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
/
Phadia Ab Rapsgatan Plant Rapsgatan 7 Uppsala Sweden

Phadia Ab Rapsgatan Plant Rapsgatan 7 Uppsala Sweden Recalls

All product recalls associated with Phadia Ab Rapsgatan Plant Rapsgatan 7 Uppsala Sweden.

Get alerts for this brand

Recall Summary

Total Recalls

1000

Past Year

566

Class I (Serious)

Most Recent

Jan 2026

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 3981–4000 of 7756 recalls

Phadia Ab Rapsgatan Plant Rapsgatan 7 Uppsala Sweden: Phadia" 1000 Model # 12-3800-01 Product Usage: The i...

code 7-102 Liquid Sensor Error

FDAJul 9, 2019Nationwide• Phadia Ab Rapsgatan Plant Rapsgatan 7 Uppsala Sweden

Voco GmbH Anton-Flettner-Str. 1-3 Cuxhaven Germany: Grandio SO Heavy Flow Caps, Color A3 - Product Usage: Fil...

The metal cannula are potentially too loose and may become loose when applying the filing material.

FDAJul 9, 2019IN, IA, NY• Voco GmbH Anton-Flettner-Str. 1-3 Cuxhaven Germany

Drospirenone Ethinyl Estradiol Tablets (Jubilant Cadista) – Failed Dissolution (2019)

Failed dissolution specifications : failed results at the 3-month stability time point.

Class IHigh

1...198 199200201 202...388

Page 200 of 388Next

FDA

Jul 9, 2019

Nationwide

• Jubilant Cadista Pharmaceuticals, Inc.

Heidelberg Engineering GmbH Tiergartenstr. 15 Heidelberg Germany: SPECTRALIS with HEYEX2 image management system. a non-c...

Error in the default configuration which could lead to the incorrect display of patient master data.

FDAJul 3, 2019Nationwide• Heidelberg Engineering GmbH Tiergartenstr. 15 Heidelberg Germany

Cincinnati Sub-Zero Products LLC, a Gentherm Company: Blanketrol III Hyper-Hypothermia System- body hypothermia...

Warnings statements have been added- exceeding 40 degree C for extended periods may cause tissue damage. Additionally, a caution was added and clarifications were made regarding the use of the Automatic modes

FDAJul 2, 2019Nationwide• Cincinnati Sub-Zero Products LLC, a Gentherm Company

Cincinnati Sub-Zero Products LLC, a Gentherm Company: CoolBlue Hyper-Hypothermia System- body hypothermia syste...

FDAJul 2, 2019Nationwide• Cincinnati Sub-Zero Products LLC, a Gentherm Company

Cincinnati Sub-Zero Products LLC, a Gentherm Company: Blanketrol II Hyper-Hypothermia System, Models 222R and ...

FDAJul 2, 2019Nationwide• Cincinnati Sub-Zero Products LLC, a Gentherm Company

RockShox Front Suspension Forks – Crash Hazard (2019)

This recall involves RockShox Lyrik and RockShox Yari front suspension forks with serial numbers 02T95514009 through 08T96214665. A bicycle fork is the part that holds the front wheel. The recalled forks are black or black and red and are for 29" bicycle wheels. RockShox is printed on the side of the fork and casting code 18 and O or 19 and A is embossed inside the webbing of the arch. The serial number can be found on the rear of the fork crown. The forks were sold as aftermarket equipment and as original equipment on the following mountain bicycle brands and models: BRAND MODEL Kona Process153 29 Process 153 DL 29 Process 153 CR 29 Process 153 CR DL 29 Process 165 29 Santa Cruz Megatower 29 Trek Powerfly LT 7 US Powerfly LT 9.7 US Scott Ransom 930

CPSCJul 2, 2019Nationwide• Sandleford Limited Taiwan Branch, of Taiwan

Privapath Diagnostics Ltd Unit A10 Block A Calmount Park; Calmount Avenue Dublin: Universal Sexual Health Testing Kit

A supplier informed PrivaPath Diagnostics that there is a potential for damaged tubes which could result in blood exposure or erroneous results due to an inappropriate blood-to-additive ratio.

FDAJul 1, 2019Nationwide• Privapath Diagnostics Ltd Unit A10 Block A Calmount Park; Calmount Avenue Dublin

Degania Silicone, Ltd. Degania Bet Dganya Bet Israel: Medline Silicone Drain 15Fr 3/16" Full Fluted PN: DYNJW...

15FR and 19FR round fluted drain channel drain may break during use (mostly during removal) in connection point between clear tube and white profile part. requiring additional surgical intervention to remove the broken end from patient's body

FDAJun 28, 2019Nationwide• Degania Silicone, Ltd. Degania Bet Dganya Bet Israel