Archive
534 recalls were announced in January 2020.
Of the 534 recalls this month scored against our rubric, 7% are Critical, 43% are Severe.
Which agencies issued them
Dierbergs Markets is recalling 211 units of Grilled Chicken Cobb Salad because hardboiled eggs used in the product were potentially contaminated with Listeria monocytogenes.
Dierbergs Markets is recalling Creamy Red Potato Salad because it was made with hardboiled eggs potentially contaminated with Listeria monocytogenes.
Middlefield Original Cheese Coop is recalling shredded mozzarella cheese due to potential Listeria monocytogenes contamination. The product was distributed to a single consignee in Ohio.
Motto International Corp is recalling Rhino 7 Platinum 30000 Capsules because FDA analysis found the product contains tadalafil, an unapproved active ingredient.
Fresh Unlimited Inc is recalling Garden Salad Kits because eggs used in their manufacture may be contaminated with Listeria monocytogenes.
Dierbergs Markets is recalling Kosher-Style Potato Salad because it was made with hardboiled eggs potentially contaminated with Listeria monocytogenes.
Cheesewich Factory is recalling RTE bacon and eggs packages due to potential Listeria monocytogenes contamination.
Middlefield Original Cheese Coop is recalling shredded cheddar cheese due to potential Listeria monocytogenes contamination. The product was distributed to a single consignee in Ohio.
Dierbergs Markets is recalling Deviled Egg Salad because the hardboiled eggs used were potentially contaminated with Listeria monocytogenes.
Dierbergs Markets is recalling 456 salad kits because they contain hardboiled eggs potentially contaminated with Listeria monocytogenes.
Motto International Corp is recalling Panther Platinum 30000 Capsules because FDA analysis found the product contains tadalfil and was marketed without an approved NDA or ANDA.
Motto International Corp is recalling Bull Platinum 30000 Capsules because FDA analysis found the product contains tadalafil, a prescription drug, and it was marketed without an approved NDA or ANDA.
Middlefield Original Cheese Coop is recalling shredded mozzarella and provolone mix cheese due to potential Listeria monocytogenes contamination. The product was distributed to a single consignee in Ohio.
Gourmet International Ltd. is recalling Butler's Dark Chocolate with Irish Whisky bars due to undeclared milk. The recall affects 2,000 units distributed across 15 states.
Motto International Corp is recalling Stallion Platinum 30000 Capsules because FDA analysis found the unapproved product contains tadalafil.
Assurance Infusion is recalling BUP 21MG/CLON 252MCG/MORP 20MG/ML Injection syringes due to a lack of sterility assurance. The recall covers products distributed nationwide.
Assurance Infusion is recalling specific lots of Hydromorphone 3mg/mL injection syringes due to a lack of sterility assurance. The products were distributed nationwide.
Assurance Infusion is recalling specific lots of Morphine 30mg/mL injection syringes due to a lack of sterility assurance. The affected products were distributed nationwide.
Assurance Infusion is recalling specific lots of a multi-drug injection syringe due to a lack of sterility assurance.
Assurance Infusion is recalling specific lots of Baclofen injection syringes due to a lack of sterility assurance. The product was distributed nationwide.
Assurance Infusion is recalling two syringes of Phenol 2.5% Sterile Solution because of a lack of sterility assurance.
Assurance Infusion is recalling specific syringes containing a combination of drugs due to a lack of sterility assurance.
Assurance Infusion is recalling 166 vials of Testosterone Cypionate 200mg/mL oil injection due to a lack of sterility assurance. The product was distributed nationwide.
Assurance Infusion is recalling 20 mL syringes of BUP 15MG/CLON 300MCG/FENT 1500MCG/ML injection due to a lack of sterility assurance.
Assurance Infusion is recalling BUP 3 mg/MORP 15 mg/mL Injection syringes due to a lack of sterility assurance. The recall covers specific lots distributed nationwide.
Assurance Infusion is recalling specific lots of Buprenorphine and Fentanyl injection due to a lack of sterility assurance.
Edwards Lifesciences is recalling QuickDraw Venous Cannulas because the device may separate from its connector if used for more than six hours, potentially causing significant blood loss.
Assurance Infusion is recalling specific lots of Morphine 7mg/mL injection syringes due to a lack of sterility assurance. The product was distributed nationwide.
Assurance Infusion is recalling specific lots of Buprenorphine and Morphine injection due to a lack of sterility assurance. The product was distributed nationwide.
Assurance Infusion is recalling Bi-Mix Forte 30 mg/2 mg/mL injections because of a lack of sterility assurance. The affected lot was distributed nationwide.
Assurance Infusion is recalling specific lots of Hydromorphone 5mg/mL injections because they may lack sterility assurance.
Assurance Infusion is recalling BUP 20MG/SUF 105MCG/ML Injection in 20 mL syringes due to a lack of sterility assurance. The recall is nationwide.
