Product Recalls in Georgia

Product recalls affecting Georgia — including food, drugs, consumer products, medical devices, and vehicles distributed to Georgia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,643 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
2,643 in last 12 months

Showing 2970129720 of 53,623 recalls

DrugOctober 10, 2017· Banner Pharmacy Services, LLC

Recalled Item: VANCOmycin 1.5 grams added to 0.9% Sodium Chloride 500 mL bag Recalled by...

The Issue: Lack of Assurance of Sterility.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 10, 2017· Implant Direct Sybron Manufacturing, LLC

Recalled Item: ImplantDirect Legacy(TM) 3 Implant Recalled by Implant Direct Sybron...

The Issue: One reported complaint and discovered that the outer vial was out of round...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2017· Karl Storz Endoscopy

Recalled Item: STORZ High Flow Insufflation Tubing (with filter) Recalled by Karl Storz...

The Issue: The label outside the cardboard box is labeled correctly but the pouches...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2017· Medline Industries Inc

Recalled Item: MEDLINE DOUBLE SWIVEL CLOSED SUCTION CATHETER Recalled by Medline Industries...

The Issue: Products labeled as sterile were distributed prior to sterilization

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2017· Medline Industries Inc

Recalled Item: MEDLINE PEDI ELBOW CLOSED SUCTION CATHETER Recalled by Medline Industries...

The Issue: Products labeled as sterile were distributed prior to sterilization

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

Class II — Potential Health HazardOngoing
FoodOctober 10, 2017· La Terra Fina, Inc.

Recalled Item: La Terra Fina Spinach Artichoke & Parmesan Dip & Spread Recalled by La Terra...

The Issue: Undeclared allergen; egg.

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 9, 2017· General Mills, Inc

Recalled Item: Cascadian Farm Organic Cinnamon Raisin Granola Recalled by General Mills,...

The Issue: General Mills is recalling 2 production runs of Cascadian Farm Organic...

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 6, 2017· Bel Brands USA

Recalled Item: Merkts Port Wine Cheese Spread Recalled by Bel Brands USA Due to Bel Brands...

The Issue: Bel Brands USA is recalling Merkts Port Wine Cheese Spread after being...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 6, 2017· Whole Foods Market Brand 365, Llc

Recalled Item: 365 Organic Raisin Bran Flakes 15 oz. packaged in plastic bag Recalled by...

The Issue: Undeclared (peanut) allergen: 365 Organic Peanut Butter and Cocoa Balls were...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceOctober 6, 2017· Allen Medical Systems

Recalled Item: Allen Medical Bow Frame Model A-70800. Surgical platform used to Recalled by...

The Issue: The base of the frame has the potential to crack when the patient is...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2017· Allen Medical Systems

Recalled Item: Radiolucent Surgery Spine Frame (F70801). Surgical platform used to position...

The Issue: The base of the frame has the potential to crack when the patient is...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2017· CooperSurgical, Inc.

Recalled Item: Cooper Surgical 2 MHZ Waterproof OB Probe Product The CooperSurgical...

The Issue: The 2MHZ prove was...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2017· Halyard Health, Inc

Recalled Item: Halyard Closed Suction System for Adults Recalled by Halyard Health, Inc Due...

The Issue: Received recall notification from Smiths Medical that lots of 15ml Saline...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2017· Halyard Health, Inc

Recalled Item: Halyard Closed Suction System for Adults Recalled by Halyard Health, Inc Due...

The Issue: Received recall notification from Smiths Medical that lots of 15ml Saline...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2017· Halyard Health, Inc

Recalled Item: Halyard Closed Suction System for Adults Recalled by Halyard Health, Inc Due...

The Issue: Received recall notification from Smiths Medical that lots of 15ml Saline...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2017· Halyard Health, Inc

Recalled Item: Halyard Turbo-Cleaning Closed Suction System for Adults Recalled by Halyard...

The Issue: Received recall notification from Smiths Medical that lots of 15ml Saline...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2017· Halyard Health, Inc

Recalled Item: NOVAPLUS* Endotracheal WET PAK* Closed Suction System for Adults with...

The Issue: Received recall notification from Smiths Medical that lots of 15ml Saline...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2017· Halyard Health, Inc

Recalled Item: Halyard Closed Suction System for Adults with BALLARD Technology WET...

The Issue: Received recall notification from Smiths Medical that lots of 15ml Saline...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2017· Halyard Health, Inc

Recalled Item: Halyard Closed Suction System for Adults Recalled by Halyard Health, Inc Due...

The Issue: Received recall notification from Smiths Medical that lots of 15ml Saline...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2017· Halyard Health, Inc

Recalled Item: Halyard Turbo-Cleaning Closed Suction System for Adults Recalled by Halyard...

The Issue: Received recall notification from Smiths Medical that lots of 15ml Saline...

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

Class II — Potential Health HazardOngoing