Archive
585 recalls were announced in August 2015.
Of the 585 recalls this month scored against our rubric, 13% are Critical, 15% are Severe.
Which agencies issued them
Chrysler is recalling 2015 Jeep Renegade vehicles to fix a radio software vulnerability that could allow unauthorized remote control of vehicle systems.
Charles Products Inc. is recalling specific shot glasses because testing revealed lead and cadmium levels exceeding FDA guidance.
Paleteria La Jalpita is recalling 90 units of La Jalpita brand walnut bolis in Oregon and Washington due to undeclared milk.
Medtronic is recalling 1,415 Passive Biopsy Needle Kits because compromised adhesive may cause the sphere assembly to move, leading to inaccurate navigation during brain biopsies.
Medtronic is recalling 1,415 Passive Biopsy Needle Kits because adhesive failure may cause the sphere assembly to move, leading to inaccurate navigation during brain biopsies.
The Apothecary Shoppe LLC is recalling SIU-Phent .4 mg/PGE1 20 mcg/mL Injection due to a lack of documentation for environmental monitoring during production.
The Apothecary Shoppe is recalling specific lots of SIU-Papav/Phentol 30/1 mg/mL Injection due to a lack of documentation for environmental monitoring during production.
Cook Inc. is recalling Beacon Tip Royal Flush Plus High-Flow Catheters due to reports of tip splits or separation that may cause loss of function or complications.
The Apothecary Shoppe LLC is recalling SIU-Tri-Mix 30/2/20 Injection in Oklahoma due to a lack of documentation proving proper environmental monitoring during production.
The Apothecary Shoppe LLC is recalling specific vials of Papaverine and Phentolamine Injection due to a lack of documentation confirming proper environmental monitoring during production.
Charles Products Inc. is recalling pint-sized glasses with decorative artwork because testing revealed lead and cadmium levels exceeding FDA guidance.
Supervalu, Inc. is recalling Caramel Danish Rolls because they may contain undeclared milk, a major food allergen.
Nissan is recalling 2012-2015 Versa and 2014-2015 Versa Note vehicles because a center console trim panel may catch the driver's shoe, delaying brake application and increasing crash risk.
Pierce is recalling 2014-2015 Velocity and Quantum vehicles because LED headlamps may flicker in extreme cold, reducing visibility and increasing crash risk.
Winnebago is recalling 2014-2015 Itasca and Winnebago motorhomes because deadbolt locks may become stuck, potentially trapping occupants inside the vehicle.
Siemens Medical Solutions is recalling Biograph 64-3R TruePoint systems because they may be missing a locking ring on optional ceiling mounts.
Teva Pharmaceuticals is recalling specific lots of amphetamine tablets because they failed impurity specifications. The product contains an unknown impurity.
Siemens Medical Solutions is recalling specific CT systems because optional ceiling mounts may be missing a locking ring.
The Anspach Effort, Inc. is recalling Synthes Battery Power Line II Oscillator Model 530.710 units because the saw head may separate from the drive unit or come loose.
The Apothecary Shoppe is recalling specific lots of Testosterone Cypionate Injection due to a lack of documentation confirming proper environmental monitoring during production.
Siemens Medical Solutions USA Inc. is recalling one Biograph mCT S(64)-4R unit because it may be missing a locking ring on the optional ceiling mount.
Siemens is recalling ACUSON S Family ultrasound systems because biopsy needles may move outside the on-screen guidelines when using specific attachments.
Cowden's Lycoming Bakery is recalling 123 units of 2-pack pizza shells because they contain whey, a milk allergen, that was not listed on the label.
Paleteria La Jalpita is recalling Coco (Coconut) Popsicles due to undeclared sulfite. The product was distributed in Oregon and Washington.
Philips is recalling 13,168 HeartStart XL+ defibrillators worldwide due to software and hardware issues that can affect device function.
The Apothecary Shoppe is recalling S-Methylcobalamin 1000 mcg/mL Injection because documentation for environmental monitoring during production was missing.
Siemens Medical Solutions is recalling Axiom Artis angiography systems because liquid may seep through the top cover and penetrate internal components, potentially disabling table movements.
Siemens is recalling one Biograph mCT S(40)-4R unit because it may be missing a locking ring on the optional ceiling mount.
Mondelez International is recalling Nabisco Fig Newtons because the outer carton fails to declare milk, a major allergen, while the inner packaging does.
Inn Foods Inc. is recalling IQF Italian Cut Green Beans after a sample tested positive for Listeria monocytogenes.
Maya Overseas Foods is recalling approximately 8,000 lbs of Maya brand Cashew Split due to potential Salmonella contamination. The product was distributed in New York, New Jersey, Pennsylvania, Connecticut, Massachusetts, and Florida.
Osamu Corporation is recalling raw frozen saku tuna products from Indonesia due to potential Salmonella contamination. The recall covers bulk frozen tuna distributed to 15 U.S. states and D.C.
Paleteria La Jalpita is recalling Gelleta (Cookies) popsicles due to undeclared soy lecithin and wheat. The product was distributed in Oregon and Washington.
