Georgia recalls
3,596 federal recalls affecting Georgia in the last 12 months - 234 Georgia-specific plus 3,362 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 2025-12-24FDA-DrugPreferred PharmaceuticalsClass IINationwideStop using Preferred Pharmaceuticals ondansetron ODT
Preferred Pharmaceuticals is recalling ondansetron ODT 4mg tablets because the blister pack containers are not fully sealed, which can cause tablets to fall out. The manufacturer Glenmark Pharmaceuticals notified Preferred Pharmaceuticals of the sealing defect. This affects specific lot numbers distributed nationwide.
- 2025-12-24FDA-DrugSomerset TherapeuticsClass IIINationwideStop using Somerset Therapeutics cisatracurium besylate
Somerset Therapeutics is recalling cisatracurium besylate injection (a muscle relaxant used during surgery) because stability testing found the drug strength fell below the required standard. Lot A250043 with expiration date 06/30/2026 is affected. The company has not reported any injuries.
- 2025-12-24FDA-DrugSomerset TherapeuticsClass IIINationwideStop using Somerset cisatracurium besylate injection
Somerset Therapeutics is recalling cisatracurium besylate injection (200mg/20mL vials, Lot #A250020, expiration 06/30/2026) because stability testing found the drug's strength fell below required standards. This means the medication may not work as intended during medical procedures.
- 2025-12-24FDA-DrugSomerset TherapeuticsClass IIINationwideCheck cisatracurium besylate vials for affected lots
Somerset Therapeutics is recalling specific lots of cisatracurium besylate injection because testing found the drug contains less active ingredient than labeled. The affected vials may not work as intended during medical procedures. No injuries have been reported.
- 2025-12-24FDA-DrugGolden State Medical SupplyClass IINationwideStop using Golden State Medical Supply baclofen
Golden State Medical Supply's baclofen 10 mg tablets in 1,000-count bottles (Lot GS065762) may contain foreign tablets or capsules mixed in. This affects 2,472 bottles distributed nationwide. No injuries have been reported.
- 2025-12-24FDA-DrugNovocolClass IINationwideStop using OraVerse injection cartridges
OraVerse (phentolamine mesylate) injection cartridges in one lot have been found with cracks or breaks in the container. Affected cartons contain 10 cartridges each and were distributed nationwide. No injuries have been reported.
- 2025-12-24FDA-DrugNovocolClass IINationwideStop using Novocol Carbocaine 3% injection
Novocol Pharmaceutical is recalling one lot of Carbocaine 3% mepivacaine injection because some cartridges in affected cartons are cracked or broken. Cracked containers can allow contamination or leakage of the medication. No injuries have been reported.
- 2025-12-24FDA-DrugNovocolClass IINationwideStop using Novocol Mepivacaine HCI injection
Benco Dental is recalling Mepivacaine HCI 3% injection cartridges (lot D05159H, expires 07-31-2027) because some cartridges may be cracked or broken. A defective container could allow the medication to leak or become contaminated. No injuries have been reported.
- 2025-12-24FDA-DrugNovocolClass IINationwideStop using Novocol Mepivacaine injection cartridges
Novocol Pharmaceutical's Mepivacaine HCI 3% injection cartridges may have cracked or broken containers. This defect affects one lot (D05159G) distributed nationwide. The cracked cartridges could compromise the integrity of the medication.
- 2025-12-24FDA-DrugNovocolClass IINationwideStop using recalled Polocaine dental anesthetic
Novocol Polocaine 3% dental anesthetic cartridges in one specific lot may have cracked or broken containers. This defect could compromise the sterility and safety of the medication. No injuries have been reported.
- 2025-12-24FDA-DrugNovocolClass IINationwideStop using Novocol lidocaine-epinephrine cartridges
Novocol Pharmaceutical's lidocaine HCI 2% and epinephrine injection cartridges (50-count boxes) may have cracks or breaks in the containers. This defect could affect the sterility and safety of the medication. The affected lot D05362A expires July 31, 2027.
- 2025-12-24FDA-DrugNovocolClass IINationwideStop using Novocol Xylocaine Dental cartridges
Novocol Pharmaceutical issued a recall of 2% Xylocaine Dental with Epinephrine 1:100,000 injection cartridges due to defective containers—some cartridges are cracked or broken. This affects lot D05337B (expires 06-30-2027). The problem was discovered during quality control; no injuries have been reported.
- 2025-12-19USDAClass INationwideThrow away Olympia Provisions holiday kielbasa
Olympia Provisions is recalling about 1,930 pounds of ready-to-eat holiday kielbasa sausage because metal fragments may be in the product. The sausages were produced on October 14, 2025, and sold in 16-ounce packages with a "best if used by" date of 02/19/26. No injuries have been reported so far.
- 2025-12-19USDAClass IDon't eat Lorraine Quiche with pork
Maître Saladier Inc. recalled about 6,000 pounds of Lorraine Quiche products with pork that were shipped to the U.S. without proper import inspection. The quiches were produced in April 2025 and lack a USDA inspection mark. No illnesses have been reported, but the products may still be in home freezers.
