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
/
Cytocell Ltd. 418 Cambridge Science Park, Milton Road Oxford Gene Technology Cambridge United Kingdom

Cytocell Ltd. 418 Cambridge Science Park, Milton Road Oxford Gene Technology Cambridge United Kingdom Recalls

All product recalls associated with Cytocell Ltd. 418 Cambridge Science Park, Milton Road Oxford Gene Technology Cambridge United Kingdom.

Get alerts for this brand

Recall Summary

Total Recalls

1000

Past Year

567

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 2661–2680 of 7756 recalls

Cytocell Ltd. 418 Cambridge Science Park, Milton Road Oxford Gene Technology Cambridge United Kingdom: CytoCell DiGeorge/VCFS TUPLE1 Region and 22q13.3 Region P...

The device may show unexpected locus specific signals in addition to those at 22q. Users may observe faint additional locus specific signals at 20p12/13.

FDAMay 17, 2021CA, IL, MO +4 more• Cytocell Ltd. 418 Cambridge Science Park, Milton Road Oxford Gene Technology Cambridge United Kingdom

Brainlab AG Olof-palme-str. 9 Munich Germany: ExacTrac Dynamic software, Model 20910-01B ETD Positionin...

Display of potential patient movement might be delayed to the user for high dose treatments.

FDAMay 14, 2021Nationwide• Brainlab AG Olof-palme-str. 9 Munich Germany

Ski-Doo Snowmobiles (BRP) – fire hazard (2021)

Fire/Burn Risk

This recall involves model year 2021 and 2022 Ski-Doo Backcountry, Expedition, MXZ, Renegade, Skandic and Tundra snowmobiles equipped with a 600 EFI engine. The vehicles were sold in a variety of colors. Ski-Doo and the model name are printed on the side panels of the vehicles. The vehicle identification number (VIN) is on the decal located on the right-hand side of tunnel. The following models are included in the recall: Model Year Model Name 2021 Ski-Doo Backcountry Sport 600 EFI 2021 Ski-Doo Expedition Sport 600 EFI 2021 Ski-Doo MXZ Sport 600 EFI 2021 and 2022 Ski-Doo Renegade Sport 600 EFI 2021 and 2022 Ski-Doo Skandic Sport 600 EFI 2021 and 2022 Ski-Doo Tundra Sport 600 EFI

1...132 133134135 136...388

Page 134 of 388Next

CPSCMay 13, 2021Nationwide• Bombardier Recreational Products Inc. of Canada

EpiGenius Kids Chocolate (Organic By Nature) – undeclared milk (2021)

Undeclared Milk

Product recalled due to undeclared milk in MCT powder used in manufacturing. Milk is not declared on the label. Product item #'s 4600-P65, 4600

Class IHigh

FDAMay 13, 2021Nationwide• Organic By Nature, Inc.

Log Splitters (Briggs & Stratton) – engine safety (2021)

The recall involves YTL, Longli and TIYA log splitters powered by Briggs & Stratton 250cc engine model number 15T232-0011-F8, with serial numbers 160331883074 through 2012073736714, and model number 15T232-1850-F1, with serial numbers 2004260782583 through 2012284118417. The engine's model number is printed on the valve cover and the engine's serial number is printed on the blower housing cover. The log splitters are sold under the following brands: Black Diamond (model number BDBS32T - 32 ton and YTL-015-134 - 30 ton); Crimson (model number YTL-590-012 - 32 ton); Lumberjack (model number YTL-007-414); Performance Built (model number YTL-007-308 and YTL-016-476 - 30 ton); Brute (model numbers YTL-140-701 - 30 ton and YTL-140-473 - 35 ton); Country Pro (YTL-019-880); Boss (model number WD32T); and Oregon (model 3000 Series - 30 ton).

CPSCMay 12, 2021Nationwide• Briggs & Stratton, of Wauwatosa, Wis. (engine)

Medically Minded Hand Sanitizer (Global) - Low Alcohol Content (2021)

Chemical Contamination: FDA analysis found 1 lot of MEDICALLY MINDED Hand Sanitizer Gel, ANTIMICROBIAL FORMULA (ethyl alcohol 70%) to be below the label claim for ethanol content and to contain methanol.

Class IHigh

FDAMay 12, 2021Nationwide• Global Sanitizers LLC

Hand Sanitizer Gel (Global Sanitizers) – Chemical Contamination (2021)

Class IHigh

FDAMay 12, 2021Nationwide• Global Sanitizers LLC

Medically Minded Hand Sanitizer (Global) - Manufacturing Deviation (2021)

CGMP Deviations: lots and products of hand sanitizer are being recalled because they were manufactured under the same conditions as the product lot found to contain methanol.

