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 2992129940 of 53,623 recalls

DrugSeptember 1, 2017· Pharmedium Services, LLC

Recalled Item: Oxytocin 10 units added to 1000 mL Lactated Ringer's Injection Recalled by...

The Issue: Subpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 1, 2017· Respire Medical

Recalled Item: Respire Pink+ Hard/Soft Oral Sleep Apnea Device Recalled by Respire Medical...

The Issue: Potential for device breakage during use

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 1, 2017· Respire Medical

Recalled Item: Respire Pink+ Hard Oral Sleep Apnea Device Recalled by Respire Medical Due...

The Issue: Potential for device breakage during use

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 1, 2017· Respire Medical

Recalled Item: Respire Pink Series EF+ Oral Sleep Apnea Device. Recalled by Respire Medical...

The Issue: Potential for device breakage during use

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 1, 2017· Respire Medical

Recalled Item: Respire Pink H/S Oral Sleep Apnea Device Recalled by Respire Medical Due to...

The Issue: Potential for device breakage during use

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 1, 2017· Respire Medical

Recalled Item: Respire Pink H/S Oral Sleep Apnea Device Recalled by Respire Medical Due to...

The Issue: Potential for device breakage during use

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 1, 2017· Aesculap Implant Systems LLC

Recalled Item: The ELAN 4 Air System is intended for high speed cutting Recalled by...

The Issue: The ELAN 4 Air System was released to the market place prior to an...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 1, 2017· Permobil, Ab

Recalled Item: Electric Wheelchair bases: a) C300 b) C350 c) C400 d) C500 Recalled by...

The Issue: There is a potential failure of the top plate assembly, which is the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 1, 2017· Aaren Scientific Inc.

Recalled Item: AERO IOL Injection System containing 10 Z28 Cartridges per box Recalled by...

The Issue: The recommended storage temperature on the label is incorrect.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 1, 2017· Baxter Healthcare Corp

Recalled Item: Baxter Amia Automated Peritoneal Dialysis Set with Cassette Recalled by...

The Issue: The firm received increased customer complaints for Missing Red Line,...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 1, 2017· Permobil, Ab

Recalled Item: Electric Wheelchairs: a) C300 CORPUS II b) C350 CORPUS II Recalled by...

The Issue: There is a potential failure of the top plate assembly, which is the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 1, 2017· Elekta Inc

Recalled Item: Elekta ERGO++ Product Usage: ERGO is often used for stereotactic treatments....

The Issue: Incorrect DICOM mapping of the exported collimator or couch angles from...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2017· Orthoscan, Inc.

Recalled Item: Mobile Mini C-arm system Part # 1000-0001. Intended to provide Recalled by...

The Issue: OrthoScan Inc. discovered during investigation of a non-standard work flow a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2017· Orthoscan, Inc.

Recalled Item: Mobile Mini C-arm system Part # 1000-0004. Intended to provide Recalled by...

The Issue: OrthoScan Inc. discovered during investigation of a non-standard work flow a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2017· Orthoscan, Inc.

Recalled Item: Mobile Mini C-arm system Part # 1000-0004-FD. Intended to provide Recalled...

The Issue: OrthoScan Inc. discovered during investigation of a non-standard work flow a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2017· Exactech, Inc.

Recalled Item: Equinoxe Cage Recalled by Exactech, Inc. Due to Mislabeling

The Issue: Potentially mislabeled.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2017· Orthoscan, Inc.

Recalled Item: Mobile Mini C-arm system Part # 1000-0005. Intended to provide Recalled by...

The Issue: OrthoScan Inc. discovered during investigation of a non-standard work flow a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2017· Exactech, Inc.

Recalled Item: Equinoxe Cage Recalled by Exactech, Inc. Due to Mislabeling

The Issue: Potentially mislabeled.

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

Class II — Potential Health HazardOngoing
FoodAugust 31, 2017· Reese Pharmaceutical Company

Recalled Item: Berry Flavor Immune Support Dietary Supplement Effervescent Tablets 10...

The Issue: The label does not list "Sodium" in the ingredient statement.

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 31, 2017· Reese Pharmaceutical Company

Recalled Item: Orange Flavor Immune Support Dietary Supplement Effervescent Tablets 10...

The Issue: The label does not list "Sodium" in the ingredient statement.

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

Class II — Potential Health HazardOngoing
Refund