State
73,478 recalls have nationwide distribution and so reach Massachusetts. 8,241 additional recalls listed Massachusetts specifically in their distribution scope.
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 73,478 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
SOCO Creamery ice cream base mix is being recalled due to potential Listeria monocytogenes contamination. Affected consumers in Vermont, Maine, and Massachusetts should discard the product.
HeartWare HVAD System Batteries are being recalled due to electrical faults that may prevent the battery from powering the device controller, accepting charges, or maintaining charge. Approximately 19,616 batteries distributed worldwide are affected.
Kingdom Creamery of Vermont LLC is recalling Rococo Ice Cream 15% base mix due to potential Listeria monocytogenes contamination. The recalled product was distributed in Vermont, Maine, and Massachusetts.
Albertsons Companies recalled Ready Meals Shrimp Cooked with Cocktail Sauce for undeclared fish and shellfish allergens. The product was distributed across 24 US states.
Kingdom Creamery of Vermont is recalling 14% Base Mix and Archie Case Mix ice cream base products due to Listeria monocytogenes contamination. A Class I FDA recall affects 1,623 cases distributed to Vermont, Maine, and Massachusetts.
Kingdom Creamery of Vermont is recalling 5% Vanilla Soft Serve Mix due to potential Listeria monocytogenes contamination. The affected product was distributed in Vermont, Maine, and Massachusetts.
Kingdom Creamery of Vermont LLC is recalling Lake Champlain Chocolates 14% base mix due to potential Listeria monocytogenes contamination. The product was distributed in Vermont, Maine, and Massachusetts.
Family Dollar is recalling CURAD First Aid Kits (SKU 999037) that were improperly stored without temperature control from April 30 to June 10, 2022. The temperature exposure may have degraded medications or compromised medical devices within the kits.
Myolyn Inc. is recalling the power electronic box subassembly for the MyoCycle MC-2 because internal mounting screws may come loose during shipping, creating a risk of electrical shock.
Luminex Corporation recalled 257 units of the ARIES SARS-CoV-2 Assay (lot AB4042A) due to potential false negative results. The assay may fail to detect the ORF1ab gene, risking missed COVID-19 infections.
Nephron Sterile Compounding Center is recalling 294 bags of Trisodium Citrate 0.5% Solution IV bags due to potential cross-contamination from manufacturing deviations. The affected lots were distributed nationwide.
GS Saline Solution (12 fl oz) was not stored in temperature-controlled areas, risking contamination. The affected product was sold at Family Dollar stores nationwide from May 1–June 10, 2022.
Kabobs Acquisition Inc. is recalling Truffle Arancini with Wild Mushrooms due to potential glass pieces in the rice. The product was distributed to multiple states.
Family Dollar is recalling LIFESTYLES ULTRA SENSITIVE CONDOMS 12CT that were stored without proper temperature control. Customers should discontinue use of product purchased between May 1 and June 10, 2022.
Simply Saline Nasal Mist 3.1 oz sold at Family Dollar stores has been recalled due to improper temperature storage between May and June 2022. Consumers should return the product to their local Family Dollar store.
ASO LLC is recalling 274,458 retail packages of three wound care products that fall apart during handling after removal from packaging, compromising their sterility and usability.
Clearblue Smart Countdown pregnancy tests distributed to Family Dollar stores were not stored in temperature-controlled conditions. Consumers who purchased this product should return it for a refund or replacement.
Nephron Sterile Compounding Center is recalling one lot of Neostigmine Methylsulfate Injection due to potential cross-contamination from product carryover during manufacturing. The recall affects 13,500 vials distributed nationwide.
Trinity Sterile is recalling Wolf Pak Premium Dressing Change Kits labeled as latex-free. The Non-Adherent Dressing component contains natural rubber latex, creating risk for patients with latex allergies.
Wolf-Pak Premium Dressing Kits labeled latex-free are being recalled because a component contains natural rubber latex, posing a risk to people with latex allergies.
Becton Dickinson recalls 9,340 units of BD PhaSeal Y-Site Connectors (Catalog 515304) due to incorrect expiration dates printed on product labels that extend beyond the actual product expiration.
Kabobs Acquisition Inc. is recalling Tomato, Basil & Mascarpone Arancini products due to possible glass contamination from their rice supplier. Affected lot numbers include PM22F23, PM22F30, and PM22G13.
Baxter Healthcare recalls 85,680 bags of acetaminophen injection nationwide due to temperature abuse in distribution. Product was shipped in refrigerated trucks despite being labeled for room temperature storage.
Trinity Sterile's Wolf Pak Premium Dressing Change Kit is mislabeled as latex-free but contains natural rubber latex in component 94-7002. This poses a risk to people with latex allergies.
Family Dollar is recalling SKYN Original, Elite, and LS non-latex condoms due to improper storage. Products sold between May 1 and June 10, 2022 were not stored in temperature-controlled conditions.