All recall categories

Recalls distributed in Massachusetts

These notices name Massachusetts in the distribution list the company gave its agency. That list says where the product was shipped, not where it ended up — a recalled item can travel with a shopper, and some notices list no states at all.

4,249 stored notices name Massachusetts, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,122 notices were distributed nationwide, so they reach Massachusetts too — those are in the archive.

Medical devices

Reported Jul 25, 2012

Infusomat(R) Space Pump (US Version) with software version 686G030103 (commonly termed 'G03'), 686E030003, 686F030005,…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

B. Braun Medical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 25, 2012

Integra(TM) Jarit(R) Take-Apart Endoscopic Instruments. Integra(TM) Jarit(R) Take-Apart Endoscopic Instruments are…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Integra Limited

FDA (openFDA device enforcement)

Medical devices

Reported Jul 25, 2012

Philips Brilliance 6, 16, 40, 64, Big Bore, iCT and iCT SP are Computed Tomography X-Ray Systems. The devices are…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Philips Medical Systems (Cleveland) Inc.

FDA (openFDA device enforcement)

Food

Reported Jul 25, 2012

SP Standard Process, Cataplex ACP (Product #0700 and 0750) , Dietary supplement, 90 & 360 Tablets, Proprietary Blend:…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Standard Process, Inc.

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jul 25, 2012

Terumo Advanced Perfusion System 1 System 1 Base, 100/120V. The Terumo Advanced Perfusion System 1 is indicated for use…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Terumo Cardiovascular Systems Corporation

14 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 18, 2012

CIVCO VirtuTRAX Instrument Navigator, Reusable non-sterile general purpose driveBAY, trakSTAR, electromagnetic sensor…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Civco Medical Instruments Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 18, 2012

GE Advantage CT/PET Fusion for Advantage Windows Workstation with Volume View CT Colonography/Navigator 2 software.…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

GE Healthcare, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jul 18, 2012

Philips HeartStart MRx M3536A Defibrillator/Monitor with Software R.03.03 The Heartstart MRx is for use for the…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Philips Healthcare Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 18, 2012

superDimension Systems AAS00016-xx with Software Version 4.0-4.9. Indicated for use for displaying images of the…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

superDimension, Inc.

FDA (openFDA device enforcement)

Food

Reported Jul 11, 2012

Hannaford brand Mini Frosted Cookies, 10 oz UPC # 4126872374

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Hannaford Bros.

FDA (openFDA food enforcement)

Medical devices

Reported Jul 11, 2012

Single Shot Epidural Trays, Sterile, Integra Pain Management, West Valley City, Utah 84119, each kit contains sterile…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Integra LifeSciences Corp. d.b.a. Integra Pain Management

FDA (openFDA device enforcement)

Medical devices

Reported Jul 11, 2012

TDX SP Power Wheelchair, TDX SR Power Wheelchair, TDX SI Power Wheelchair. Model Number(s): TDXSI, TDXSI-2, TDXSI-2-S,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Invacare Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Jul 11, 2012

Microbiologics 217 Osseo Avenue North, St. Cloud, MN 56303, Gram Stain Control Slides, SLO3-10, ATCC Licensed…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Microbiologics Inc.

FDA (openFDA device enforcement)

Food

Reported Jul 11, 2012

Rosati Cry Baby Sour Watermelon water ice, 6 fl oz

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

SR Rosati, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jul 4, 2012

BCS(R) Behring Coagulation System, Device catalog No. OVIO03 Product Usage: Multipurpose system for In Vitro…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Siemens Healthcare Diagnostics, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Jul 4, 2012

Organic 100% Pomegranate Juice packed in glass bottles Smart Juice Organic Pomegranate 100% Juice 33.8 FL. Oz. 100%…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Smart Juice LLC

FDA (openFDA food enforcement)

Medical devices

Reported Jun 27, 2012

Arrow International, Inc. 7FR 3-Lumen Arrowg+ard Blue Plus(R) Pressure Injectable Central Venous Catheter - Catalog…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Arrow International Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 27, 2012

Olympic Cool-Cap System is intended to provide treatment for neonatal hypoxic-ischemic encephalopathy (HIE). The…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Natus Medical Incorporated

FDA (openFDA device enforcement)

Medical devices

Reported Jun 27, 2012

SARNS HIGH-FLOW AORTIC ARCH CANNULA: 5.2 MM (16 FR) 00 WITH 3/8" CONNECTOR, 7.5" (19 CM) LONG. The Sarns High Flow…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Terumo Cardiovascular Systems Corporation

10 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jun 20, 2012

Bliss Bros. Dairy Chocolate Peanut Butter Cookie Dough Ice Cream, 3-gallon round paperboard,: frozen

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Bliss Bros Dairy, Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Food

Reported Jun 20, 2012

AlsoSalt Sodium Free Butter flavored Salt Substitute, 2.5 oz. bottle

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Diversified Natural Products, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jun 20, 2012

The Brilliance iCT and iCT SP are Computed Tomography X-Ray Systems intended to produce cross-sectional images of the…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Philips Medical Systems (Cleveland) Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 20, 2012

T5 Hytrel Zipper Toga. Product Usage: The togas are intended to provide a barrier between the operating room and the…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Stryker Instruments Div.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Jun 20, 2012

Liquid Peanut Butter Topping under the Brand name: Superior Nut Company, Murray's, Dairy Queen packaged in 6.5 lb., 45…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Superior Nut Co. Inc.

FDA (openFDA food enforcement)

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RecallNow is not a government agency. Every notice above was published by the FDA, USDA FSIS or CPSC and links back to its source. Browse the whole archive.