Anyone who has had an injection with the suspected batch numbers/lot numbers should already have been contacted. This happened months ago and has only just hit the news. If you go to fda.gov the information is there.
Here is how it goes: Company tests batches for issues, they notice issue they contact FDA and let them know that they have a problem. The division of Biologics is the exact group at FDA involved in "injectables". The FDA then investigates the site of the contaminate. This takes lots of time to happen. At any rate physicians or facilities are notified by the supplier that they have an "incident" and they issue a recall. Somewhere along that line the press becomes aware of the goings on. If it is widespread the FDA, CDC, HHH and others setup with the company the recall. If the drug in this case an injectable medication has been used then a recall is very silly, does the patient have to be "recalled"? Well your doctor would already have notified you. Do you have anything that states what lot number was on the vial you were injected with? Your doctor does and you need to call ASAP. This is not something to play around with.
I don't know if this is your problem, you may have an allergic reaction to the medication. My mother and sister have this type of reaction to lidocaine and other ____caines. It is not topical lidocaine it is only in the injection. You may also have a problem with too much cortisone in your system. I have had this when I have had lots of injections at different doctors or when taking higher dose orally. You can have rash, feel hot like you are burning up, get chills, and suffer a little mania (which co-workers think is funny but it's not really).
Meningitis is no joke and you would suffer such a headache you would go to the ER. You would be very, very sick. Call a doctor.