2017-01-22 04:30:24 UPDATED: (M8.0) BOUGAINVILLE REGION, PAPUA NEW GUINEA -6.3 155.1 (442af)

M8.0 - BOUGAINVILLE REGION, PAPUA NEW GUINEA

Preliminary Earthquake Report

Magnitude	8.0
Date-Time	22 Jan 2017 04:30:25 UTC 22 Jan 2017 15:30:25 near epicenter 21 Jan 2017 18:30:25 standard time in your timezone
Location	6.267S 155.119E
Depth	153 km
Distances	40 km (24 mi) W of Panguna, Papua New Guinea 46 km (28 mi) W of Arawa, Papua New Guinea 380 km (235 mi) SE of Kokopo, Papua New Guinea 556 km (344 mi) E of Kimbe, Papua New Guinea 637 km (394 mi) WNW of Honiara, Solomon Islands
Location Uncertainty	Horizontal: 7.9 km; Vertical 5.7 km
Parameters	Nph = 103; Dmin = 399.5 km; Rmss = 1.07 seconds; Gp = 29° Version =
Event ID	us 10007uph

For updates, maps, and technical information
see: Event Page or USGS Earthquake Hazards Program
National Earthquake Information Center
U.S. Geological Survey


Disclaimer

This email was sent to filter@clubhouseb.com

You requested mail for events between -90.0/90.0 latitude and 180.0/-180.0 longitude (Default World)
for M6.0 between 09:00 and 21:00 and M6.5 other times.
Your account has aftershock exclusion turned on. This event fell into the 'PT16352050' exclusion region, but was large enough to trigger notification.
To change your parameters, go to: https://sslearthquake.usgs.gov/ens
To unsubscribe, send a one-line reply to this message with: STOP filter@clubhouseb.com

2017-01-19 23:04:20 UPDATED: (M6.8) SOLOMON ISLANDS -10.4 161.3 (442af)

M6.8 - SOLOMON ISLANDS

Preliminary Earthquake Report

Magnitude	6.8
Date-Time	19 Jan 2017 23:04:21 UTC 20 Jan 2017 10:04:21 near epicenter 19 Jan 2017 13:04:21 standard time in your timezone
Location	10.351S 161.280E
Depth	33 km
Distances	71 km (44 mi) W of Kirakira, Solomon Islands 177 km (109 mi) SE of Honiara, Solomon Islands 780 km (483 mi) SE of Arawa, Papua New Guinea 858 km (531 mi) NW of Luganville, Vanuatu 1115 km (691 mi) NW of Port-Vila, Vanuatu
Location Uncertainty	Horizontal: 8.0 km; Vertical 4.6 km
Parameters	Nph = 133; Dmin = 177.3 km; Rmss = 1.20 seconds; Gp = 20° Version =
Event ID	us 10007u7n

For updates, maps, and technical information
see: Event Page or USGS Earthquake Hazards Program
National Earthquake Information Center
U.S. Geological Survey


Disclaimer

This email was sent to filter@clubhouseb.com

You requested mail for events between -90.0/90.0 latitude and 180.0/-180.0 longitude (Default World)
for M6.0 between 09:00 and 21:00 and M6.5 other times.
Your account has aftershock exclusion turned on. This event fell into the 'AT00ohvnon' exclusion region, but was large enough to trigger notification.
To change your parameters, go to: https://sslearthquake.usgs.gov/ens
To unsubscribe, send a one-line reply to this message with: STOP filter@clubhouseb.com

D.F. Stauffer Biscuit Co., Inc. Issues Allergy Alert and Voluntary Recall on One Specific Best By Date Of 32oz Original Animal Crackers Due to Undeclared Milk Ingredient

You are subscribed to Recalls, Market Withdrawals and Safety Alerts for U.S. Food & Drug Administration (FDA).

This information has recently been updated and is now available.

 

 

D.F. Stauffer Biscuit Co., Inc. Issues Allergy Alert and Voluntary Recall on One Specific Best By Date Of 32oz Original Animal Crackers Due to Undeclared Milk Ingredient

01/18/2017 04:02 PM EST

anuary 18, 2017 – D. F. Stauffer Biscuit Co., Inc. is voluntarily recalling one specific best by date of 32 oz. Original Animal Cracker because they may be packaged with other cookies that contain milk powder. People who are allergic to milk run the risk of serious or life-threatening allergic reactions if they consume this product.

For detailed information pertaining to this Recalls, Market Withdrawals and Safety Alerts message, please click the link at the beginning of this bulletin.

---

Manage your FDA Subscriptions:

• Update your preferences or unsubscribe
• Questions about this service? Please visit subscriberhelp.govdelivery.com
• Other inquiries? webmail@oc.fda.gov

---

This email was sent to filter@clubhouseb.com using GovDelivery, on behalf of: U.S. Food & Drug Administration (FDA) · 10903 New Hampshire Ave · Silver Spring, MD 20993 · 1-888-INFO-FDA (1-888-463-6332)

Blue Ridge Beef Recalls Product Because of Possible Health Risk

You are subscribed to Recalls, Market Withdrawals and Safety Alerts for U.S. Food & Drug Administration (FDA).