- 2025-12-18CPSCAngeer-USNationwideStop using Meaicezli Play Purse Sets immediately
Meaicezli Play Purse Sets contain toy cell phones and writing tablets with button or coin cell batteries that children can easily remove and swallow. Swallowing these batteries can cause serious internal injuries, chemical burns, and death.
- 2025-12-18CPSCBlue Wave ProductsNationwideStop using your Blue Wave pool
Blue Wave above-ground pools 48 inches and taller have a compression strap around the outside of the pool legs that can act as a foothold, allowing children to climb into the pool unsupervised. This creates a serious drowning risk. The strap can provide access to the pool even if you remove the ladder.
- 2025-12-18CPSCSereneLifeNationwideStop using SereneLife Home above-ground pools
- 2025-12-18CPSCJuyuanNationwideStop using ANNQUAN power strips immediately
ANNQUAN power strips (models EX-D112-05 and EX-D106-25) lack proper safety protection and can overheat and catch fire if overloaded. Seven units have blown fuses. The fire risk can cause serious injury or death from burns and smoke.
- 2025-12-18CPSCJOKOSISNationwideStop using JOKOSIS bed rails immediately
JOKOSIS bed rails (model HC0262) can trap users between the rail and mattress, creating a serious risk of entrapment and asphyxiation. The rails also lack required warning labels. About 12,000 units were sold on Amazon between August and November 2025.
- 2025-12-18CPSCChangzhou Municipal Sea Metal ProductsNationwideStop using KKL Fabric 9-Drawer Dressers
KKL Fabric 9-Drawer Dressers can tip over and trap children if not anchored securely to the wall. The dressers do not meet federal safety standards for clothing storage units. About 4,740 units were sold on Amazon between September 2023 and November 2025.
- 2025-12-18CPSCFeel The BeardNationwideStop using Feel The Beard beard growth serum
Feel The Beard Beard Growth Oil contains minoxidil, a medication that must be in child-resistant packaging by law. The bottles do not have child-resistant caps, which means young children could open them and swallow the contents, causing serious injury or death. The product was sold online from April through September 2025.
- 2025-12-18CPSCMiramarLabNationwideSecure Mamisan Ointment away from children immediately
Mamisan Pain Relieving Topical Ointment contains lidocaine but does not have child-resistant packaging as required by law. Young children could open the jar and swallow the contents, causing serious injury or death. The recalled product is in a 3.52 ounce orange plastic jar with a white lid and UPC code 860006498115.
- 2025-12-18CPSCShenliNationwideStop using 17 Stories 18-drawer dressers
These 18-drawer dressers can tip over and trap children if not anchored to the wall. The dressers have a metal frame, wooden top, and fabric drawers, and were sold in black, brown, and gray. They fail to meet mandatory safety standards for furniture stability.
- 2025-12-18CPSCCurrey &NationwideContact Currey & Company about your Electra Chandelier
Currey & Company Electra Chandeliers have a defective ceiling connection that may not be threaded properly. This can cause the heavy fixture to fall unexpectedly. Two fixtures have already fallen; one caused property damage.
- 2025-12-18CPSCTopHomerUSNationwideStop using TopHomer pool drain covers
TopHomer 8-inch pool drain covers do not meet federal safety standards and can trap swimmers or bathers, creating a drowning risk. The covers were sold on Amazon from August 2024 through October 2025. No injuries have been reported, but the hazard is serious.
- 2025-12-18CPSCFurnulemNationwideStop using Furnulem 8-Drawer Dressers
Furnulem 8-Drawer Dressers can tip over and trap children if not anchored to the wall. These dressers were sold on Amazon from September 2023 through November 2025. The dressers fail to meet federal safety standards for furniture stability.
- 2025-12-18CPSCPedegoNationwideStop using Pedego Fat Tire Trike immediately
Pedego electric tricycles can develop hairline fractures in the frame near a weld, causing the tubes to separate. This poses a risk of falling off the trike and being cut. The company has received 16 reports of frame breakage, including one injury.
- 2025-12-18CPSCPacific CycleNationwideStop using Schwinn Ovation bike child carrier
The buckles that secure the restraint straps on this rear-mounted bike carrier can release during use, which could cause a child to fall. Pacific Cycle has received one report of buckle failure, though no injuries have been reported yet.
- 2025-12-18CPSCAmp FitNationwideStop using Amp Fit MP2 fitness machine
The arm on Amp Fit's MP2 Smart Fitness Machine can swing unexpectedly because the locking mechanism does not hold securely. The company has received 10 reports of injuries, including lacerations to the head and bruising to the shoulder and other areas.
- 2025-12-17FDA-DeviceStrykerClass IINationwideDo not use Stryker Arise mattress with MV3 bed
Stryker recalled certain Arise 1000EX mattresses because some were sold near MV3 beds, raising concern they might be used together. The mattress and bed have not been tested together and are not designed to work as a pair. Using them together is not recommended by Stryker.
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