Product Recalls in Arkansas

Product recalls affecting Arkansas — including food, drugs, consumer products, medical devices, and vehicles distributed to Arkansas. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,635 recalls have been distributed to Arkansas in the last 12 months.

49,990 total recalls
2,635 in last 12 months

Showing 59415960 of 49,990 recalls

FoodApril 10, 2024· FEEL GOOD FOODS INC

Recalled Item: Cream Cheese Stuffed Plain Mini Bagels Recalled by FEEL GOOD FOODS INC Due...

The Issue: Contains undeclared gluten

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 10, 2024· FEEL GOOD FOODS INC

Recalled Item: Cream Cheese Stuffed Everything Mini Bagels Recalled by FEEL GOOD FOODS INC...

The Issue: Contains undeclared gluten

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 10, 2024· Imprimis NJOF, LLC

Recalled Item: Prednisolone Sodium Phosphate-Moxifloxacin-Bromfenac Sterile Ophthalmic...

The Issue: Subpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 10, 2024· Imprimis NJOF, LLC

Recalled Item: Epinephrine-Lidocaine HCl 0.25 mg/mL and 7.5 mg/mL Preservative-Free...

The Issue: Out of specification for assay

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

Class III — Low RiskOngoing
Refund
Medical DeviceApril 10, 2024· LEICA BIOSYSTEMS NUSSLOCH GMBH

Recalled Item: Leica HistoCore PEGASUS Tissue Processor Recalled by LEICA BIOSYSTEMS...

The Issue: Poorly processed and/or damaged biopsy tissue specimens on the device...

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

Class II — Potential Health HazardOngoing
DrugApril 9, 2024· Second Tokushima Factory, Otsuka Pharmaceutical Co., Ltd.

Recalled Item: Abilify (aripiprazole) Recalled by Second Tokushima Factory, Otsuka...

The Issue: Cross Contamination with Other Products

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

Class III — Low RiskOngoing
Refund
DrugApril 9, 2024· Second Tokushima Factory, Otsuka Pharmaceutical Co., Ltd.

Recalled Item: Abilify (aripiprazole) Recalled by Second Tokushima Factory, Otsuka...

The Issue: Cross Contamination with Other Products

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

Class III — Low RiskOngoing
Refund
DrugApril 9, 2024· Second Tokushima Factory, Otsuka Pharmaceutical Co., Ltd.

Recalled Item: Abilify (aripiprazole) Recalled by Second Tokushima Factory, Otsuka...

The Issue: Cross Contamination with Other Products

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

Class III — Low RiskOngoing
Refund
DrugApril 9, 2024· Second Tokushima Factory, Otsuka Pharmaceutical Co., Ltd.

Recalled Item: Abilify (aripiprazole) Recalled by Second Tokushima Factory, Otsuka...

The Issue: Cross Contamination with Other Products

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

Class III — Low RiskOngoing
Refund
Medical DeviceApril 9, 2024· GE Medical Systems Information Technologies Inc

Recalled Item: GE HealthCare CRITIKON ONE-CUF blood pressure cuffs Recalled by GE Medical...

The Issue: Use of the blood pressure cuffs could result in inaccurate non-invasive...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2024· Sophysa S.A.

Recalled Item: The Sophysa Pressio¿ Ventricular Intracranial Pressure Monitoring Kit...

The Issue: An increase in claims related to leakage of cerebrospinal fluid (CSF) from...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2024· Sophysa S.A.

Recalled Item: The Sophysa Pressio¿ Ventricular Intracranial Pressure Monitoring Kit...

The Issue: An increase in claims related to leakage of cerebrospinal fluid (CSF) from...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2024· QUIDELORTHO

Recalled Item: VITROS Immunodiagnostic Products Free T3 Calibrators-IVD are for use with...

The Issue: Free T3 Calibrators used with T3 Reagent Packs may produce positively biased...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2024· Baxter Healthcare Corporation

Recalled Item: Spectrum IQ Infusion pump Recalled by Baxter Healthcare Corporation Due to...

The Issue: There is a potential for cracks on the mount of the front panel of the device.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2024· QUIDELORTHO

Recalled Item: VITROS Immunodiagnostic Products Free T3 Reagent Pack-IVD is for the...

The Issue: T3 Reagent Packs used with Free T3 Calibrators may produce positively biased...

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

Class II — Potential Health HazardOngoing
DrugApril 8, 2024· Dr. Reddy's Laboratories, Inc.

Recalled Item: Sapropterin Dihydrochloride Powder for Oral Solution 100mg Recalled by Dr....

The Issue: Sub-potent Drug; powder discoloration associated with decreased potency

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 8, 2024· Dr. Reddy's Laboratories, Inc.

Recalled Item: Javygtor (sapropterin dihydrochloride) Powder for Oral Solution 100mg...

The Issue: Sub-potent Drug; powder discoloration associated with decreased potency

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceApril 8, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline procedure kits labeled as: 1) NEPHROLOGY PACK Recalled by MEDLINE...

The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 8, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline procedure kits labeled as: 1) WMC HYBRID OR PACK PART 1 Recalled by...

The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 8, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline procedure kits labeled as: 1) CONTINUOUS BLOCK Recalled by MEDLINE...

The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...

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

Class I — Serious Health HazardOngoing