Stay Informed

Get email alerts when new recalls match your interests.

Recall data is updated hourly from official government sources. Very recent recalls may not yet appear. About our data sources

About

We make U.S. recall data searchable and accessible for consumers and businesses.

Site

FAQ
Browse by State
Statistics
Recall Classifications
About
Enterprise API

Legal

Privacy Policy
Terms of Service
Report Incorrect Info

Official Sources

FDA Recalls ↗
USDA FSIS ↗
CPSC Recalls ↗
NHTSA Recalls ↗

RSS Feed

Home
/
Brands
/
MWT Materials, Inc.

MWT Materials, Inc. Recalls

All product recalls associated with MWT Materials, Inc..

Get alerts for this brand

Recall Summary

Total Recalls

1000

Past Year

123

Class I (Serious)

Most Recent

Nov 2025

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 1681–1700 of 2383 recalls

MWT Materials, Inc.: Accusorb MRI MAC7007 Part Number: MRI-07 MRI-Breast S...

When not used correctly, Accusorb MRI products may overheat and lead to patient injury.

Class IIModerate

FDAOct 6, 2014Nationwide• MWT Materials, Inc.

MWT Materials, Inc.: Accusorb MRI MAC7030 Product Usage: Radio frequen...

When not used correctly, Accusorb MRI products may overheat and lead to patient injury.

Class IIModerate

FDAOct 6, 2014Nationwide• MWT Materials, Inc.

MWT Materials, Inc.: Accusorb MRI MAC7002 Part Number: MRI-02 MRI-Arm Slee...

When not used correctly, Accusorb MRI products may overheat and lead to patient injury.

Class II

1...83 848586 87...120

Page 85 of 120Next

Moderate

FDAOct 6, 2014Nationwide• MWT Materials, Inc.

MWT Materials, Inc.: Accusorb MRI MAC7003 Part Number: MRI-03 U (Upper) and...

When not used correctly, Accusorb MRI products may overheat and lead to patient injury.

Class IIModerate

FDAOct 6, 2014Nationwide• MWT Materials, Inc.

MWT Materials, Inc.: Accusorb MRI MAC7010 Product Usage: Radio frequen...

When not used correctly, Accusorb MRI products may overheat and lead to patient injury.

Class IIModerate

FDAOct 6, 2014Nationwide• MWT Materials, Inc.

MWT Materials, Inc.: Accusorb MRI MAC7009 Part Number: MRI-09 MRI- Leg Wra...

When not used correctly, Accusorb MRI products may overheat and lead to patient injury.

Class IIModerate

FDAOct 6, 2014Nationwide• MWT Materials, Inc.

MWT Materials, Inc.: Accusorb MRI MAC7004 Part Number: MRI-04 MRI-Poncho ...

When not used correctly, Accusorb MRI products may overheat and lead to patient injury.

Class IIModerate

FDAOct 6, 2014Nationwide• MWT Materials, Inc.

MWT Materials, Inc.: Accusorb MRI MAC7001 Part Number: MRI-01 MRI-Large Bl...

When not used correctly, Accusorb MRI products may overheat and lead to patient injury.

Class IIModerate

FDAOct 6, 2014Nationwide• MWT Materials, Inc.

MWT Materials, Inc.: Accusorb MRI MAC7006 Part Number: MRI-06 MRI-Large T...

When not used correctly, Accusorb MRI products may overheat and lead to patient injury.

Class IIModerate

FDAOct 6, 2014Nationwide• MWT Materials, Inc.

MWT Materials, Inc.: Accusorb MRI MAC7008 Part Number: MRI-08 MRI-Boot ...

When not used correctly, Accusorb MRI products may overheat and lead to patient injury.

Class IIModerate

FDAOct 6, 2014Nationwide• MWT Materials, Inc.

Cook Medical Incorporated: Spirotome" Soft-Tissue Biopsy Needle Set. The Spirotom...

MEDINVENTS, the manufacturer of the Spirotome" Soft-Tissue Biopsy Needle Set distributed by Cook Medical, has initiated a voluntary recall of these products. The recall has been initiated due to customer complaints that the protective caps were dislodged in the pouch. Further investigation disclosed potential dislodging of protective caps on the needle tips on other distributed products.

Class IIModerate

FDASep 26, 2014Nationwide• Cook Medical Incorporated

M&M's (Mars) - Undeclared Peanuts (2014)

Undeclared Nuts

Mars Chocolate North America is recalling M & Ms due to undeclared peanuts.

Class IIModerate

FDASep 19, 2014AZ, AR, CA +34 more• Mars Chocolate North America

Twix Unwrapped Bites (Mars) – Undeclared Allergens (2014)

Undeclared Nuts

Mars Chocolate North is recalling Twix Brand Unwrapped Bites 7 oz. pouch due to undeclared peanuts and eggs.

Class IHigh

FDASep 5, 2014Nationwide• Mars Chocolate North America

Avocados (Calavo Growers) – Salmonella Risk (2014)

Salmonella

Calavo Growers is recalling Avocados because they may be contaminated with Salmonella.

Class IHigh

FDASep 5, 2014IL, WA, WI• Calavo Growers, Inc. (Corporate)

Alprazolam Tablets (Sandoz) – metal particulates (2014)

Presence of Foreign Substance; tablets may contain stainless steel metal particulates

Class IIModerate

FDAJul 25, 2014Nationwide• Sandoz Incorporated

Dark Organic Chocolate Chip (Puratos) – milk protein allergen (2014)

Puratos initiated a recall due to an allergic reaction to milk protein, reported by a consumer.

Class IHigh

FDAJul 24, 2014CA, PA• Puratos Chocolate USA

Gambro Renal Products, Incorporated: Prismaflex HF 1400. Product number 107142. Each set is pa...

Gambro initiated a field action on the Prisma and Prismaflex sets due to breakages of connectors resulting in leakage of liquid or blood.

Class IIModerate

FDAJul 18, 2014Nationwide• Gambro Renal Products, Incorporated

Gambro Renal Products, Incorporated: Prisma HF1000 preset (new design). Product number 107639....

Gambro initiated a field action on the Prisma and Prismaflex sets due to breakages of connectors resulting in leakage of liquid or blood.

Class IIModerate

FDAJul 18, 2014Nationwide• Gambro Renal Products, Incorporated

Gambro Renal Products, Incorporated: PrisMARS Kit (component of MARS Treatment Kit Type 1115/1...

Gambro initiated a field action on the Prisma and Prismaflex sets due to breakages of connectors resulting in leakage of liquid or blood.

Class IIModerate

FDAJul 18, 2014Nationwide• Gambro Renal Products, Incorporated

Gambro Renal Products, Incorporated: X-MARS Set (component of MARS Treatment Kit Type 1116/1 ...

Gambro initiated a field action on the Prisma and Prismaflex sets due to breakages of connectors resulting in leakage of liquid or blood.

Class IIModerate

FDAJul 18, 2014Nationwide• Gambro Renal Products, Incorporated