Product Recalls in Wisconsin

Product recalls affecting Wisconsin — including food, drugs, consumer products, medical devices, and vehicles distributed to Wisconsin. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,850 recalls have been distributed to Wisconsin in the last 12 months.

52,482 total recalls
1,850 in last 12 months

Showing 4094140960 of 52,482 recalls

DrugFebruary 26, 2015· Pfizer Inc.

Recalled Item: Oxecta(TM) (oxycodone HCl) tablets Recalled by Pfizer 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
Medical DeviceFebruary 26, 2015· Ethicon Endo-Surgery Inc

Recalled Item: ENDOPATH ECHELON" Vascular White Reload for Advanced Placement Tip Recalled...

The Issue: During an internal inspection of the production process the firm discovered...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2015· Civco Medical Instruments Inc

Recalled Item: CIVCO Surgi-Tip Transducer Cover Sterile (15.2 x 244 cm) polyethylene...

The Issue: Leaks were detected in the recalled lot which may compromise the sterility...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2015· Biomet, Inc.

Recalled Item: Ziploop Button Product Usage: The Ziploop Button is a non-resorbable...

The Issue: The firm is recalling ToggleLocs and Ziploops manufactured in May and July...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2015· Orthovita, Inc., dBA Stryker Orthobiologics.

Recalled Item: Vitagel Recalled by Orthovita, Inc., dBA Stryker Orthobiologics. Due to...

The Issue: Several shipments of Vitagel product (a surgical hemostat) required to be...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2015· Biomet, Inc.

Recalled Item: ToggleLoc Recalled by Biomet, Inc. Due to The firm is recalling ToggleLocs...

The Issue: The firm is recalling ToggleLocs and Ziploops manufactured in May and July...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2015· Quest Medical, Inc.

Recalled Item: LIS27T - Lacrimal Intubation Set RX Only Sterile Used in Recalled by Quest...

The Issue: Expiration date incorrectly printed in Manufacturing Date field on both...

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

Class II — Potential Health HazardOngoing
DrugFebruary 25, 2015· Noven Pharmaceuticals, Inc.

Recalled Item: Minivelle (estradiol transdermal system) 0.05 mg/day Recalled by Noven...

The Issue: Temperature Abuse: Prolonged exposure to temperatures outside of labeled...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 25, 2015· Heritage Pharmaceuticals, Inc.

Recalled Item: Colistimethate for Injection USP Recalled by Heritage Pharmaceuticals, Inc....

The Issue: Lack of Assurance of Sterility: Firm is recalling two injectable products...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 25, 2015· Heritage Pharmaceuticals, Inc.

Recalled Item: RIFAMPIN for Injection Recalled by Heritage Pharmaceuticals, Inc. Due to...

The Issue: Lack of Assurance of Sterility: Firm is recalling two injectable products...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 25, 2015· Boston Scientific Corporation

Recalled Item: Various Lots of Expel Drainage Catheter with TwistLoc Hub Biliary Recalled...

The Issue: Complaints of device fragmentation after the catheter was implanted in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2015· Boston Scientific Corporation

Recalled Item: Boston Scientific: Expel" Drainage Catheter with Twist-Loc" Hub APDL...

The Issue: Boston Scientific is initiating this Medical Device Field Correction of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2015· Biosense Webster, Inc.

Recalled Item: LASSO NAV Duo Loop eco Catheters Recalled by Biosense Webster, Inc. Due to...

The Issue: Biosense Webster is recalling the LASSO NAV Duo Loop eco Catheters because...

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

Class II — Potential Health HazardOngoing
FoodFebruary 24, 2015· Maternal Science Inc

Recalled Item: Healthy Mama Boost it Up Pom Cherry Caffeine Free Protein Recalled by...

The Issue: Healthy Mama Brand dietary supplements contain undeclared milk.

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 24, 2015· Maternal Science Inc

Recalled Item: Healthy Mama Boost it Up Mango with Ginger Caffeine Free Recalled by...

The Issue: Healthy Mama Brand dietary supplements contain undeclared milk.

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 24, 2015· Maternal Science Inc

Recalled Item: Healthy Mama Boost It Up Mighty Mango Caffeine Free Protein Recalled by...

The Issue: Healthy Mama Brand dietary supplements contain undeclared milk.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceFebruary 24, 2015· Synthes, Inc.

Recalled Item: Synthes 130 Degree Aiming Arm and 125 Degree Aiming Arm Recalled by Synthes,...

The Issue: The guide sleeve has the potential to jam in the Aiming Arms, which may...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2015· LeMaitre Vascular, Inc.

Recalled Item: LeMaitre Vascular Tumescent Catheter Inversion (TCI) System. The TCI System...

The Issue: Mislabeled with an incorrect expiration date

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

Class III — Low RiskOngoing
DrugFebruary 23, 2015· Qualitest Pharmaceuticals

Recalled Item: PROMETHAZINE DM SYRUP (Promethazine Hydrochloride Recalled by Qualitest...

The Issue: Presence of Foriegn Substance: Plastic cap closure particulates may be...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 23, 2015· Sagent Pharmaceuticals Inc

Recalled Item: Atracurium Besylate Injection Recalled by Sagent Pharmaceuticals Inc Due to...

The Issue: Lack of Assurance of Sterility: Recall initiated due to FDA observations...

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

Class II — Potential Health HazardOngoing
Refund