Assurance Infusion is recalling 20 mL syringes of BUP 30MG/FENT 750MCG/HYDROM 15MG/ML injection due to a lack of sterility assurance.
Assurance Infusion is recalling QUADMIX in 1 mL vials because of a lack of sterility assurance. The affected lot was distributed nationwide.
Assurance Infusion is recalling Bi-Mix 30 mg/1 mg/mL injections because of a lack of sterility assurance. The affected vials were distributed nationwide.
Assurance Infusion is recalling Hydromorphone 4mg/mL injection syringes due to a lack of sterility assurance. The product was distributed nationwide.
Assurance Infusion is recalling specific syringes of Baclofen, Fentanyl, and Morphine injection due to a lack of sterility assurance.
Assurance Infusion is recalling specific lots of BUP 40MG/FENT 1200MCG/SUF 400MCG/ML INJ in 20 mL syringes due to a lack of sterility assurance.
Assurance Infusion is recalling specific lots of Testosterone Cypionate 200mg/mL injections due to a lack of sterility assurance. The affected products were distributed nationwide.
Assurance Infusion is recalling specific lots of Sufentanil 300mcg/mL injection syringes due to a lack of sterility assurance.
Trilliant Surgical is recalling 20 Gridlock Ankle Screw Driver Bits because they are out of specification and may fail to retain screws during implant procedures.
Assurance Infusion is recalling specific lots of Clonazepam and Fentanyl injection due to a lack of sterility assurance. The product was distributed nationwide.
Assurance Infusion is recalling specific lots of Sufentanil 55.5 mcg/mL injection syringes due to a lack of sterility assurance.
GE Healthcare is recalling 12 units of the Airway Gas Option N-CAiO because displayed oxygen values may be incorrect, potentially causing up to 50% measurement error.
Assurance Infusion is recalling specific lots of Testosterone Cypionate 200mg/mL oil due to a lack of sterility assurance. The affected vials were distributed nationwide.
Assurance Infusion is recalling a specific lot of Clonidine and Morphine injection due to a lack of sterility assurance. The product was distributed nationwide.
GE Healthcare is recalling 161 CARESCAPE Respiratory Module E-sCAiO units because displayed oxygen values may be incorrect, potentially causing up to 50% measurement error.
Assurance Infusion is recalling specific lots of Morphine 10mg/mL injection syringes nationwide due to a lack of sterility assurance.
Assurance Infusion is recalling 20 vials of Trimix Forte Plus injection due to a lack of sterility assurance. The product was distributed nationwide.
Assurance Infusion is recalling BUP 5.3MG/FENT 1050 MCG/ML Injection in 20 mL syringes due to a lack of sterility assurance.
Assurance Infusion is recalling BUP 3MG/HYDROM 15MG/ML INJ syringes due to a lack of sterility assurance. The recall covers nationwide distribution.
Assurance Infusion is recalling specific lots of Autologous Serum 20% Eye Drops because of a lack of sterility assurance.
Assurance Infusion is recalling specific lots of Buprenorphine and Morphine injection due to a lack of sterility assurance. The affected product was distributed nationwide.
Assurance Infusion is recalling BUP 2MG/HYDROM 2MG/ML Injection syringes due to a lack of sterility assurance. The recall covers nationwide distribution.
GE Healthcare is recalling 37 CARESCAPE Respiratory Modules because displayed oxygen values may be incorrect, potentially causing up to 50% measurement error.
Assurance Infusion is recalling Hydromorphone 15mg/mL injection syringes due to a lack of sterility assurance. The product was distributed nationwide.
Toyota is recalling 1997-2000 Celica, RAV4, and Supra vehicles because driver air bag inflators may rupture or underinflate in a crash.
Assurance Infusion is recalling specific lots of Sufentanil 150mcg/mL injection syringes due to a lack of sterility assurance.
GE Healthcare is recalling three CARESCAPE Respiratory Module E-sCOVX units because displayed oxygen values may be incorrect, potentially causing up to 50% measurement error.
Hikma Pharmaceuticals is recalling specific lots of Ketorolac Tromethamine Injection because of the presence of polydimethylsiloxane particles.
Assurance Infusion is recalling specific lots of Trimix Forte 4 injection because the product may lack sterility assurance.
Assurance Infusion is recalling BUP 35MG/FENT 1.5MG/ML in 20 mL syringes due to a lack of sterility assurance. The affected lot was distributed nationwide.
Assurance Infusion is recalling specific lots of Morphine 2mg/mL injection syringes due to a lack of sterility assurance.
Assurance Infusion is recalling a specific lot of buprenorphine and fentanyl injection due to a lack of sterility assurance. The product was distributed nationwide.
Assurance Infusion is recalling specific syringes of a multi-drug injection due to a lack of sterility assurance. The product was distributed nationwide.
Assurance Infusion is recalling QUADMIX FORTE in 1 mL vials because of a lack of sterility assurance. The recall covers 5 vials distributed nationwide.