Class IIModerate

FDAMay 12, 2021Nationwide• Global Sanitizers LLC

Hand Sanitizer Gel (Global Sanitizers) – Manufacturing Issues (2021)

CGMP Deviations: lots and products of hand sanitizer are being recalled because they were manufactured under the same conditions as the product lot found to contain methanol.

Class IIModerate

FDAMay 12, 2021Nationwide• Global Sanitizers LLC

Hand Sanitizer Gel (Global Sanitizers) – Manufacturing Issues (2021)

CGMP Deviations: lots and products of hand sanitizer are being recalled because they were manufactured under the same conditions as the product lot found to contain methanol.

Class IIModerate

FDAMay 12, 2021Nationwide• Global Sanitizers LLC

Hand Sanitizer Gel with Aloe (Global Sanitizers) – Manufacturing Issues (2021)

CGMP Deviations: lots and products of hand sanitizer are being recalled because they were manufactured under the same conditions as the product lot found to contain methanol.

Class IIModerate

FDAMay 12, 2021Nationwide• Global Sanitizers LLC

DiBAR Labs Hand Sanitizer (DiBAR) – Manufacturing Issues (2021)

CGMP Deviations: Other lots and products of hand sanitizer recalled because they were manufactured under the same conditions as the product lots found to contain methanol.

Class IIModerate

FDAMay 11, 2021Nationwide• DIBAR NUTRICIONAL S DE RL DE CV

Advance Hand Sanitizer (DiBAR) – Manufacturing Issues (2021)

CGMP Deviations: Other lots and products of hand sanitizer recalled because they were manufactured under the same conditions as the product lots found to contain methanol.

Class IIModerate

FDAMay 11, 2021Nationwide• DIBAR NUTRICIONAL S DE RL DE CV

Hand Sanitizer (DiBAR Labs) – Chemical Contamination (2021)

Chemical Contamination: FDA analysis found 3 lots of DiBAR hand Sanitizer to be below the label claim for ethanol content and to contain methanol.

Class IHigh

FDAMay 11, 2021Nationwide• DIBAR NUTRICIONAL S DE RL DE CV

ProtectoRx Hand Sanitizer (DiBAR) – Manufacturing Issues (2021)

CGMP Deviations: Other lots and products of hand sanitizer recalled because they were manufactured under the same conditions as the product lots found to contain methanol.

Class IIModerate

FDAMay 11, 2021Nationwide• DIBAR NUTRICIONAL S DE RL DE CV

IMPLANTCAST GMBH Luneburger Schanze 26 Buxtehude Germany: EcoFit cup cementless: Model(Catalog Number)/Description...

A risk exists during impacting of the acetabular cup into the bone the plugs may come loose from the cup, which could lead to operation duration extension or revision operation. A warning note is being added to instructions for use and surgical technique alerting users that the quality of bone in the patient (such as osteosclerosis) is an attributable factor.

FDAMay 10, 2021Nationwide• IMPLANTCAST GMBH Luneburger Schanze 26 Buxtehude Germany

BioFire Diagnostics, LLC: BioFire BCID2 Panel, REF RFIT-ASY-0147, For FilmArray Sys...

Elevated rates of false negative results may occur when using blood culture panels due to issues in the manufacturing process. Pouches contained OPP from FilmArray Blood Culture Identification Panel (BCID) instead of OPP from BCID2 Panel.

FDAMay 10, 2021Nationwide• BioFire Diagnostics, LLC

Randox Laboratories Ltd. 55 Diamond Road Crumlin (North) Ireland: NEFA CAL (Non-Esterified Fatty Acids)- IVD Standard for m...

Standard packed within NEFA kit has been assigned incorrectly. Calibrating with the incorrect value will cause a positive shift of up to +8% with both quality controls and patient samples

FDAMay 10, 2021Nationwide• Randox Laboratories Ltd. 55 Diamond Road Crumlin (North) Ireland

Beckman Coulter Inc.: Access SARS-CoV-2 lgG II Calibrator, REF C69058, IVD, CE ...

SARS-CoV-2 lgG II numerical results may potentially be multiplied by a factor of 1000 on systems running with assay protocol file (APF) and access assay file (AAF) versions resulting in falsely elevated numerical values.

FDAMay 7, 2021AL, AK, AZ +28 more• Beckman Coulter Inc.

Beckman Coulter Inc.: Access SARS CoV-2 lgG II Reagent, REF: C69057, IVD CE UDI...

FDAMay 7, 2021AL, AK, AZ +28 more• Beckman Coulter Inc.