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MALVERN PANALYTICAL LTD Grovewood Road Malvern United Kingdom

MALVERN PANALYTICAL LTD Grovewood Road Malvern United Kingdom Recalls

All product recalls associated with MALVERN PANALYTICAL LTD Grovewood Road Malvern United Kingdom.

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Recall Summary

Total Recalls

1000

Past Year

891

Class I (Serious)

124

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 4301–4320 of 17593 recalls

NanoSight LM10 (Malvern Panalytical) – Laser Safety Non-Compliance (2022)

Product found to not comply to Class 1 Laser safety requirement.

Moderate

FDAFeb 28, 2022Nationwide• MALVERN PANALYTICAL LTD Grovewood Road Malvern United Kingdom

Medtronic InterStim Therapy System (Medtronic) – Software Data Issue (2022)

There is a software anomaly with the InterStim X Clinician software application with results in the data entered in the Patient Information fields not e retained and a " Data Lost" notification being displayed.

Moderate

FDAFeb 28, 2022Nationwide• Medtronic Neuromodulation

Regard IV Start Kit (Resource Optimization) – Swab Recall (2022)

A kit component, the PDI Prevantics Swab, was recalled.

Moderate

FDA

1...214 215216217 218...880

Page 216 of 880Next

Feb 28, 2022

IN, MO

• Resource Optimization & Innovation LLC

ExacTrac Dynamic Software (Brainlab) – Positioning Angle Error (2022)

The yaw angle may be incorrect for CBCT positioning workflows using setup beams with Varian LINACs.

Moderate

FDAFeb 25, 2022AZ, AR, CA +17 more• Brainlab AG Olof-palme-str. 9 Munich Germany

Protekt Sharps Safety Knives (Diamatrix) – Incorrect Handle Description (2022)

Surgical knives may contain incorrect description printed on handles. Specifically, some surgical knife handles may contain a size of "2.5mm" when the actual size is "2.2mm".

Moderate

FDAFeb 24, 2022Nationwide• International Science & Technology, LP, DBA Diamatrix Ltd.

iTotal Identity Posterior Stabilised (PS) Knee Replacement (Conformis) – incorrect tibial base pl...

Incorrect tibial base plate implant packaged in kit

High

FDAFeb 22, 2022MS• Conformis, Inc.

Cardiohelp-i Transport Guard (Maquet) – locking mechanism risk (2022)

Potential for a loose cylindrical pin on the Transport Guard that may result in the jamming of the locking mechanism causing the Transport Guard to not open or, if the locking pin is fully disengaged from the assembly, a full disassembly of the Transport Guard may occur, resulting in a delay of support if a product exchange is necessary.

High

FDAFeb 18, 2022Nationwide• Maquet Medical Systems USA

ORAcollect RNA (DNA Genotek) – liquid evaporation issue (2022)

Evaporation of stabilizing liquid reducing shelf life.

Low

FDAFeb 18, 2022Nationwide• DNA Genotek Inc. 3000-500 Palladium Dr Kanata Canada

ORAcollect Dx (DNA Genotek) – liquid evaporation issue (2022)

Evaporation of stabilizing liquid reducing shelf life.

Low

FDAFeb 18, 2022Nationwide• DNA Genotek Inc. 3000-500 Palladium Dr Kanata Canada

Snowmobiles (Polaris) - Crash Hazard (2022)

This recall involves certain VINs of Model Year 2022 MATRYX RMK, INDY, SWITCHBACK, VOYAGEUR, and NORDIC PRO snowmobiles. The recalled snowmobiles were sold in the following color combinations: black/titanium, red/black, blue/white/red, black/gray/blue, gray/lime, red/black/white, navy/silver/white, white/black/plum, tan/black/orange, gray/black/lime, gray/black/red, orange, black and jade. Polaris and model name are printed on the chassis on both sides of the vehicles. The model year and VIN are stamped on the right side of the tunnel. Consumers can enter their VIN at www.polaris.com/en-us/off-road-recalls/to see if your vehicle is included in any recalls.

High

CPSCFeb 17, 2022Nationwide• Polaris Industries Inc., of Medina, Minnesota

Children's Sleepwear (Esme) – Burn Hazard (2022)

Fire/Burn Risk

This recall involves four different styles of children's sleepwear garments; bunny, cherry, unicorn and shimmer sweets prints made of modal, cotton and spandex. The children's sleepwear was sold in sizes 12 months to 14 years. Children's sleepwear with the style number beginning with SF9 and a cut number of 1812, 2730, 7082 or 7104 printed on a label behind the garment's size and care labeling are included in the recall. Garment Description Size Range Price Bunny Print Style Number SF977 Cut Number 7082 Long Sleeve Top/Pant Pajama Set 47%Modal 47%cotton 6%spandex 12 Months, 18-24 Months, 2T, 3T, 4T, 5, 6, 7, 8, 9, 10, 12, and 14 $47 - $65 Cherry Print Style Number SF937/57 Cut Number 2730 Short Sleeve/Crop Legging Pajama Set 47%Modal 47%cotton 6%spandex 2T, 3T, 4T, 5, 6, 7, 8, 9, 10, 12, and 14 $50 - $63 Unicorn Print Style Number SF900/57 Cut Number 1812 Cami/Legging Pajama Set 47%Modal 47%cotton 6%spandex 2T, 3T, 4T, 5, 6, 7, 8, 9, 10, 12, and 14 $48 - $61 Shimmer Sweets Print Style Number SF950/57 Cut Number 7104 3 /4 Sleeved Top and Pant Pajama Set 47%Modal 47%cotton 6%spandex 2T, 3T, 4T, 5, 6, 7, 8, 9, 10, 12, and 14 $50 - $64

