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. 920 recalls have been distributed to Arkansas in the last 12 months.
Showing 46921–46940 of 49,990 recalls
Recalled Item: Seasonale(R) (Levonorgestrel/Ethinyl Estradiol Tablets) Recalled by Teva...
The Issue: Failed Impurity/Degradation Specification; an impurity identified as...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Camrese(TM) (Levonorgestrel/Ethinyl Estradiol Tablets) Recalled by Teva...
The Issue: Failed Impurity/Degradation Specifications; an impurity identified as...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: All Compounded Products Recalled by Med Prep Consulting, Inc. Due to Lack of...
The Issue: Lack of Assurance of Sterility; potential for mold contamination
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MUSCLEPHARM brand COMBAT POWDER (R) Recalled by F.H.G Corporation dba...
The Issue: One lot of each product may have extraneous materials due to a problem on...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: MUSCLEPHARM brand COMBAT POWDER (R) Recalled by F.H.G Corporation dba...
The Issue: One lot of each product may have extraneous materials due to a problem on...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Sunchang Ssamjang Sesame and Garlic Seasoned Bean Paste 500 g Recalled by...
The Issue: Sesame and Garlic Flavored Mixed Soy Bean Paste contains peanut powder which...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ADVIA Centaur Vitamin D Calibrator 2-pack Recalled by Siemens Healthcare...
The Issue: Negative bias in patient samples for Vitamin D
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur Vitamin D Calibrator 6-pack Recalled by Siemens Healthcare...
The Issue: Negative bias in patient samples for Vitamin D
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: epoc BGEM Test Card (Catalogue number CT-1004-00-00). quantitative testing...
The Issue: This recall is being initiated because the affected lots of this product may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rad-8 Pulse Oximeters The Rad-8 family of pulse oximeters and Recalled by...
The Issue: Masimo has identified a very small number (0.02%) of Rad-8 devices with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur Vitamin D Assay (500 tests) Recalled by Siemens Healthcare...
The Issue: Negative bias in patient samples for Vitamin D
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur Vitamin D Assay (100 tests) Recalled by Siemens Healthcare...
The Issue: Negative bias in patient samples for Vitamin D
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SLIDERPREP PLUS SLIDE PREPARATION CENTRIFUGE. Produce a monolayer of cells...
The Issue: Separation Technology, Inc. recalled SlidePrep Plus Cytology Centrifuges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Archer 0.035 inch (0.89mm) Super Stiff Guidewire Recalled by...
The Issue: Medtronic has identified an issue involving specific lot numbers of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Centricity Laboratory System is intended to be an information Recalled...
The Issue: GE Healthcare has become aware of a potential safety issue associated with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom Ultrasonics System 83 Plus 2 and Plus 9 Endoscope Washer/Disinfector....
The Issue: Certain System 83 Plus 2 and System 83 Plus 9 units running the Windows 7...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance CT 16-Slice Water Recalled by Philips Medical Systems (Cleveland)...
The Issue: Philips Healthcare received a report from the field stating when they viewed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hand Controls for Operon D750 Recalled by Berchtold Corp. Due to The firm...
The Issue: The firm received complaints for unintended movements.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Liothyronine Sodium Tablets Recalled by L. Perrigo Co. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: 3 month stability testing.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Portia (levonorgestrel and ethinyl estradiol) Tablets Recalled by Teva...
The Issue: Failed Tablet/Capsule Specifications: This recall is being carried out due...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.