Pinnacle Foods is recalling Wish-Bone Ranch Dressing because it contains undeclared eggs, posing a risk to consumers with egg allergies.
The Apothecary Shoppe LLC is recalling SO-Acetylcysteine 10% Sterile Ophthalmic Solution due to lack of documentation for environmental monitoring during production.
Siemens Medical Solutions is recalling Artis zee angiography systems because liquid may seep through the table cover, potentially preventing table movement.
Titan Spine is recalling specific Endoskeleton TCS Integrated Locking Bone Screw Assemblies because the locking collars are not locking.
The Apothecary Shoppe LLC is recalling SIU-Prostaglandin E1 500 mcg/mL Injection vials in Oklahoma due to lack of documentation for environmental monitoring during production.
Osamu Corporation is recalling raw frozen ground tuna from Indonesia due to potential Salmonella contamination. The products were distributed to 15 states and DC.
Midlon Foods Inc. is recalling 5,472 units of Maria Biscuits because misaligned labels covered the allergen warning statement.
The Apothecary Shoppe LLC is recalling SIU-Prostaglandin E1 20 mcg/mL Injection due to a lack of documentation ensuring proper environmental monitoring during production.
Merge Healthcare is recalling 451 Merge Hemo systems used with Masimo PHASEIN modules due to system freeze-ups that required moving patients to other cath labs.
Flowers By Zoe is recalling girls' striped hoodies and tie-dye jackets because neck drawstrings pose a strangulation hazard to children.
Cook Inc. is recalling Beacon Tip Torcon NB Advantage Catheters due to reports of tip splits or separation, which may cause loss of function or complications.
Osamu Corporation is recalling raw frozen tuna loin products from Indonesia due to potential Salmonella contamination. The recall affects bulk frozen tuna distributed to 15 U.S. states and D.C.
Chrysler is recalling 2014 Jeep Cherokee vehicles because using front wipers on dry glass may damage the body control module, potentially causing wiper failure and impaired vision.
Siemens Medical Solutions is recalling specific Biograph 6-4R CT systems because they may be missing a locking ring on optional ceiling mounts.
The Apothecary Shoppe is recalling HCG 1000 U/mL Injection vials because proper environmental monitoring documentation was missing during production.
The Apothecary Shoppe is recalling SIU-Tri-Mix vials because documentation for environmental monitoring during production was missing, raising concerns about sterility.
The Apothecary Shoppe LLC is recalling specific vials of Papaverine and Phentermine Injection due to a lack of documentation proving proper environmental monitoring during production.
Ranbaxy Inc. is recalling 9,229 boxes of Absorica LD (isotretinoin) capsules because the capsule shells contain undeclared FD&C Yellow No. 5.
Roche is recalling S2 Fluid Packs for the Cobas b 221 system because they may generate a transponder error, preventing the instrument from starting measurements.
The Apothecary Shoppe LLC is recalling SIU-Phentolamine 5 mg/mL vials in Oklahoma due to lack of documentation for environmental monitoring during production.
The Apothecary Shoppe LLC is recalling SIU-Papaverine 30 mg/mL Injection due to a lack of documentation ensuring proper environmental monitoring during production.
Zimmer Surgical Inc. is recalling 330 units of 30-inch tourniquet cuffs because the instructions for use were missing usage instructions and warnings.
The Apothecary Shoppe is recalling S-methylcobalamin 25 mg/mL injection vials because documentation for environmental monitoring during production was missing.
Siemens Medical Solutions is recalling two Biograph mCT X-4R systems because they may be missing a locking ring on optional ceiling mounts.
The Apothecary Shoppe is recalling Hydroxyprogesterone Caproate 250 vials due to lack of documentation for environmental monitoring during production.
The Apothecary Shoppe is recalling SIU-Tri-Mix 24/1/20 Injection vials because documentation for environmental monitoring during production was missing, raising concerns about sterility.
Siemens Medical Solutions USA Inc. is recalling two Biograph 64-4R CT systems because they may be missing a locking ring on optional ceiling mounts.
The Apothecary Shoppe is recalling SIU-Tri-Mix Injection Solution because proper environmental monitoring documentation was missing during production.
Paleteria La Jalpita is recalling 420 units of Limon (Lemon) Bolis in Oregon and Washington due to undeclared Yellow No. 5.
GE Healthcare is recalling 82 MRI scanners because a missing spacer may cause images to be flipped left-right with incorrect orientation annotations.
MedOp Health, Inc. is recalling MaxiFlex Multinutrient Formula dietary supplements because a material review found the Chondroitin Sulfate raw material used was out of specification.
Paleteria La Jalpita is recalling 945 units of La Jalpita brand mango popsicles distributed in Oregon and Washington due to undeclared Yellow No. 6.
Paleteria La Jalpita is recalling Vanilla popsicles due to undeclared Yellow No. 5 and Yellow No. 6.
Paleteria La Jalpita is recalling pineapple popsicles in Oregon and Washington due to undeclared Yellow No. 5 and Yellow No. 6.
