Product Recalls in Delaware

Product recalls affecting Delaware — including food, drugs, consumer products, medical devices, and vehicles distributed to Delaware. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,667 recalls have been distributed to Delaware in the last 12 months.

48,330 total recalls
1,667 in last 12 months

Showing 4604146060 of 48,330 recalls

Medical DeviceNovember 10, 2012· Orthovita, Inc., dBA Stryker Orthobiologics.

Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...

The Issue: There have been a few reported cases of the catheter breaking when removing...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2012· Orthovita, Inc., dBA Stryker Orthobiologics.

Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...

The Issue: There have been a few reported cases of the catheter breaking when removing...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2012· Orthovita, Inc., dBA Stryker Orthobiologics.

Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...

The Issue: There have been a few reported cases of the catheter breaking when removing...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2012· Orthovita, Inc., dBA Stryker Orthobiologics.

Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...

The Issue: There have been a few reported cases of the catheter breaking when removing...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2012· Orthovita, Inc., dBA Stryker Orthobiologics.

Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...

The Issue: There have been a few reported cases of the catheter breaking when removing...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2012· Orthovita, Inc., dBA Stryker Orthobiologics.

Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...

The Issue: There have been a few reported cases of the catheter breaking when removing...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2012· Orthovita, Inc., dBA Stryker Orthobiologics.

Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...

The Issue: There have been a few reported cases of the catheter breaking when removing...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2012· Orthovita, Inc., dBA Stryker Orthobiologics.

Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...

The Issue: There have been a few reported cases of the catheter breaking when removing...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2012· Orthovita, Inc., dBA Stryker Orthobiologics.

Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...

The Issue: There have been a few reported cases of the catheter breaking when removing...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2012· Orthovita, Inc., dBA Stryker Orthobiologics.

Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...

The Issue: There have been a few reported cases of the catheter breaking when removing...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2012· Orthovita, Inc., dBA Stryker Orthobiologics.

Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...

The Issue: There have been a few reported cases of the catheter breaking when removing...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2012· Orthovita, Inc., dBA Stryker Orthobiologics.

Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...

The Issue: There have been a few reported cases of the catheter breaking when removing...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2012· Orthovita, Inc., dBA Stryker Orthobiologics.

Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...

The Issue: There have been a few reported cases of the catheter breaking when removing...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugNovember 9, 2012· Ranbaxy Inc.

Recalled Item: Atorvastatin Calcium Tablets Recalled by Ranbaxy Inc. Due to Presence of...

The Issue: Presence of Particulate Matter: Certain batches of Atorvastatin tablets 10...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugNovember 9, 2012· Ranbaxy Inc.

Recalled Item: Atorvastatin Calcium Tablets Recalled by Ranbaxy Inc. Due to Presence of...

The Issue: Presence of Particulate Matter: Certain batches of Atorvastatin tablets 10...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugNovember 9, 2012· Ranbaxy Inc.

Recalled Item: Atorvastatin Calcium Tablets Recalled by Ranbaxy Inc. Due to Presence of...

The Issue: Presence of Particulate Matter: Certain batches of Atorvastatin tablets 10...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
FoodNovember 9, 2012· Frito Lay, Inc

Recalled Item: Grandma's Peanut Butter Mini Sandwich Creme Cookies Recalled by Frito Lay,...

The Issue: The firm is recalling GRANDMA'S Peanut Butter Sandwich Creme cookies and...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodNovember 9, 2012· Frito Lay, Inc

Recalled Item: Grandma's Peanut Butter Sandwich Creme Cookies Recalled by Frito Lay, Inc...

The Issue: The firm is recalling GRANDMA'S Peanut Butter Sandwich Creme cookies and...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceNovember 9, 2012· Cooper Vision Caribbean Corp.

Recalled Item: AVAIRA (enfilcon A) Soft (Hydrophilic) Daily Wear Toric Contact Lenses...

The Issue: The lenses exceeded the acceptance limit for silicone oil residual.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare became...

The Issue: GE Healthcare became aware of a potential issue associated with the LOGIQ e...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing