Maine Recalls
2,937 recalls on record affecting Maine
GE Healthcare, LLC recalls Prestige II
GE Healthcare is conducting a recall due to the potential fall of aged CRT monitors - Prestige 2, Prestilix, Prestige VH, Prestige SI, RFX/SFX, Legacy, Precision 500D, ADVANTX and Innova 2000 systems.
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GE Healthcare, LLC recalls SFX
GE Healthcare is conducting a recall due to the potential fall of aged CRT monitors - Prestige 2, Prestilix, Prestige VH, Prestige SI, RFX/SFX, Legacy, Precision 500D, ADVANTX and Innova 2000 systems.
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GE Healthcare, LLC recalls ADVANTX LCN+
GE Healthcare is conducting a recall due to the potential fall of aged CRT monitors - Prestige 2, Prestilix, Prestige VH, Prestige SI, RFX/SFX, Legacy, Precision 500D, ADVANTX and Innova 2000 systems.
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GE Healthcare, LLC recalls ADVANTX LCLP+
GE Healthcare is conducting a recall due to the potential fall of aged CRT monitors - Prestige 2, Prestilix, Prestige VH, Prestige SI, RFX/SFX, Legacy, Precision 500D, ADVANTX and Innova 2000 systems.
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GE Healthcare, LLC recalls Legacy
GE Healthcare is conducting a recall due to the potential fall of aged CRT monitors - Prestige 2, Prestilix, Prestige VH, Prestige SI, RFX/SFX, Legacy, Precision 500D, ADVANTX and Innova 2000 systems.
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GE Healthcare, LLC recalls Innova 2000
GE Healthcare is conducting a recall due to the potential fall of aged CRT monitors - Prestige 2, Prestilix, Prestige VH, Prestige SI, RFX/SFX, Legacy, Precision 500D, ADVANTX and Innova 2000 systems.
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GE Healthcare, LLC recalls Prestilix
GE Healthcare is conducting a recall due to the potential fall of aged CRT monitors - Prestige 2, Prestilix, Prestige VH, Prestige SI, RFX/SFX, Legacy, Precision 500D, ADVANTX and Innova 2000 systems.
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GE Healthcare, LLC recalls ADVANTX LCV+
GE Healthcare is conducting a recall due to the potential fall of aged CRT monitors - Prestige 2, Prestilix, Prestige VH, Prestige SI, RFX/SFX, Legacy, Precision 500D, ADVANTX and Innova 2000 systems.
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GE Healthcare, LLC recalls RFX
GE Healthcare is conducting a recall due to the potential fall of aged CRT monitors - Prestige 2, Prestilix, Prestige VH, Prestige SI, RFX/SFX, Legacy, Precision 500D, ADVANTX and Innova 2000 systems.
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GE Healthcare, LLC recalls Prestige SI
GE Healthcare is conducting a recall due to the potential fall of aged CRT monitors - Prestige 2, Prestilix, Prestige VH, Prestige SI, RFX/SFX, Legacy, Precision 500D, ADVANTX and Innova 2000 systems.
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GE Healthcare, LLC recalls ADVANTX LCA
GE Healthcare is conducting a recall due to the potential fall of aged CRT monitors - Prestige 2, Prestilix, Prestige VH, Prestige SI, RFX/SFX, Legacy, Precision 500D, ADVANTX and Innova 2000 systems.
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GE Healthcare, LLC recalls Precision 500D
GE Healthcare is conducting a recall due to the potential fall of aged CRT monitors - Prestige 2, Prestilix, Prestige VH, Prestige SI, RFX/SFX, Legacy, Precision 500D, ADVANTX and Innova 2000 systems.
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GE Healthcare, LLC recalls Prestige VH
GE Healthcare is conducting a recall due to the potential fall of aged CRT monitors - Prestige 2, Prestilix, Prestige VH, Prestige SI, RFX/SFX, Legacy, Precision 500D, ADVANTX and Innova 2000 systems.
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Acumedia Manufacturers, Inc. recalls Tryptic Soy Agar, Acumedia PN 7100 500g, 2Kg, 10Kg, and 50K
light precipitate may form in prepared plates of Acumedia Tryptic Soy Agar (7100) Lot# 108166. While there is no change in growth performance of this medium, the formation of particulate matter may be misinterpreted as growth in poured plates thereby leading to inaccurate counts.
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On-X Life Technologies, Inc. recalls Chord-X Chordal Sizer is designed to assist in determining t
Four issues were uncovered by the recalling firm's CAPA: 1) Burrs were found to be present on Left Housing, Right Housing and Barrel components, 2) Loose plastic particulate was found within sealed primary packages, 3) Loose hair was discovered within four sealed primary packages and 4) Assembly error, wherein Left and Right Housing components were acceptably press-fit together, was discovered within one sealed primary package. One of the Left Housing press-fit pins was not pressed into the associated hole of the Right Housing, resulting in a small gap in the housing assembly.
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Implant Direct Sybron Manufacturing, LLC recalls SwishTapered Implant
The extender product code (9037-03) that is packaged with the SwishTapered (Part Number 933308; Lot Number 73241) Implant was packaged in the incorrect position. This discrepancy may lead to the possibility of extender not seating properly on the implant, which may lead to micro-leakage and a possible infection to the patient.
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Invacare Corporation recalls Foot Section - BAR5490IVC
A quality issue with the junction box used in the bariatric bed junction that may omit sparks and result into a fire.
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Invacare Corporation recalls Bariatric Bed - BAR600IVC
The junction box used in the bariatric bed may emit sparks and result in a fire.
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Invacare Corporation recalls Junction Box - 1104343 and 1193560
A quality issue with the junction box used in the bariatric bed junction that may omit sparks and result into a fire.
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Invacare Corporation recalls Bariatric Bed - BARPKG-IVC 1633
A quality issue with the junction box used in the bariatric bed junction that may omit sparks and result into a fire.
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Showing 20 of 2,937 recalls. Use search to filter further.