This information has recently been updated and is now available.

 

 

Blue Ridge Beef Recalls Product Because of Possible Health Risk

01/17/2017 10:42 AM EST

Blue Ridge Beef is voluntarily recalling one (1) of its frozen products due to their potential to be contaminated with Listeria monocytogenes. Listeria can affect animals eating the product. There is a risk to humans from handling contaminated pet products, especially if they have not thoroughly washed their hands after having contact with the products or any surface exposed to these products.

For detailed information pertaining to this Recalls, Market Withdrawals and Safety Alerts message, please click the link at the beginning of this bulletin.

---

Manage your FDA Subscriptions:

• Update your preferences or unsubscribe
• Questions about this service? Please visit subscriberhelp.govdelivery.com
• Other inquiries? webmail@oc.fda.gov

---

This email was sent to filter@clubhouseb.com using GovDelivery, on behalf of: U.S. Food & Drug Administration (FDA) · 10903 New Hampshire Ave · Silver Spring, MD 20993 · 1-888-INFO-FDA (1-888-463-6332)

Grange Co-Op Recalls Rogue All Purpose Rabbit Pellets For High Vitamin D Health Risk

You are subscribed to Recalls, Market Withdrawals and Safety Alerts for U.S. Food & Drug Administration (FDA).

This information has recently been updated and is now available.

 

 

Grange Co-Op Recalls Rogue All Purpose Rabbit Pellets For High Vitamin D Health Risk

01/14/2017 08:08 AM EST

Grange Co-op is initiating a recall of Rogue All Purpose Rabbit Pellets in 25# (25RP) 50# (50RP), 1,500# Tote (RP) no lot codes- purchased between March 1, 2016 and January 12, 2017 in Southern Oregon / Northern California from any Grange Co-op Retail Store or Wholesale Dealer. The recall is being initiated because samples tested by the Oregon Department of Agriculture discovered these products may contain higher than acceptable levels of vitamin D.

For detailed information pertaining to this Recalls, Market Withdrawals and Safety Alerts message, please click the link at the beginning of this bulletin.

---

Manage your FDA Subscriptions:

• Update your preferences or unsubscribe
• Questions about this service? Please visit subscriberhelp.govdelivery.com
• Other inquiries? webmail@oc.fda.gov

---

This email was sent to filter@clubhouseb.com using GovDelivery, on behalf of: U.S. Food & Drug Administration (FDA) · 10903 New Hampshire Ave · Silver Spring, MD 20993 · 1-888-INFO-FDA (1-888-463-6332)

The Pictsweet Company Announces Voluntary Recall of Pictsweet Farms 12oz Breaded Okra due to Risk of Glass Contamination

You are subscribed to Recalls, Market Withdrawals and Safety Alerts for U.S. Food & Drug Administration (FDA).

This information has recently been updated and is now available.

 

 

The Pictsweet Company Announces Voluntary Recall of Pictsweet Farms 12oz Breaded Okra due to Risk of Glass Contamination

01/14/2017 04:53 PM EST

The Pictsweet Company is voluntarily recalling select packages of Pictsweet Farms 12 ounce Breaded Okra after the company learned that some packages may contain glass fragments, which could cause injury if ingested. There has been one minor injury reported in connection with this issue.

For detailed information pertaining to this Recalls, Market Withdrawals and Safety Alerts message, please click the link at the beginning of this bulletin.

---

Manage your FDA Subscriptions:

• Update your preferences or unsubscribe
• Questions about this service? Please visit subscriberhelp.govdelivery.com
• Other inquiries? webmail@oc.fda.gov

---

This email was sent to filter@clubhouseb.com using GovDelivery, on behalf of: U.S. Food & Drug Administration (FDA) · 10903 New Hampshire Ave · Silver Spring, MD 20993 · 1-888-INFO-FDA (1-888-463-6332)

Physio-Control Launches Voluntary Field Action for LIFEPAK 1000 Defibrillator

You are subscribed to Recalls, Market Withdrawals and Safety Alerts for U.S. Food & Drug Administration (FDA).

This information has recently been updated and is now available.

 

 

Physio-Control Launches Voluntary Field Action for LIFEPAK 1000 Defibrillator

01/13/2017 06:11 PM EST

Physio-Control announced today that the company is launching a voluntary field action for the LIFEPAK 1000 defibrillator due to reported instances where the device has shut down unexpectedly during patient treatment.

For detailed information pertaining to this Recalls, Market Withdrawals and Safety Alerts message, please click the link at the beginning of this bulletin.

---

Manage your FDA Subscriptions:

• Update your preferences or unsubscribe
• Questions about this service? Please visit subscriberhelp.govdelivery.com
• Other inquiries? webmail@oc.fda.gov

---

This email was sent to filter@clubhouseb.com using GovDelivery, on behalf of: U.S. Food & Drug Administration (FDA) · 10903 New Hampshire Ave · Silver Spring, MD 20993 · 1-888-INFO-FDA (1-888-463-6332)