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Sechrist Industries Inc

Sechrist Industries Inc Recalls

All product recalls associated with Sechrist Industries Inc.

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Recall Summary

Total Recalls

1000

Past Year

Class I (Serious)

Most Recent

Nov 2025

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 2201–2220 of 2399 recalls

Sechrist Industries Inc: Sechrist Monoplace Hyperbaric Chamber with Electronic Con...

Sechrist conducted a field upgrade on the hyperbaulic chambers equipped with Electronic Control Modules in order to correct a software bug that could potentially affect the performance of the chamber.

FDAAug 28, 2008Nationwide• Sechrist Industries Inc

Sechrist Industries Inc: Sechrist Monoplace Hyperbaric Chamber with Electronic Con...

Class IIModerate

FDAAug 28, 2008Nationwide• Sechrist Industries Inc

Sechrist Industries Inc: Sechrist Monoplace Hyperbaric Chamber with Electronic Con...

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Class IIModerate

FDAAug 28, 2008Nationwide• Sechrist Industries Inc

BD Diagnostics (GeneOhm Sciences, Inc): BD GeneOhm MRSA 200 ct, Catalog #441242. IDI-MRSA assay...

BD Diagnostics GeneOhm (BDDG) initiated the recall after they identified that the product has the potential to identify a patient as falsely positive for colonization with methicillin resistant Staphylococcus aureus. The potential health hazard related to a false positive result from this assay would be that a patient may be misclassified as having MRSA colonization when in fact they do not have

FDAJul 21, 2008Nationwide• BD Diagnostics (GeneOhm Sciences, Inc)

BD Diagnostics (GeneOhm Sciences, Inc): BD GeneOhm MRSA 48 ct, Catalog #441244. IDI-MRSA assay i...

FDAJul 21, 2008Nationwide• BD Diagnostics (GeneOhm Sciences, Inc)

Medical Device Technologies, Inc.: Angiotech, Bone Marrow Harvest Needle, Medical Device Tec...

Product packaging for Bone Biopsy trays/blisters may have a hole in the formed tray.

FDAJul 16, 2008Nationwide• Medical Device Technologies, Inc.

Medical Device Technologies, Inc.: Angiotech, Bone Marrow Aspiration Needle, Medical Device ...

Product packaging for Bone Biopsy trays/blisters may have a hole in the formed tray.

FDAJul 16, 2008Nationwide• Medical Device Technologies, Inc.

Medical Device Technologies, Inc.: Angiotech, T-Lok Bone Marrow Biopsy Needle, Medical Devic...

Product packaging for Bone Biopsy trays/blisters may have a hole in the formed tray.

FDAJul 16, 2008Nationwide• Medical Device Technologies, Inc.

Medical Device Technologies, Inc.: Angiotech, Bone Marrow Biopsy Needle, Medical Device Tech...

Product packaging for Bone Biopsy trays/blisters may have a hole in the formed tray.

FDAJul 16, 2008Nationwide• Medical Device Technologies, Inc.

Camouflage Pajama Sets (The Children's Place) – lead exposure (2008)

This recall involves long- and short-sleeved pajama sets. The sets have a blue shirt with a red screen print that reads "Athletics 90" and coordinating camouflage pants. The pajama sets were sold in boys' sizes XXS (2/3) to XL (14).

CPSCJun 10, 2008Nationwide• The Children's Place Retail Stores Inc., of Secaucus, N.J.

EMD Chemicals Inc: Histochemical PAS (Periodic Acid Schiff) Reaction Set' Cl...

Two complaints that kit was not performing properly with positive controls.

FDAJun 2, 2008Nationwide• EMD Chemicals Inc

Polymer Technology Systems, Inc.: PTS Panels LDL Cholesterol test strips for professional u...

The expiration date was extended by 20 weeks without justification.

FDAMay 29, 2008Nationwide• Polymer Technology Systems, Inc.

