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Biogenex Laboratories

Biogenex Laboratories Recalls

All product recalls associated with Biogenex Laboratories.

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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 6881–6900 of 7756 recalls

Biogenex Laboratories: Anti-CD45 Cocktail antibody in 6 ml vials; Cat. No. AM371...

Mislabeling: Anti-CD45 cocktail antibody mislabeled as Ki-67.

FDASep 5, 2006TX• Biogenex Laboratories

Puritan Bennett Corporation: Puritan Bennett KnightStar 330 Bi-Level Ventilator, Catal...

Directions for Use-Puritan Bennett has determined that a service interval should be defined for the device. The firm has also determined that an exhalation filter should be employed when the device is in use.

FDAAug 31, 2006PR• Puritan Bennett Corporation

Beckman Coulter Inc: CXP Analysis Software, Versions 2.0 & 2.1: Part #722396 C...

Two workflow scenarios associated with renaming regions may produce incorrect results.

FDAAug 29, 2006Nationwide• Beckman Coulter Inc

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Beckman Coulter Inc: Cytomics FC 500 MPL with MXP software, Versions 2.0 & 2.1...

Two workflow scenarios associated with renaming regions may produce incorrect results.

FDAAug 29, 2006Nationwide• Beckman Coulter Inc

Beckman Coulter Inc: Cytomics FC 500 with CXP software, Versions 2.0 & 2.1: Pa...

Two workflow scenarios associated with renaming regions may produce incorrect results.

FDAAug 29, 2006Nationwide• Beckman Coulter Inc

Nicolet Biomedical Div of Viasys Healthcare: NicoletOne version 5.20 software (also known as NicoletOn...

A software anomaly exists in the 5.20.1038 NicoletOne LTM, Sleep, nEEG, vEEG and ICU Monitor systems using the M, and/or C series amplifiers. If this anomaly occurs, the system will display the data for channel one in all channels on NicoletOne LTM, Sleep, nEEG, vEEG or ICU Monitor systems.

FDAAug 25, 2006Nationwide• Nicolet Biomedical Div of Viasys Healthcare

Bemis Health Care, Inc: 5 Qt. Wallmount Sharps Container, Model 150, Regular Size...

The 5 Quart Wall Safes are shipped as two pieces (bottom & top) that customers are unable to assemble because of excess warp in the back wall of the container.

FDAAug 23, 2006Nationwide• Bemis Health Care, Inc

Lawnmower Blades (Blount) – replacement defect (2006)

Laceration Risk

The recalled replacement lawnmower blades are intended for use on Snapper riding lawnmowers. The recalled blades are sold for use as replacement parts under the Oregon® and Silver Streak® brands only. Original equipment blades on Snapper lawnmowers and "Snapper" brand replacement blades are not included in this recall. The recalled blades are red and marked "MADE IN USA," "GRASS SIDE CX", "Oregon" or "SILVER STREAK." The part number and date code are engraved on one side of the blade. The recalled blades are part numbers: 99-111, 99-112, 99-113, 99-114, 99-117, 99-118, 99-926, 99-930 and date codes: BL, BM, BN, BP, BQ, BR, BS, BT, BU, BV, BW, BX, BY, BZ, CA, CB, CC, CD, CE, CF, CG, CH, CJ, CK, CL, CM, CN, CP.

CPSCAug 23, 2006Nationwide• Blount International Inc., of Kansas City, Mo.

Cordless Electric Lawnmowers (Black & Decker) – fire hazard (2006)

Fire/Burn Risk

The mowers were sold under both the Black & Decker and Craftsman brand names. The recalled Black & Decker mowers have the model CMM1000 or CMM1000R and are labeled as Type 1 through Type 4, both of which are located on the silver and black label affixed to the rear door of the mower. Mowers labeled as Type 5 are not included in this recall. The Black & Decker mowers have either an orange or green deck with a black motor cover. The Craftsman brand mowers have model number 900.370520 and include all date codes and types. The model number is located on the silver and black label affixed to the rear door of the mower. The Craftsman mowers have a dark green deck with a black motor cover.

CPSCAug 16, 2006Nationwide• Black & Decker (U.S.) Inc., of Towson, Md.

Abbott Laboratories MPG: IMx Sirolimus Reagent Pack; list 5C91-21; 100 test pack c...

The sirolimus values may shift higher after storage at 2-8C or after one freeze/thaw cycle of specimens.

FDAAug 11, 2006PR• Abbott Laboratories MPG

Frameworx Chairs and Bar Stools (Brunswick) – unspecified risk (2006)

The recalled chairs and bar stools were sold under the model name Frameworx. The models affected are short table height chair model number 53-861025-000 and tall bar stool model number 57-860979-000. The model name and model numbers are not written on the chairs. The model number is only written on the original shipping carton, packing list or invoice. The chairs and bar stools have a plastic bucket-style seat bolted to a steel seat plate assembly that connects to the down tube of the seat.

