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. 1,053 recalls have been distributed to Arkansas in the last 12 months.

49,990 total recalls
1,053 in last 12 months

Showing 15041–15060 of 49,990 recalls

DrugJune 25, 2021· Fresenius Kabi USA LLC

Recalled Item: Xylocaine-MPF with Epinephrine 1:200 Recalled by Fresenius Kabi USA LLC Due...

The Issue: Low out of specification results for epinephrine assay.

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 25, 2021· Dole Fresh Fruit Company

Recalled Item: Dole Fresh Picked-Emballes frais Blueberries/Bleuets: Packed in clear...

The Issue: Canadian Food Inspection Agency tested blueberries and found Cyclospora...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 24, 2021· Avanti Frozen Foods

Recalled Item: Cooked Recalled by Avanti Frozen Foods Due to Potential Salmonella Contamination

The Issue: Potential contamination with Salmonella in frozen cooked shrimp

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 24, 2021· Biomerieux Inc

Recalled Item: ETEST IMIPENEM RELEBACTAM. in vitro diagnostic Recalled by Biomerieux Inc...

The Issue: Major errors (Resistant result instead of Susceptible result) were observed...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2021· Roche Diagnostics Operations, Inc.

Recalled Item: cobas infinity central lab running software version 3.01.03 through 3.02.08...

The Issue: Under specific circumstances created by the user, the cobas e flow test...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2021· CardioQuip, LLC

Recalled Item: CardioQuip Recalled by CardioQuip, LLC Due to There is the potential...

The Issue: There is the potential bacterial including Nontuberculous mycobacterial...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2021· Bard Peripheral Vascular Inc

Recalled Item: TJM6008 Jamshidi" Crown Bone Marrow Biopsy/Aspiration Needle with Marrow...

The Issue: Due to complaints received regarding incomplete/open packaging seals...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2021· Covidien Llc

Recalled Item: Covidien Sonicision Reusable Generator-converts electrical power from the...

The Issue: Potential for a manufacturing assembly error-may result in a non-functional...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2021· Bard Peripheral Vascular Inc

Recalled Item: TIN3018 Illinois Bone Marrow Aspiration/Intraosseous Infusion Needle 18G x...

The Issue: Due to complaints received regarding incomplete/open packaging seals...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2021· Beckman Coulter, Inc.

Recalled Item: Kaluza C Flow Cytometry Software Versions: 1.0* Recalled by Beckman Coulter,...

The Issue: Software anomalies that may lead to the generation of erroneous results.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2021· Bard Peripheral Vascular Inc

Recalled Item: EJM4011 Jamshidi Evolve" Bone Marrow Biopsy/Aspiration Needle with Specimen...

The Issue: Due to complaints received regarding incomplete/open packaging seals...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2021· BioMerieux SA

Recalled Item: MYLA software. Used to manage microbiology test workflow from the Recalled...

The Issue: Software anomaly - Under certain conditions, unwanted alterations to results...

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

Class II — Potential Health HazardOngoing
FoodJune 22, 2021· Del Monte Foods, Inc

Recalled Item: Del Monte Fresh Cut Golden Sweet Whole Kernel Corn Recalled by Del Monte...

The Issue: Firm discovered that some containers exhibited post-process spoilage during...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 22, 2021· HOYU(US) LOGISTICS INC

Recalled Item: QiYu Hand Sanitizer (ethyl alcohol 75% (v/v)) Recalled by HOYU(US) LOGISTICS...

The Issue: Subpotent

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 22, 2021· Teligent Pharma, Inc.

Recalled Item: Erythromycin Topical Solution USP Recalled by Teligent Pharma, Inc. Due to...

The Issue: Failed Impurities/Degradation Specifications

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

Class III — Low RiskOngoing
Refund
DrugJune 22, 2021· Teligent Pharma, Inc.

Recalled Item: Erythromycin Topical Gel Recalled by Teligent Pharma, Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications

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

Class III — Low RiskOngoing
Refund
DrugJune 21, 2021· Prairie Wolf Spirits

Recalled Item: Prairie Wolf Distillery Alcohol Antiseptic 80% Recalled by Prairie Wolf...

The Issue: Hand sanitizer packaged in bottles that resemble beverage containers.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJune 21, 2021· Delta Med SpA

Recalled Item: NEO DELTA Self Safe T Recalled by Delta Med SpA Due to Problems related to...

The Issue: Problems related to the sterilization of the medical devices; possible...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2021· Delta Med SpA

Recalled Item: NEO DELTA SELFSAFE PUR T Recalled by Delta Med SpA Due to Problems related...

The Issue: Problems related to the sterilization of the medical devices; possible...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2021· Delta Med SpA

Recalled Item: WOLF-PAK Self Safe Safety IV Catheter: a) b) Recalled by Delta Med SpA Due...

The Issue: Problems related to the sterilization of the medical devices; possible...

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

Class II — Potential Health HazardOngoing