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. 2,617 recalls have been distributed to Arkansas in the last 12 months.

49,990 total recalls
2,617 in last 12 months

Showing 1108111100 of 49,990 recalls

Medical DeviceAugust 26, 2022· Leica Microsystems, Inc.

Recalled Item: Leica Surgical Operating Microscopes Recalled by Leica Microsystems, Inc....

The Issue: During internal testing, Leica Microsystems has become aware of a component...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2022· Leica Microsystems, Inc.

Recalled Item: Leica Surgical Operating Microscopes Recalled by Leica Microsystems, Inc....

The Issue: During internal testing, Leica Microsystems has become aware of a component...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2022· Philips Respironics, Inc.

Recalled Item: Philips BiPAP A30 Recalled by Philips Respironics, Inc. Due to Motor...

The Issue: Motor assemblies manufactured with nonconforming plastic that contributes to...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 26, 2022· Philips Respironics, Inc.

Recalled Item: Philips BiPAP V30 Auto Recalled by Philips Respironics, Inc. Due to Motor...

The Issue: Motor assemblies manufactured with nonconforming plastic that contributes to...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 26, 2022· Philips Respironics, Inc.

Recalled Item: Philips OmniLab Advanced+ Intl (Flow Gen) Recalled by Philips Respironics,...

The Issue: Motor assemblies manufactured with nonconforming plastic that contributes to...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 26, 2022· Philips Respironics, Inc.

Recalled Item: Philips OmniLab Advanced + with Heated Tube Humidifier Recalled by Philips...

The Issue: Motor assemblies manufactured with nonconforming plastic that contributes to...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 26, 2022· Philips Respironics, Inc.

Recalled Item: Philips BiPAP A40 Recalled by Philips Respironics, Inc. Due to Motor...

The Issue: Motor assemblies manufactured with nonconforming plastic that contributes to...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 26, 2022· Philips Respironics, Inc.

Recalled Item: Philips OmniLab Advanced+ Recalled by Philips Respironics, Inc. Due to Motor...

The Issue: Motor assemblies manufactured with nonconforming plastic that contributes to...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 25, 2022· Zimmer, Inc.

Recalled Item: G7 Acetabular System Recalled by Zimmer, Inc. Due to The outer sterile...

The Issue: The outer sterile package cavity has a corner wall thickness that is below...

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

Class II — Potential Health HazardOngoing
FoodAugust 24, 2022· D. F. Stauffer Biscuit Co, Inc.

Recalled Item: White frosted animal cookies with multi-colored non-pareils in a 44oz...

The Issue: Potential contamination with foreign material (metal).

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 24, 2022· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista High Density Lipoprotein Cholesterol (HDLC) Flex reagent...

The Issue: Dimension Vista¿ High Density Lipoprotein Cholesterol (HDLC) Potential for...

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

Class II — Potential Health HazardOngoing
DrugAugust 23, 2022· Leading Pharma, LLC

Recalled Item: ClomiPRAMINE Hydrochloride Capsules Recalled by Leading Pharma, LLC Due to...

The Issue: Superpotent Drug: Assay value found to be 110.6% in Chlomipramine...

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

Class III — Low RiskOngoing
Refund
DrugAugust 23, 2022· Teva Pharmaceuticals USA Inc

Recalled Item: Neomycin Sulfate Tablets Recalled by Teva Pharmaceuticals USA Inc Due to...

The Issue: CGMP Deviations: A foreign matter identified as teflon was found in the...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 22, 2022· Pfizer Inc.

Recalled Item: PROPOFOL Injectable Emulsion Recalled by Pfizer Inc. Due to Presence of...

The Issue: Presence of particulate matter

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 22, 2022· CIPLA

Recalled Item: Difluprednate Ophthalmic Emulsion Recalled by CIPLA Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility: customer complaint for defective container...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 22, 2022· CIPLA

Recalled Item: Difluprednate Ophthalmic Emulsion Recalled by CIPLA Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility: customer complaint for defective container...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 22, 2022· SenTec AG

Recalled Item: sentec 24 / MARe-SF Multi-Site Attachment Ring Easy Recalled by SenTec AG...

The Issue: Weak skin adhesion.

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

Class II — Potential Health HazardOngoing
FoodAugust 19, 2022· Eden Foods, Inc

Recalled Item: Eden Organic Apple Juice in 32floz. Recalled by Eden Foods, Inc Due to...

The Issue: culling not performed to remove rotted apples, excessive levels of patulin...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 19, 2022· Lamb Weston Sales

Recalled Item: Item SP204 Recalled by Lamb Weston Sales Due to Potential Listeria Contamination

The Issue: Potential to be contaminated with Listeria monocytogenes.

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 19, 2022· Lamb Weston Sales

Recalled Item: Item GV020 Recalled by Lamb Weston Sales Due to Potential Listeria Contamination

The Issue: Potential to be contaminated with Listeria monocytogenes.

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

Class II — Potential Health HazardOngoing
Refund