Assurance Infusion is recalling specific lots of Morphine 5mg/mL injection syringes due to a lack of sterility assurance.
Assurance Infusion is recalling 45 vials of Trimix Super injection nationwide due to a lack of sterility assurance.
Assurance Infusion is recalling a specific lot of BUP 20MG/CLON 300MCG/FENT 2000MCG/ML Injection due to a lack of sterility assurance.
Assurance Infusion is recalling specific lots of Hydromorphone 6mg/mL injection due to a lack of sterility assurance.
Assurance Infusion is recalling specific syringes of a multi-drug injection due to a lack of sterility assurance. The product was distributed nationwide.
Assurance Infusion is recalling BUP 20MG/SUF 1000MCG/ML Injection syringes due to a lack of sterility assurance. The recall covers nationwide distribution in the United States.
Assurance Infusion is recalling specific lots of Buprenorphine and Fentanyl injection due to a lack of sterility assurance.
Assurance Infusion is recalling Morphine 15mg/mL injection syringes due to a lack of sterility assurance. The recall covers products distributed nationwide in the United States.
Assurance Infusion is recalling specific lots of a Clonazepam and Morphine injection because of a lack of sterility assurance. The product was distributed nationwide.
Assurance Infusion is recalling specific lots of Buprenorphine and Hydromorphone injection due to a lack of sterility assurance.
Sun Pharmaceutical Industries is recalling 207,585 blisters of Sumatriptan Succinate 100 mg tablets due to failed impurity specifications.
Assurance Infusion is recalling 19 vials of CJC-1295 and Ipamorelin injections nationwide due to a lack of sterility assurance.
Assurance Infusion is recalling specific lots of BUP 10MG/HYDROM 15MG/SUF 200MCG/ML Injection syringes due to a lack of sterility assurance.
GE Healthcare is recalling 59 CARESCAPE Respiratory Modules because displayed oxygen values may be incorrect, potentially causing up to 50% measurement error.
Assurance Infusion is recalling a specific lot of multi-drug injection syringes due to a lack of sterility assurance. The product was distributed nationwide.
Sun Pharmaceutical Industries is recalling Testosterone Cypionate for Injection due to cGMP deviations and similarity to a previously rejected out-of-specification lot.
Assurance Infusion is recalling specific lots of Baclofen and Hydromorphone injection due to a lack of sterility assurance.
Assurance Infusion is recalling specific lots of Hydromorphone 2mg/mL injection syringes because of a lack of sterility assurance.
Assurance Infusion is recalling specific lots of Baclofen and Hydromorphone injection due to a lack of sterility assurance. The affected product was distributed nationwide.
Assurance Infusion is recalling BPC-157 vials nationwide because the product lacks sterility assurance.
Assurance Infusion is recalling Buprenorphine and Hydromorphone Injection in 20 mL syringes due to a lack of sterility assurance. The product was distributed nationwide.
Physio-Control is recalling 705 LIFEPAK 15 Monitor/Defibrillator service kits because oxidation may prevent the device from delivering a shock.
Assurance Infusion is recalling BUP 8MG/CLON 100MCG/HYDROM 20MG/ML Injection syringes due to a lack of sterility assurance.
Assurance Infusion is recalling BUP 4MG/FENT 3000MCG/ML Injection in 20 mL syringes due to a lack of sterility assurance.
Assurance Infusion is recalling Hydrom 1mg/Morp 20mg/Suf 100mcg/mL injection syringes due to a lack of sterility assurance.
Assurance Infusion is recalling BUP 675MCG/MORP 20MG/ML Injection syringes due to a lack of sterility assurance.
Assurance Infusion is recalling specific lots of Baclofen and Fentanyl Injection due to a lack of sterility assurance. The product was distributed nationwide.
Assurance Infusion is recalling specific lots of HCG 10,000U/1ML injections due to a lack of sterility assurance. The affected products were distributed nationwide.
Veggie Noodle Co is recalling Cece's Veggie Co. brand Fresh Veggie Ramen with Chicken Broth due to potential contamination with Listeria monocytogenes.
Assurance Infusion is recalling a specific lot of BAC/FENT/MORP injection due to a lack of sterility assurance. The product was distributed nationwide.
Assurance Infusion is recalling BUP 23MG/HYDROM 25MG/SUF 100MCG/ML Injection syringes due to a lack of sterility assurance. The recall covers nationwide distribution.
Assurance Infusion is recalling Morphine Sulfate Injection in 20 mL syringes due to a lack of sterility assurance. The product was distributed nationwide.
Assurance Infusion is recalling HCG 1,000U/1ML injection vials nationwide due to a lack of sterility assurance. Consumers should stop using the product and contact their healthcare provider.
Assurance Infusion is recalling specific lots of Baclofen and Hydromorphone injection due to a lack of sterility assurance.
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