IntelliSwitch Fireplace Controls - Temperature Hazard (2008)

Fire/Burn Risk

This recall involves WSK-300 IntelliSwitch Fireplace Wall Controls sold with Heat & Glo gas direct vent fireplaces with the following model & serial numbers: Model Number Sales period All serial numbers up to 6000GLX-IPI-S January 2007 to January 22, 2008 0021279289 6000GLX-IPILP-S January 2007 to January 22, 2008 0021279322 6000GLX-IPI-R January 2007 to January 28, 2008 0021281203 6000GLX-IPILP-R January 2007 to January 22, 2008 0021279291 Cerona 36 January 2007 to January 22, 2008 0021279592 Cerona 42 January 2007 to January 23, 2008 0021279097 The fireplaces have a serial plate located on the floor, right hand side, of the fireplace control compartment. The model code, serial number, and date of manufacture are on this plate. The recall also includes the following wall controls sold separately: Wall Control Model Number Sales period All serial numbers Heat & Glo WSK-300-HNG January 2007 to December 2007 None Heatilator WSK-300-HTL June 2007 to December 2007 None Quadra-Fire WSK-300-QF November 2007 to December 2007 None

CPSCMay 28, 2008Nationwide• Hearth & Home Technologies Inc., of Lakeville, Minn. (Fireplace)

Gel Candles (M & A Global) - Fire Risk (2008)

Fire/Burn Risk

This recall involves Everlasting Jelly candles. Models include Champagne Glass with Heart, Model #502; Large Oval Bowl with Sand & Shells, Model #109-XL; Tumbler with Sand & Shells, Model #101-S; Round Shape with Curly Top and Red Roses, Model #506; Round Shape with Penguins, Model #604; Tumbler with Blue Roses & Leaves, Model #805-11; and Round Shape with Two Butterflies, Model #806-8. The candles were sold in clear glass containers of various sizes with a smaller glass of gel in the middle of the candle.

CPSCMay 23, 2008Nationwide• M & A Global Technologies Inc., doing business as Spa at Home, of Tallahassee, Fla.

Kenmore Wall Ovens (Frigidaire) – fire risk (2008)

Fire/Burn Risk

This recall involves Kenmore 24-inch-wide gas and propane, wall-mounted ovens. The self-cleaning ovens were sold in white, black, bisque and stainless steel, and have the Kenmore name printed on the oven control panel. The model and serial numbers of the ovens that are part of this recall can be found on the frame on the left side of the oven cavity. Model Numbers 790.30472400, 790.30473400, 790.30473401, 790.30474400, 790.30479400 Serial Number Range NF401xxxxx through NF610xxxxx

CPSCMay 20, 2008Nationwide• Frigidaire Canada, a sister company of Electrolux Home Products Inc., of Cleveland, Ohio

Hitachi Medical Systems America Inc: EUB-9500/HI VISION 8500 Diagnostic Ultrasound Scanners, ...

The firm's parent company discovered a DICOM UID (Universal Identifier) code mix-up which can occur due to a software error. This error can cause the images from two (2) different patient scans to become intermingled and consequently, labeled incorrectly.

FDAMay 12, 2008AR, CA, IN +1 more• Hitachi Medical Systems America Inc

Hitachi Medical Systems America Inc: EUB-6500/HI VISION 6500 Diagnostic Ultrasound Scanners, D...

FDAMay 12, 2008AR, CA, IN +1 more• Hitachi Medical Systems America Inc

SagaTech Electronics, Inc.: Finger Sensor for Remmers Recorder (Formerly SnoreSat Sle...

The outer jacket is receding away from the black sensor prematurely.

Class IIModerate

FDAMay 8, 2008Nationwide• SagaTech Electronics, Inc.

SagaTech Electronics, Inc.: Finger Sensor for Remmers Recorder (Formerly SnoreSat Sle...

The outer jacket is receding away from the black sensor prematurely.

FDAMay 8, 2008Nationwide• SagaTech Electronics, Inc.

Medical Device Technologies, Inc.: Hawkins III Breast Localization Needle. Product number 24...

The sterility of the product cannot be guaranteed.

FDAMay 6, 2008Nationwide• Medical Device Technologies, Inc.