The Apothecary Shoppe is recalling specific vials of Papaverine and Phentolamine Injection because documentation for environmental monitoring during production was missing.
The Apothecary Shoppe LLC is recalling SIU-Tri-Mix 30/1/20 Injectable in Oklahoma due to a lack of documentation ensuring proper environmental monitoring during production.
Paleteria La Jalpita is recalling 1,890 units of Rompope bolis in Oregon and Washington due to undeclared Yellow No. 5.
Paleteria La Jalpita is recalling Pepino c/ Chile popsicles due to undeclared Yellow No. 5. The product was distributed in Oregon and Washington.
The Apothecary Shoppe LLC is recalling S-Methylcobalamin 5000 mcg/mL Injection in 750 mL containers due to a lack of assurance of sterility.
The Apothecary Shoppe LLC is recalling SIU-Tri-Mix 18/1/10 Injection because proper environmental monitoring documentation was missing during production.
The Apothecary Shoppe LLC is recalling SIU-Tri-Mix 20/1 mg/10 mcg/mL vials because proper environmental monitoring documentation was missing during production.
The Apothecary Shoppe is recalling SIU-Phent .8/PGE1 20 mcg/mL Injection vials because proper environmental monitoring documentation was missing during production.
The Apothecary Shoppe LLC is recalling SIH-Testosterone Cypionate Injection because proper environmental monitoring documentation is missing, raising concerns about sterility.
The Apothecary Shoppe LLC is recalling SIU-Tri-Mix 17/0.6/5.7 Injectable in Oklahoma due to lack of assurance of sterility from missing environmental monitoring documentation.
Atrium Medical Corporation is recalling 620 units of 36Fr Right Angled Firm PVC Thoracic Catheters due to incorrect labeling on inner pouches.
The Apothecary Shoppe LLC is recalling SIU-Tri-Mix 30/1/10 Injection vials in Oklahoma due to a lack of documentation for environmental monitoring during production.
Paleteria La Jalpita is recalling 1,350 units of Vanilla bolis (tube) sold in Oregon and Washington due to undeclared Yellow No. 6.
Siemens Medical Solutions is recalling Artis Q angiography systems because liquid may seep through the top cover, potentially disabling table movements. No injuries have been reported.
Paleteria La Jalpita is recalling Pistachio-Pistache popsicles due to undeclared Yellow No. 5. The product was distributed in Oregon and Washington.
Siemens Medical Solutions is recalling three Biograph mCT Flow Edge-4R systems because they may be missing a locking ring on optional ceiling mounts.
Olympus Scientific Solutions Americas is recalling 1,047 Analytical X-ray Systems because scatter readings around the probe head were higher than published specifications for certain samples.
Paleteria La Jalpita is recalling Nance popsicles because they contain undeclared Yellow No. 6, a food dye.
Church & Dwight is recalling Lil Critters Gummy Vites Complete Multivitamin because two lots were produced using Adult Multivitamin bulk.
The Apothecary Shoppe is recalling SIU-Tri-Mix 18/1/20 Injection because documentation for environmental monitoring during production was missing.
Zimmer Surgical Inc. is recalling 61 units of 18-inch disposable tourniquet cuffs because the folded instructions for use pamphlet was missing usage instructions and warnings.
Medtronic is recalling EnVeo R Loading Systems because of the presence of particulate. The recall affects 6,912 units worldwide, including 540 in the US.
Perrigo Israel Pharmaceuticals is voluntarily recalling 158,268 tubes of Mometasone Furoate Ointment USP, 0.1%, because the product is subpotent.
Shionogi Inc. is recalling Nisoldipine Extended Release Tablets, 17 mg, because they failed to meet dissolution specifications. The recall covers products distributed nationwide and in Puerto Rico.
GlaxoSmithKline is recalling Panadol Extra Strength acetaminophen bottles in Puerto Rico and the Virgin Islands because the product failed dissolution specifications.
Actavis is recalling 11,445 bottles of Desmopressin Acetate Tablets because some tablets are incorrectly imprinted with an X.
Mercedes-Benz is recalling specific 2015 and 2016 models because a damaged seal may fall into the engine bay, increasing the risk of a fire.
Create Common Good is recalling approximately 185 pounds of jambalaya products due to misbranding and undeclared allergens, including milk and beef.
Mitsubishi Fuso is recalling certain FEC52, FEC72, and FEC92 trucks because brake pad shims may rust, increasing stopping distance and crash risk.
Breezer is recalling about 1,700 Downtown bicycles because pedals can separate from the spindle, posing a crash hazard. No injuries have been reported.
Britax is recalling specific ClickTight child seats because a red harness adjuster button may stick, allowing the shoulder harness to loosen and increasing injury risk in a crash.
Strick Trailers is recalling 2013 Dry Freight Van Trailers because the tires are positioned too far forward, failing to meet federal rear impact protection standards.
Michelin is recalling specific BFGoodrich tires because a sidewall rupture in the bead area may cause rapid air loss, increasing the risk of a vehicle crash.
Looking for a different month? Back to 2015.