Carroll-Baccari recalls

Carroll-Baccari has 6 recalls on record with the FDA and USDA, the earliest in 2019 and the latest reported on 1 Apr 2020. The most frequent reason is sterility.

Total recalls6since 2019

Last 12 months0reported

Class I00% of total

Ongoing0latest 1 Apr 2020

Recalls per month, last 24 months

click a bar for that month

0Oct '24 0 0 0Jan '25 0 0 0Apr 0 0 0Jul 0 0 0Oct 0 0 0Jan '26 0 0 0Apr 0 0 0Jul 0 0

Severity split

Class I 0 0%Class II 6 100%Class III 0 0%

Why carroll-baccari is recalled

Sterility467%
Other Reasons233%

Product types

Other Medical Devices467%
Patient Monitors233%

By year

2020467%
2019233%

All carroll-baccari recalls, newest first

6 total

Reported	Class	Recall	Company	Reason	Where
1 Apr 2020Device	CLASS II	Mvap Medical Supplies Inc, Mavidon CardioPrep Single recalled	Carroll-Baccari	Sterility	Nationwide
1 Apr 2020Device	CLASS II	PediaPrep Tubes (MD0033-T) and Single use cups (MD0033-SUP) recalled	Carroll-Baccari	Sterility	Nationwide
1 Apr 2020Device	CLASS II	Wave Prep Tubes (1710-03) and single use cups (17--00-24) recalled	Carroll-Baccari	Sterility	Nationwide
1 Apr 2020Device	CLASS II	LemonPrep Tubes (MD0019-T) and Single use cups (MD0019-SUP) recalled	Carroll-Baccari	Sterility	Nationwide
20 Nov 2019Device	CLASS II	Lemon Prep: MD0019T - tubes MD0019--SUP recalled by Carroll-Baccari	Carroll-Baccari	Other	FL
20 Nov 2019Device	CLASS II	Pedia Prep: MD0033T - tubes MD0033--SUP recalled by Carroll-Baccari	Carroll-Baccari	Other	FL

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.