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. 2,819 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
2,819 in last 12 months

Showing 89618980 of 53,623 recalls

Medical DeviceJuly 7, 2023· Alphatec Spine, Inc.

Recalled Item: LIF AMP Recalled by Alphatec Spine, Inc. Due to Awl instrument adjustable...

The Issue: Awl instrument adjustable drill button assembly assembled in the incorrect...

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

Class II — Potential Health HazardOngoing
FoodJuly 6, 2023· Betty Lou's Inc

Recalled Item: Betty Lou's Paleo Java Nuts About Energy Balls with Cacao Recalled by Betty...

The Issue: Undeclared sesame. Paleo Java Nuts About Energy Balls with Cacao, Coffee &...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJuly 6, 2023· Aquila Corporation

Recalled Item: APK2 Pressure-Sensing Wheelchair Cushions Recalled by Aquila Corporation Due...

The Issue: Defective battery pack in wheelchair cushions can overheat resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2023· Aquila Corporation

Recalled Item: SofTech Pressure-Sensing Wheelchair Cushions Recalled by Aquila Corporation...

The Issue: Defective battery pack in wheelchair cushions can overheat resulting in...

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

Class II — Potential Health HazardOngoing
DrugJuly 5, 2023· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Loteprednol Etabonate Ophthalmic Suspension Recalled by SUN PHARMACEUTICAL...

The Issue: Superpotent Drug: Out of Specification (OOS) results observed for unit dose...

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

Class III — Low RiskOngoing
Refund
DrugJuly 5, 2023· Teva Pharmaceuticals USA Inc

Recalled Item: Sunitinib Malate Capsules Recalled by Teva Pharmaceuticals USA Inc Due to...

The Issue: Failed Moisture Limits: Water (moisture) content above the approved product...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 5, 2023· B. Braun Medical Inc.

Recalled Item: 0.9% Sodium Chloride Injection USP Recalled by B. Braun Medical Inc. Due to...

The Issue: Lack of assurance of sterility: bags have the potential to leak.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 3, 2023· Accord Healthcare, Inc.

Recalled Item: Bivalirudin for Injection 250 mg Recalled by Accord Healthcare, Inc. Due to...

The Issue: Presence of Particulate Matter: Particulate matter identified as fiber.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 3, 2023· Accord Healthcare, Inc.

Recalled Item: Atropine Sulfate Injection Recalled by Accord Healthcare, Inc. Due to...

The Issue: Presence of Particulate Matter: Particulate matter identified as fiber.

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 3, 2023· US Waffle Company, INC.

Recalled Item: Vans gluten free ORIGINAL WAFFLES Recalled by US Waffle Company, INC. Due to...

The Issue: The firm was notified, by a consumer, that the product contains undeclared...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJuly 3, 2023· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: LINK MP Monoblock Hip Stem Recalled by Waldemar Link GmbH & Co. KG (Mfg...

The Issue: Increased force may be required to remove the LINK MP Monoblock trial hip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2023· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: LINK MP Monoblock Hip Stem Recalled by Waldemar Link GmbH & Co. KG (Mfg...

The Issue: Increased force may be required to remove the LINK MP Monoblock trial hip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2023· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: LINK MP Monoblock Hip Stem Recalled by Waldemar Link GmbH & Co. KG (Mfg...

The Issue: Increased force may be required to remove the LINK MP Monoblock trial hip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Total Hip Kit Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to The...

The Issue: The prep solution included in the Total Hip Kit expires prior to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2023· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: LINK MP Monoblock Hip Stem Recalled by Waldemar Link GmbH & Co. KG (Mfg...

The Issue: Increased force may be required to remove the LINK MP Monoblock trial hip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2023· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: LINK MP Monoblock Hip Stem Recalled by Waldemar Link GmbH & Co. KG (Mfg...

The Issue: Increased force may be required to remove the LINK MP Monoblock trial hip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2023· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: LINK MP Monoblock Hip Stem Recalled by Waldemar Link GmbH & Co. KG (Mfg...

The Issue: Increased force may be required to remove the LINK MP Monoblock trial hip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2023· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: LINK MP Monoblock Hip Stem Recalled by Waldemar Link GmbH & Co. KG (Mfg...

The Issue: Increased force may be required to remove the LINK MP Monoblock trial hip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2023· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: LINK MP Monoblock Hip Stem Recalled by Waldemar Link GmbH & Co. KG (Mfg...

The Issue: Increased force may be required to remove the LINK MP Monoblock trial hip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2023· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: LINK MP Monoblock Hip Stem Recalled by Waldemar Link GmbH & Co. KG (Mfg...

The Issue: Increased force may be required to remove the LINK MP Monoblock trial hip...

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

Class II — Potential Health HazardOngoing