Product Recalls in Wyoming
Product recalls affecting Wyoming — including food, drugs, consumer products, medical devices, and vehicles distributed to Wyoming. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,364 recalls have been distributed to Wyoming in the last 12 months.
Showing 31101–31120 of 48,219 recalls
Recalled Item: RayStation 2.5 Recalled by RAYSEARCH LABORATORIES AB Due to RaySearch became...
The Issue: RaySearch became aware of the problem as it was discovered in cooperation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sealapex Xpress Recalled by Ormco/Sybronendo Due to SybronEndo is recalling...
The Issue: SybronEndo is recalling the Sealapex Xpress because it was labeled with an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ramipril Capsules Recalled by Actavis Laboratories, FL, Inc. Due to...
The Issue: Labeling: Incorrect or Missing Lot And/or Exp Date: Bottles labeled with the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Entenmann's Little Bites Variety - 20 pouches labeled for resale Recalled by...
The Issue: Presence of plastic in muffins and brownies.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Entenmann's Little Bites Fudge Brownies - 20 muffins Recalled by BIMBO...
The Issue: Presence of plastic in muffins and brownies.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Entenmann's Little Bites Chocolate Chip Muffins Recalled by BIMBO Bakeries...
The Issue: Presence of plastic in muffins and brownies.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Carry bar which is an accessory to a lift used Recalled by ErgoSafe...
The Issue: The black plastic puck on the carry bar is breaking resulting in potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE/ IMMULITE 1000 Systems CMM CMV IgM Assay Recalled by Siemens...
The Issue: Multiple customers reported seeing an increase in imprecision with some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE 2000/IMMULITE 2000XPi Systems CMM CMV IgM Assay Recalled by Siemens...
The Issue: Multiple customers reported seeing an increase in imprecision with some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZENATANE (isotretinoin capsules USP) 20 mg Recalled by Dr. Reddy's...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BioFlo PICC with ENDEXO and PASV Valve Technology Maximal Barrier Recalled...
The Issue: Medline Industries, Inc. supplies Navilyst with sterile package gloves...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioFlo PICC with ENDEXO Technology Maximal Barrier Nursing Kit - Recalled by...
The Issue: Medline Industries, Inc. supplies Navilyst with sterile package gloves...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Xcela Power Injectable PICC Maximal Barrier Nursing Kit The Maximal Recalled...
The Issue: Medline Industries, Inc. supplies Navilyst with sterile package gloves...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TANDEM (TM) COCR SHELL UHMWPE LINER BIPOLAR Recalled by Smith & Nephew, Inc....
The Issue: Some Bipolar shells were manufactured with an out of specification retainer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LFIT Anatomic V40 Femoral Head Recalled by Stryker Howmedica Osteonics Corp....
The Issue: Stryker received several complaints describing incidence of harm secondary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TANDEM (TM) INTL COCR SHELL UHMWPE LINER BIPOLAR Recalled by Smith & Nephew,...
The Issue: Some Bipolar shells were manufactured with an out of specification retainer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CONCEPT HEATWAVE Electrode 130 mm x 2.3 mm diameter Recalled by ConMed...
The Issue: CONMED received complaints of damage to the CS-023 electrodes shaft...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TriMed Semi-Tubular Plate Recalled by Trimed Inc Due to TriMed is recalling...
The Issue: TriMed is recalling the Semi-Tubular Plates with 10 holes (SMTP-10) because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dietary Supplement Acidophilus Blend Recalled by Complete Packaging &...
The Issue: Nature's Power Solutions Acidophilus Blend due to undeclared milk allergen.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Willy Rusch GmbH Tracheostomy Tube Set Cannulation of tracheotomised...
The Issue: The connector may disconnect from the tracheostomy tube during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.