorrect Product Labeling
Abbott is recalling 40 units of FIRMap® Catheter, 60mm Basket due to incorrect product labeling. The recall affects devices distributed in Missouri, California, Ohio, Washington and internationally in Italy and Netherlands.
Product
FIRMap" Catheter, 60mm Basket
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1180-2022·2022-06-08
Swab and Swabstick Drug Products Recalled Due to Validation Uncertainty
Busse Convenience kits with swab and swabstick drug products are being recalled because the validation of the test methods used during manufacturing is uncertain.
Product
"3.2MM Pellet Insertion Tray with Medium Gloves" Catalog Number: B1351
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1142-2022·2022-06-08
Locking Cap for PD Catheter Adapter Distributed Without FDA Clearance
Baxter Healthcare is recalling locking caps for peritoneal dialysis catheters that were distributed without FDA regulatory clearance. These devices were released into the U.S. market in error.
Product
Locking Cap for PD Catheter Adapter
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1193-2022·2022-06-08
Busse Convenience Kit Swab Products Recalled for Test Method Validation Issues
Busse Convenience kits containing swab and swabstick drug products manufactured by Professional Disposables International are being recalled due to uncertainty about test method validation during manufacturing.
Product
SS 4.5MM DIAMOND TIP TROCAR WITH MEDIUM GLOVES Catalog Number: B1560
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1195-2022·2022-06-08
Convenience Kits with Drug Swab Products Recalled for Validation Uncertainty
Busse Convenience kits containing swab/swabstick drug products are being recalled nationwide due to uncertainty about the adequacy of the validation of manufacturing test methods.
Product
Male SS 4.5MM Pellet Insertion Tray Catalog Number: B1570
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1184-2022·2022-06-08
Pellet Insertion Tray Recall for Uncertain Manufacturing Test Validation
Busse Hospital Disposables is recalling SS 3.5MM Pellet Insertion Tray kits nationwide. The kits contain swab products with uncertain manufacturing test method validation.
Product
SS 3.5MM Pellet Insertion Tray with Medium Gloves Catalog Number: B1354R1
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1144-2022·2022-06-08
Baxter Effluent Sample Bags Recalled for Lack of FDA Clearance
Baxter Healthcare recalled 78 Effluent Sample Bags that were distributed without FDA regulatory clearance. The product was distributed in error across eight states.
Product
Effluent Sample Bag
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1214-2022·2022-06-08
BD Anti-Kappa Flow Cytometry Reagents Recalled for Uncharacteristic Flow Profiles
BD Anti-Kappa APC and PE reagents used in flow cytometry testing may exhibit uncharacteristic flow profiles, potentially affecting test accuracy. Worldwide distribution to 249 units across US states and Taiwan.
Product
BD Anti-Kappa APC (Cat. No. 341098) is an analyte specific reagent for the Anti-Kappa antibody, which specifically recognizes the kappa light chains of human immunoglobulins. Anti-Kappa is used for in vitro identification of cells expressing the kappa light chains using flow…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1156-2022·2022-06-08
Medical Swabs Recalled Due to Manufacturing Test Method Validation Uncertainty
Busse Convenience kits containing medical swabs and sticks have been recalled due to uncertainty about whether the manufacturing test methods used were adequately validated.
Product
Port Tray Catalog 7607
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1192-2022·2022-06-08
Busse Hospital Disposables Convenience Kit Swab Recall for Test Validation Uncertainty
Busse Hospital Disposables is recalling convenience kits containing swab products due to uncertainty about adequate validation of manufacturing test methods.
Product
SS 4.5MM DIAMOND TIP TROCAR WITH LARGE GLOVES Catalog Number:B1559
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0981-2022·2022-06-08
Aveeno Daily Moisturizing Lotion recalled due to improper storage conditions
Family Dollar and Johnson & Johnson Consumer are recalling Aveeno Daily Moisturizing Lotion due to cGMP violations involving improper storage temperature. No illnesses have been reported.
Product
Aveeno Daily Moisturizing lotion Fragrance Free with Soothing Oat & Rich Emollients, Net Wt. 5 oz (141 g), Distributed by Johnson & Johnson Consumer, Inc. Skillman, NJ 08558, UPC 3 81137-001530 7
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1178-2022·2022-06-08
Procedural Accessory Kit Recalled for Manufacturing Validation Uncertainty
Busse Hospital Disposables is recalling Procedural Accessory Kits containing swabs due to uncertainty regarding the validation of manufacturing test methods. No illnesses or injuries have been reported.
Product
Procedural Accessory Kit Catalog Number: 9665R2
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0980-2022·2022-06-08
Hand Sanitizer Recall: Storage Temperature Non-Compliance at Family Dollar
Family Dollar Stores is recalling Luxury Hygiene Hand Sanitizer Moisturizing Formula due to cGMP deviations related to improper storage outside labeled temperature requirements.
Product
Luxury Hygiene Hand Sanitizer Moisturizing Formula with Vitamin E, 8 FL. OZ. (236 mL), TSM Brands LLC 540 Equinox Ln Manalapan, NJ 07726, UPC 6 86275 96536 9
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1161-2022·2022-06-08
Universal Nerve Block Tray swab products recalled for manufacturing test validation concerns
Busse Hospital Disposables is recalling Universal Nerve Block Tray units (catalog 9779) due to uncertainty regarding test method validation in manufacturing the included swab/swabstick drug products. No illnesses or injuries have been reported.
Product
Universal Nerve Block Tray Catalog Number: 9779
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1190-2022·2022-06-08
FDA Recalls Swab Products for Manufacturing Validation Uncertainty
Busse Convenience kits containing swab/swabstick products from Professional Disposables International have been recalled by the FDA due to uncertainty about adequate validation of manufacturing test methods.
Product
SS 3.5MM Diamond Tip Trocar - Large Gloves Catalog Number: B1547
Category
Medical Device
Distribution
Distributed nationwide