High

CPSCFeb 16, 2022Nationwide• Bottoms R US Inc, d/b/a Esme, of City of Industry, California

IRISpec Control (Beckman Coulter) – glucose test failure (2022)

IRISpec CA failures for glucose.

Moderate

FDAFeb 16, 2022Nationwide• Beckman Coulter, Inc.

5 Series Gas Ranges (Viking) – Gas Leak Risk (2022)

Fire/Burn Risk

This recall involves Viking Range Freestanding 5 Series Gas Ranges (models VGR and VGIC) manufactured between August 10, 2021 and December 1, 2021 and sold in stainless steel, white, and 14 other contemporary colors, which can be found at www.vikingincolor.com/the-contemporary-colors. The ranges were sold in various surface configurations including all burners or burners with griddle and/or grill. Units with model numbers and the following prefixes and serial numbers beginning with the following date codes are included in this recall: Model Numbers Serial Number Date Codes VGR5304B From 081021 to 120121 VGR5366B From 081021 to 120121 VGR5364G From 081021 to 120121 VGR5488B From 081021 to 120121 VGR5486G From 081021 to 120121 VGR5606GQ From 090221 to 120121 VGIC53024B From 081021 to 120121 VGIC53626B From 081021 to 120121 The model number for each unit is followed by a two-letter abbreviation that indicates the color of the unit. All colors, burner configurations, and gas types designated at the end of the model number are included. For example, base model VGIC53024B may include white units set for propane which would be VGIC53024BWHLP. The first six numeric characters in the serial number represent the manufacturing date. For example, a range with serial number 082421C10019872 was produced August 24, 2021. The model and serial numbers can be found on a label in one of three locations: On the left side panel under the left front grate support/burner bowl, on the front of the oven cavity face frame below the control panel, or on the bottom of the control panel above the door. Consumers should not search for the model and serial number when the range is hot.

High

CPSCFeb 16, 2022Nationwide• Viking Range LLC, of Greenwood, Miss.

Olanzapine Tablets (Macleods Pharma) – CGMP Deviation (2022)

cGmp Deviations

Class IIModerate

FDAFeb 16, 2022Nationwide• Macleods Pharma Usa Inc

Utility Vehicles EV, L3, L4, L5 (American Landmaster) – crash hazard (2022)

This recall involves American Landmaster utility vehicles series EV, L3, L4, L5, L5W and L7, equipped with standard (non-power) steering, and manufactured between March 2021 and October 2021. They were sold in red, blue and camouflage colors. Landmaster and the model name appear on the frame near the front left wheel of the vehicles. The model year and date of manufacture can be found on a data plate behind the vehicle's pedals.

High

CPSCFeb 16, 2022Nationwide• ASW LLC, d/b/a American Landmaster, of Columbia City, Ind.

Cookie Dough Ice Cream (Albertsons) – Undeclared Nuts (2022)

Signature Select Black Walnut Ice Cream was inadvertently packed in Cookie Dough container that does not declare nuts as allergen. Top lid correctly identified Black Walnut flavor.

Class IIModerate

FDAFeb 16, 2022CA• Albertsons Companies LLC

ProteusPLUS (Ion Beam) – proton beam pause verification (2022)

When resuming from a beam pause, the Proton Therapy System does not verify whether the beam range has not been manually modified during the pause and is still the prescribed one. Therefore, if an operator manually modified the range during a pause, there is a risk that a portion of the treatment beam after the resume is delivered with an error in range

High

FDAFeb 15, 2022FL, IL, KS +9 more• Ion Beam Applications S.A. Chemin Du Cyclotron 3 Louvain-la-neuve Belgium

Amlodipine Olmesartan Tablets (Macleods Pharma) – CGMP Deviation (2022)

cGMP deviations

Class IIModerate

FDAFeb 15, 2022Nationwide• Macleods Pharma Usa Inc

8 Square Template Slides (Cytocell) – incorrect expiry date (2022)

Labelled with an incorrect expiry date on the outer label with an extended expiry date than the validated shelf life. The correct expiry date for the device is 2022-02 and not 2023-05 as shown on the outer label.

Low

FDAFeb 14, 2022Nationwide• Cytocell Ltd. 418 Cambridge Science Park, Milton Road Oxford Gene Technology Cambridge United Kingdom

Norepinephrine Bitartrate (BayCare) – Subpotent Drug (2022)

Subpotent drug

Class IIILow

FDAFeb 14, 2022FL• BayCare Integrated Service Center, LLC /dba BayCare Central Pharmacy