CPSCAug 11, 2006Nationwide• Brunswick Bowling & Billiards Corp., of Lake Forest, Ill.

Cardinal Health 303 Inc DBA Alaris Products: Alaris SE Pump (formerly Signature Edition Infusion Pump)...

This recall was initiated because of a potential for over infusion with all models of the Alaris SE Pumps (formerly the Signature Edition Infusion Pumps) caused by key bounce.

FDAAug 10, 2006Nationwide• Cardinal Health 303 Inc DBA Alaris Products

ALEX Super Cooking Sets – laceration risk (2006)

Laceration Risk

This recall involves children's Super Cooking Sets, a 12-piece stainless steel set with miniature pots that have clear glass lids. Each set comes with a pasta pot with glass lid, stockpot with glass lid, frying pan, two potholders and utensils. The cooking sets were sold in a white box with a clear plastic window. "ALEX" and "Super Cooking Set" are printed on the box. A red sticker labeled "unbreakable glass" is affixed to the pot lids. Cooking sets manufactured after April 1, 2006 have stainless steel lids and are not included in this recall.

CPSCAug 10, 2006Nationwide• Panline USA Inc., doing business as ALEX, of Northvale, N.J.

Robertshaw Gas Controls – fire risk (2006)

Fire/Burn Risk

The FS Flame Switches and FM Automatic Safety Valves being recalled are installed on natural and liquid propane (LP) gas commercial cooking equipment, such as ranges, pasta cookers, deep fat fryers or griddles. The recalled FS Flame Switches were installed on the following commercial cooking equipment brands: Keating (of Chicago), PMI Food Equipment Group, Vulcan, Southbend, Blodgett, Toastmaster, and Wolf Range. The recalled FM Automatic Safety Valves were installed on the following commercial cooking equipment brands: Bari (Restaurant and Pizzeria), Southbend, and Blodgett. The model and/or serial numbers can be found on the cooking appliance identification plate located on the appliance. For a list of appliances with recalled switches and valves, visit www.robertshaw.com

CPSCAug 2, 2006Nationwide• Robertshaw Controls Co., of West Plains, Mo.

Trionix Research Laboratory Inc: BIAD Classic 24 (24 inch collimator). The collimator is a...

The ball screw on the unit which supports the detector head (which weighs approximately 800 lbs.) could snap resulting in the detector head dropping on the patient.

FDAAug 1, 2006Nationwide• Trionix Research Laboratory Inc

Beckman Coulter Inc: UniCel Dxl 800 Access Immunoassay Systems Wash Buffer, Pa...

The neck of the wash buffer cube can be extended higher than intended possibly causing the system to aspirate air instead of buffer before the buffer container is empty without the system immediately indicating that the supply is empty. This may lead to incorrect assay results.

FDAJul 28, 2006Nationwide• Beckman Coulter Inc

Beckman Coulter Inc: Cytomics FC 500 Flow Cytometry System with CXP Software V...

Mis-identification-If a panel or protocol is added to an existing worklist but the tube location is not specified, the CXP Acquisition software will run the last specified tube through the remaining protocols and will generate results and printouts of these runs leading to a Mis-Identification condition.

FDAJul 26, 2006Nationwide• Beckman Coulter Inc

Bunn Home Coffeemakers – burn and fire hazard (2006)

Fire/Burn Risk

The recall involves Bunn® home coffeemakers with model numbers GR-10B, GR-10W, B-10B, B-10W, and BT-10B (including any of those same model numbers ending in the additional letter D) with six-digit date codes (1) ending in "04" with the two middle digits between "21" and "52" or (2) ending in "05" with the two middle digits between "01" and "40". (If the date code has a seventh digit, consumers should ignore the last digit and use the first six digits.) The model number and date code are stamped on a small white or silver sticker on the bottom of the coffeemaker. The 10-cup Bunn® coffeemakers have either a black or white plastic base and top, and measure 14¼ inches high by 7 inches wide by 13¾ inches deep. The word "BUNN®" is printed on the front of the machine in chrome.

CPSCJul 25, 2006Nationwide• Bunn-O-Matic Corp., of Springfield, Ill.

Ciba Vision Corporation: Focus * DAILIES * Toric * One-Day Contact Lenses * CIBA V...

Misbranding; Lenses (-0.75) are labeled with the incorrect power of (-1.50) .

FDAJul 25, 2006Nationwide• Ciba Vision Corporation

Microvision Medical Holding B.V. Meibergdreef 45 Amsterdam Netherlands: MicroScan Lens Disposable Plastic Cap used with MicroScan...

Some lenses may have microscopic holes in the disposable caps representing a potential break in the sterile barrier

FDAJul 21, 2006CA, IN, IA +4 more• Microvision Medical Holding B.V. Meibergdreef 45 Amsterdam Netherlands