Product Recalls in South Dakota
Product recalls affecting South Dakota — including food, drugs, consumer products, medical devices, and vehicles distributed to South Dakota. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,452 recalls have been distributed to South Dakota in the last 12 months.
Showing 17001–17020 of 27,558 recalls
Recalled Item: Safety-Deluxe Lumbar Puncture Tray Recalled by Robert Busse & Co. Inc....
The Issue: BD SafetyGlide Needle 22GA 1-1/2 inch may contain the presence of loose...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Safety-Deluxe Lumbar Puncture Tray Recalled by Robert Busse & Co. Inc....
The Issue: BD SafetyGlide Needle 22GA 1-1/2 inch may contain the presence of loose...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Safety Deluxe Bone Marrow Biopsy/ Aspiration Tray with Biopsy Needle...
The Issue: BD SafetyGlide Needle 22GA 1-1/2 inch may contain the presence of loose...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Safety-Deluxe Basic Soft Tissue Biopsy Tray without Biopsy Needle Recalled...
The Issue: BD SafetyGlide Needle 22GA 1-1/2 inch may contain the presence of loose...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NOVADAQ SPY-PHI Drape Recalled by NOVADAQ TECHNOLOGIES INC. Due to The...
The Issue: The sterile drape material may contain a pinhole compromising its integrity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NOVADAQ SPY-PHI PAQ Intended for use with the SPY-PHI System Recalled by...
The Issue: The sterile drape material may contain a pinhole compromising its integrity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Converters(R) Tiburon(R) Arthroscopy Drape Recalled by Cardinal Health 200,...
The Issue: Outer label of some units of product number/lot number 8482, Lot 16LFS235...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NOVADAQ SPY-PHI Drape Recalled by NOVADAQ TECHNOLOGIES INC. Due to The...
The Issue: The sterile drape material may contain a pinhole compromising its integrity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lumbar Puncture Tray Recalled by Robert Busse & Co. Inc. d.b.a. Busse...
The Issue: BD SafetyGlide Needle 22GA 1-1/2 inch may contain the presence of loose...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tomcat Instrument Recalled by Hologic, Inc Due to A Tomcat Instrument...
The Issue: A Tomcat Instrument software anomaly that causes the pipettor arm to make...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Safety Deluxe Bone Marrow Biopsy/Aspiration Tray Recalled by Robert Busse &...
The Issue: BD SafetyGlide Needle 22GA 1-1/2 inch may contain the presence of loose...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Converters(R) Under Buttocks Drape with Fluid Control Pouch II Recalled by...
The Issue: Outer label of some units of product number/lot number 8482, Lot 16LFS235...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Laceration Tray Recalled by Robert Busse & Co. Inc. d.b.a. Busse Hospital...
The Issue: BD SafetyGlide Needle 22GA 1-1/2 inch may contain the presence of loose...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alere iScreen Dx Urine Drug Screen Card Recalled by Ameditech Inc Due to The...
The Issue: The kit box label incorrectly identifies PCP (instead of TCA) as one of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Coulter LH 750 Recalled by Beckman Coulter Inc. Due to Beckman Coulter has...
The Issue: Beckman Coulter has determined that additional clarification for the Blast...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cobalt HV Bone Cement 40GM Recalled by Encore Medical, Lp Due to Loss of the...
The Issue: Loss of the seal on the sterile Tyvek packaging used with this Cobalt Bone...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Burn Sheet Recalled by Certified Safety Mfg Inc Due to Burn Sheet has...
The Issue: Burn Sheet has possibility of being shredded.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stroke Fast Pack(TM) Trevo XP ProVue Retriever 4 x 20 Recalled by Stryker...
The Issue: Stryker Neurovascular has become aware that some 3-Pack Stroke Fast Packs...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stroke Fast Pack(TM) Trevo XP ProVue Retriever 3 x 20 Recalled by Stryker...
The Issue: Stryker Neurovascular has become aware that some 3-Pack Stroke Fast Packs...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cobalt MV with Gentamicin Recalled by Encore Medical, Lp Due to Loss of the...
The Issue: Loss of the seal on the sterile Tyvek packaging used with this Cobalt Bone...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.